| genome sequencing technologies |
provide opportunity to generate |
high-quality genome assemblies |
|
| CrusView |
enables analysis of |
segmental duplications |
|
| class II peroxidase potential estimates |
are based on |
genomes matching 50 out of 195 fungal genera |
|
| 31 candidate genes |
have orthologous genes in |
Arabidopsis thaliana |
Brassica rapa; Arabidopsis thaliana |
| close relatedness of Rorippa species to Arabidopsis |
allowed use of |
DNA microarrays developed for Arabidopsis model species |
Rorippa amphibia; Rorippa sylvestris; Arabidopsis thaliana |
| CrusView |
enables analysis of |
genomic macrosynteny |
|
| genes strongly differentially regulated in garden cress seed compartments |
were also strongly regulated in |
Arabidopsis in similar manner in same compartments |
Lepidium sativum; Arabidopsis thaliana |
| CrusView |
includes array of utilities to visualize |
genome synteny |
|
| core genomes of multiple introductions |
are highly similar |
each other |
Magnaporthe oryzae |
| synteny plots |
can be generated at scale of |
single gene to one chromosome |
|
| phylogenomics |
inferred |
gene families for 28 sequenced model species of the Plantae |
|
| Easyfig |
is used to generate |
synteny plots of genome segments |
|
| overcoming the redundancy barrier in functional studies |
could enable improving |
inferences about cell-type homologies across genetic backgrounds and species |
|
| CoGe's SynMap2 tool |
was used to assess |
synteny between Syntrichia ruralis and Syntrichia caninervis |
Syntrichia ruralis; Syntrichia caninervis |
| barley (Hordeum vulgare) |
used in comparison with |
fern species Ceratopteris richardii and Polypodium vulgare |
Hordeum vulgare; Ceratopteris richardii; Polypodium vulgare |
| study of wild relatives of Arabidopsis |
extends |
range of natural variation that can be studied |
Arabidopsis thaliana |
| CrusView |
includes array of utilities to visualize |
duplication events |
|
| CrusView |
enables analysis of |
gene families |
|
| CrusView |
is designed to facilitate |
comparative genomics research |
|
| collinearity |
was conserved between |
pea, M. truncatula, G. max and A. thaliana |
Pisum sativum; Medicago truncatula; Glycine max; Arabidopsis thaliana |
| 15 wheat varieties with publicly available genome assemblies |
three present in |
variety panel |
Triticum aestivum |
| CoGe database |
allows users to perform |
online visual analyses of genome synteny and duplication events |
|
| PLAZA |
is |
Web-based database |
|
| VISTA |
is |
Web-based database |
|
| ChIP-seq analysis |
revealed |
high degree of conservation of (AN3, ATGIF1, GIF, GIF1, AT5G28640) target genes |
|
| homology search against pea genomic sequence data from cultivar Cameor |
identified |
two sequences similar to PALM1 |
Pisum sativum |
| CrusView |
enables analysis of |
high-frequency recombination sites |
|
| genomic resources of Brassicaceae species |
have opened |
new era of comparative genomics in Brassicaceae |
|
| CoGe |
is |
comparative genomics analysis platform |
|
| genes of interest |
are associated with |
syntenic regions |
|
| clusters of orthologs |
provide |
phylogenomic framework for in-depth and genome-wide comparative analysis |
|
| potato genome search |
identified |
StCLV2 |
Solanum tuberosum |
| 2 081 674 variants |
were located in |
genic regions (27.5%) |
Ficus erecta; Ficus carica |
| discrepancy between human and Arabidopsis SNP density patterns |
may require |
another independent investigation |
|
| (ATMED14, MED14, SWP, AT3G04740) paralogues |
are present in |
animals, plants, fungi and protozoa |
|
| Ory s 23 and (CYN, AT3G23490) d 23 |
show amino acid identity of |
37% amino acid identity with 55% positives |
Oryza sativa; Cynodon dactylon |
| CrusView karyotype feature |
may facilitate understanding of |
chromosome evolution |
|
| CrusView |
is more flexible than database-based comparative genomics tools in ability to analyze |
unpublished genomes |
|
| CrusView |
may be used in |
other organisms |
|
| barley |
is |
Poaceae genome comparison reference |
|
| CrusView |
may be used in |
other plant families |
|
| photoautotrophic eukaryotes |
have |
sequenced genomes |
|
| homologous gene pairs |
identified by |
sequence similarity |
Salicornia parvula; Arabidopsis thaliana |
| A candidate for the fig sex determinant gene |
is |
an orthologue of RESPONSIVE-TO-ANTAGONIST1 (AtHMP51, HMA7, RAN1, AT5G44790) in Arabidopsis |
Ficus carica; Arabidopsis thaliana |
| 387 alpha-gliadin peptide variants |
includes |
27 peptide variants present in both T. aestivum and A. tauschii |
Triticum aestivum; Aegilops tauschii |
| 2946 OGs |
include proteins of |
Brassicaceae |
Aethionema arabicum; Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum |
| 89.3% of genes in OGs shared with other species in Ae. arabicum |
is compared to |
92.4% on average in the other Brassicaceae, and only 64.9% in papaya |
Aethionema arabicum; Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum; Carica papaya |
| COP data |
enabled characterization of |
genome structure of eight species |
Cucumis |
| new whole-genome comparisons enabled by improved assembly methods |
reveal and utilize essentially all |
differences between genomes independent of their size or complexity |
|
| Brachypodium distachyon |
is |
Poaceae genome comparison reference |
Brachypodium distachyon |
| N. attenuata and N. obtusifolia gene sets |
were included in |
parental origin analysis of N. benthamiana |
Nicotiana attenuata; Nicotiana obtusifolia |
| 5 477 434 variants |
were located in |
intergenic regions (72.5%) |
Ficus erecta; Ficus carica |
| Acer truncatum, Camellia sinensis, Gossypium raimondii, Arabidopsis thaliana, and Acer yangbiense |
share |
10 033 gene clusters |
Acer truncatum; Camellia sinensis; Gossypium raimondii; Arabidopsis thaliana; Acer yangbiense |
| Aethionema arabicum gene annotation |
is valuable resource for |
comparative genomics analyses |
Aethionema arabicum |
| 1372 OGs |
include |
Brassicaceae except for Ae. arabicum |
Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum |
| k-mer frequency ratio analysis |
was used to analyze |
171 million Illumina 101 bp paired-end reads of Aegilops speltoides |
Aegilops speltoides |
| tandem duplicates in Ae. arabicum |
is significantly lower than in |
A. thaliana (with 10 390) |
Aethionema arabicum; Arabidopsis thaliana |
| A. tauschii lines Ent-077 and Ent-078 |
have peptide variant expression pattern most similar to |
bread wheat lines |
Aegilops tauschii; Triticum aestivum |
| 13.84% of the genes |
were classified as |
both At-α ohnologs and tandem duplicates |
Arabidopsis thaliana; Aethionema arabicum |
| collinear blocks on Amaranthus hypochondriacus |
most have |
one or two homoeologous copies in Amaranthus cruentus |
Amaranthus cruentus; Amaranthus hypochondriacus |
| s01133g27051 and s01133g27052 |
had |
40 and 72 missense mutations respectively |
Ficus carica |
| X. viscosa genome |
was searched for |
similar sequences to X. humilis (ABI3, AtABI3, SIS10, AT3G24650) |
Xerophyta viscosa |
| six diploid Nicotiana species |
were analyzed for homologues of |
genes of Nicotiana benthamiana and Nicotiana tabacum |
Nicotiana benthamiana; Nicotiana tabacum; six diploid Nicotiana species |
| 18 616 gene groups |
include |
109 single-copy gene families |
Acer truncatum |
| (LEA, AT2G21490) genes in Acer truncatum (82 genes) |
is more than |
(LEA, AT2G21490) genes in Arabidopsis thaliana (50), Camellia sinensis (72), Moringa oleifera (55), Acer yangbiense (68), Solanum lycopersicum (74) |
Acer truncatum; Arabidopsis thaliana; Camellia sinensis; Moringa oleifera; Acer yangbiense; Solanum lycopersicum |
| 387 alpha-gliadin peptide variants |
includes |
211 peptide variants unique to T. aestivum |
Triticum aestivum |
| species that diverged less time ago |
have more similarity in |
their gene composition |
Aethionema arabicum; Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum; Carica papaya |
| Ae. arabicum |
had |
5357 tandem duplicates |
Aethionema arabicum |
| rice GTs |
computationally identified as rice-diverged by detecting which |
rice GTs lack orthologs in sequenced dicots |
Oryza sativa; Arabidopsis thaliana; Populus trichocarpa; Medicago truncatula; Ricinus communis |
| five genes in O2 region and one in (OHP, OHP1, PDE335, AT5G02120) region |
conserved between |
sorghum and maize |
Sorghum bicolor; Zea mays |
| phylogenetic analysis |
included |
12 grapevine sequences and 76 sequences from representative dicot and monocot species |
Vitis vinifera; Arabidopsis thaliana; Populus trichocarpa; Solanum lycopersicum; Picea abies; Pinus sitchensis; Pinus sylvestris; Citrus sinensis; Oryza sativa; Zea mays |
| published sulfate transporter genes |
from |
different plant species |
|
| m6A methylation patterns in plant mitochondria |
differ markedly from |
m6A patterns in bacteria |
Arabidopsis thaliana; Brassica oleracea var. botrytis |
| compare feature |
has power to reveal |
candidate sequences with increased multiplicity or uniqueness to compared WGS datasets |
|
| Venn diagram of orthogroups |
showed concordance with |
topology of the species' phylogenetic tree |
Aethionema arabicum; Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum; Carica papaya |
| approach and data resources created in this study |
could be easily expanded to |
other plant systems |
|
| 74.03% of the genes with more copies in A. thaliana and one copy in Ae. arabicum |
were classified as |
At-α ohnologs or tandem duplicates |
Arabidopsis thaliana; Aethionema arabicum |
| Kmasker plants compare mode analysis of barley cultivar Morex gene set |
using |
two WGS datasets of spring and winter barley |
Hordeum vulgare |
| 62 A. thaliana genes |
could be divided into |
45 orthogroups |
Arabidopsis thaliana; Xerophyta viscosa |
| comparative analysis |
was completed with |
five other plant species with annotated genomes |
Arabidopsis thaliana; Camellia sinensis; Moringa oleifera; Acer yangbiense; Solanum lycopersicum |
| phylogenetic heatmap |
is based on |
2,617 phylogenetic trees and eight tissue RNA-sequencing datasets |
Oryza sativa L. |
| mapped F. carica contigs |
covered |
193 530 279 bp |
Ficus carica |
| newly assembled genomes |
provided opportunity for |
identifying SVs and understanding genome evolution |
Oryza nivara; Oryza rufipogon; Oryza barthii; Oryza glaberrima |
| number of common orthogroups (OGs) |
decreases in accordance with |
divergence time of the species |
Aethionema arabicum; Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum; Carica papaya |
| divergence of the genus Aethionema |
occurred after |
the 'crown group' of Brassicaceae |
Aethionema arabicum |
| three of 11 amino acids in motifs |
are conserved in |
Lhcx4 compared with Lhcx1 |
Phaeodactylum tricornutum |
| phylogenetic profiling |
identifies |
functionally linked proteins |
|
| Acer truncatum and Camellia sinensis |
have |
396 syntenic blocks with 1:1 syntenic patterns (cscore >0.7) |
Acer truncatum; Camellia sinensis |
| 33-mer peptide |
was not found in |
A. tauschii in earlier studies |
Aegilops tauschii |
| MCScanX analysis |
examined |
homologous relationships among the 17 Amaranthus cruentus pseudochromosomes |
Amaranthus cruentus |
| methods to analyze sets of assemblies |
are hardly available |
|
|
| m6A-RIP-seq data |
provided |
similar m6A patterns |
Arabidopsis thaliana; Brassica oleracea var. botrytis |
| Cross-mapping of fsQTLs between bottle gourd and relatives |
revealed |
syntenic relationship of bottle gourd fsQTLs with 12 fsQTLs in cucumber, melon or watermelon |
|
| gene manipulation tools |
have driven |
mustard species into the spotlight of comparative research |
|
| Carica papaya (Brassicales) |
has a higher number of |
exclusive genes (3559), exclusive OGs (844) and unassigned genes (6200) |
Carica papaya |
| genome sequencing |
provides |
insights into evolution and function of BAHD acyltransferases |
|
| research with Arabidopsis thaliana |
can be complemented by investigating |
other plants with larger, more complex genomes |
Arabidopsis thaliana |
| Brassicaceae species |
showed in 20.7% of the cases that |
many genes were orthologs of only one gene in Ae. arabicum |
Aethionema arabicum; Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum |
| networks |
are becoming available for |
various plant species |
|
| four Lhcx protein sequences of Phaeodactylum tricornutum |
were aligned and searched for |
major differences between Lhcx1/2/3 and Lhcx4 proteins |
Phaeodactylum tricornutum |
| Cucumber Chr07 |
is syntenic to |
CM27 (ATDDM1, CHA1, CHR01, CHR1, DDM1, SOM1, SOM4, AT5G66750) |
Cucumis sativus; Cucumis metuliferus |
| MCScanx analysis of Amaranthus cruentus and Beta vulgaris |
confirmed |
13 963 collinear genes |
Amaranthus cruentus; Beta vulgaris |
| metal hyperaccumulation and hypertolerance research |
provides |
highly relevant framework for comparative genomics |
|
| additional wheat varieties |
allow examination of |
copy number variation |
Triticum durum; Triticum aestivum |
| genomes of pathogenic and saprobic fungi |
comparison with |
ectomycorrhizal Laccaria genome |
Laccaria |
| Ancestral Crucifer Karyotype (ACK) and genomic blocks |
is |
robust model |
|
| clustering |
is explored to |
identify functionally equivalent genes |
|
| plant homologues (orthologues) |
are deduced from |
mammalian counterparts |
|
| OsCAS |
is aligned with |
AtCAS from Arabidopsis |
Oryza sativa; Arabidopsis thaliana |
| genome-wide atlas of conserved noncoding sequences (CNSs) |
illustrates power of |
comparative approaches |
|
| homologous gene families |
can be tested for functional conservation across |
major plant lineages |
|
| comparative analysis of multiple plant and non-plant genomes |
led to |
identification of genes specific for and conserved in cp-containing photosynthetic organisms |
|
| k-mer size upwards of k = 20 |
should be considered for |
dissimilarities between related and complex species |
|
| active QTLs-alleles in population changes |
were identified |
through direct comparisons among QTL-allele submatrices |
Glycine max |
| collinear blocks on Amaranthus hypochondriacus and Amaranthus cruentus |
indicate |
predominant 1:1 relationship with translocations of a number of collinear blocks |
Amaranthus cruentus; Amaranthus hypochondriacus |
| NBS-LRR gene number between Cucumis metuliferus CM27 and Cucumis melo L. ssp. agrestis IVF77 |
is significant |
P < 0.01 |
Cucumis metuliferus; Cucumis melo |
| Investigations of the algal relatives of land plants |
have strongly benefitted from |
recent progress in phylogenomics on plants and algae |
|
| 25 genomes |
include |
seven magnoliids, eight eudicots, six monocots, two angiosperm basal group species, and two gymnosperms |
|
| Cucumis metuliferus CM27 and Cucumis melo L. ssp. agrestis IVF77 genomes |
contain |
7,719 inversions (>1 kb) and 4,710 intra-translocations (>1 kb) |
Cucumis metuliferus; Cucumis melo |
| Cucumber Chr06 |
is syntenic with genomic regions of |
CM27 Chr03, Chr08 and (CHR11, AT3G06400) |
Cucumis sativus; Cucumis metuliferus |
| accumulating genomic information |
provides opportunity to perform |
comparative analyses |
|
| cucumber oligonucleotide (oligo) pools |
allowed |
56 genome blocks in Cucumis to be distinguished |
Cucumis sativus; Cucumis |
| many other dioecious desert plants |
have been subject of |
genetic research |
|
| 5′-UTR sequences from 22 species in Embryophyta |
were aligned to extract |
sequences in positions relevant to AUG-stop in Arabidopsis thaliana |
Arabidopsis thaliana; Embryophyta |
| genome sequencing of barley, wheat, and the diploid A and D progenitor genomes of wheat, as well as rye and diploid Th. elongatum |
has enabled |
genome-wide comparative sequence analyses of introgressive hybridization among Triticeae species |
|
| predicted protein-CDS in Amaranthus cruentus |
greater proportion had |
longer sequence compared with Amaranthus hypochondriacus |
Amaranthus cruentus; Amaranthus hypochondriacus |
| Arabidopsis thaliana (dicot) |
is used as |
model plant taxa for comparative study |
Arabidopsis thaliana |
| Cucumis melo L. ssp. agrestis IVF77 |
shows genomic collinearity with |
DHL92 melon genome |
Cucumis melo |
| large intra-chromosomal translocation on Chr05 |
can be detected when comparing |
thin-skinned melons (IVF77 and DHL92) with thick-skinned Payzawat |
Cucumis melo |
| methods to analyze sets of assemblies |
might change soon and open door for |
analyses of entire genomes of large panels of plants |
|
| low-resolution whole-chromosome painting |
reveal at macro level |
syntenic relationships of related species |
|
| Cafe software |
was used to identify |
gene families expanded or contracted across 14 genomes |
14 angiosperm species |
| (ATBRI1, BIN1, BRI1, CBB2, DWF2, AT4G39400) ATG-stop conservation |
was conserved in |
9 out of 22 organisms |
Arabidopsis thaliana; Embryophyta |
| plant pangenomes |
have expanded to encompass |
multiple related species at the genus level |
|
| BLASTN query with wheat nucleotide sequence |
resulted in |
single highly significant (e <10 −6 ) result at nucleotide level for Brachypodium |
Triticum aestivum; Brachypodium distachyon |
| around one-third of Y1 and Y2 insertion sequences |
were unique with homologues not found in |
other organisms |
Simmondsia chinensis |
| ATG-stops in NIP5;1 |
were more highly conserved among plant species than |
flanking regions in 5′-UTR |
Arabidopsis thaliana; Embryophyta |
| comparative genomic analyses |
largely rely on |
linear visualizations between genomes |
|
| 24 792 of 27 995 contigs of F. carica genome |
were mapped onto |
F. erecta pseudomolecule sequences |
Ficus erecta; Ficus carica |
| m6A methylation patterns in plant mitochondria |
differ markedly from |
m6A patterns in nuclear-encoded mRNAs in eukaryotes |
Arabidopsis thaliana; Brassica oleracea var. botrytis |
| VvWOX1 and VvWOX6 genes |
are correlated in |
exon structure and peptide motif |
Vitis vinifera |
| genomic comparisons with phylogenetic analysis |
allows |
gene identification |
|
| relative importance of four genetic factors |
was evaluated through |
direct comparisons among QTL-allele submatrices |
Glycine max |
| most closely related sequences |
were from |
beetroot, quinoa, and spinach |
Simmondsia chinensis |
| Cucumber Chr02 |
is syntenic with genomic regions of |
CM27 Chr03, Chr05 and (CHR11, AT3G06400) |
Cucumis sativus; Cucumis metuliferus |
| first AUG-UAA in NIP5;1 |
was conserved in |
21 out of 22 species tested |
Arabidopsis thaliana; Embryophyta |
| C. rubella |
has a similar number of |
exclusive OGs (244) |
Capsella rubella |
| A. cruentus genome assembly (371 Mb) |
is slightly shorter than |
latest A. hypochondriacus genome assembly (404 Mb) |
Amaranthus cruentus; Amaranthus hypochondriacus |
| genome sequences |
enabled |
comparative quantitative proteomic and transcriptomic analyses |
Arabidopsis thaliana; Oryza sativa; Populus trichocarpa; Sorghum bicolor; Zea mays |
| foundational resources for Oryza genus |
includes |
reference genomes and transcriptomes for all 23 Oryza species |
Oryza |
| regions on maize chromosomes 2 and 5 from second round of WGD duplications |
are almost 5.5 times smaller than |
regions on other maize chromosomes |
Zea mays |
| Inparanoid Version 2.0 |
used to identify |
rice GT orthologs in sequenced dicots |
Oryza sativa; Arabidopsis thaliana; Populus trichocarpa; Medicago truncatula; Ricinus communis |
| H. glycines parasitism genes |
only about 30% have |
database orthologues |
Heterodera glycines |
| Brachypodium genome and accompanying resources |
should provide |
more relevant model for temperate cereals |
Brachypodium distachyon |
| genome segment between 6–10Mb on rice chromosome 3 |
aligns with |
16 rice QTLs for traits related to drought response |
Oryza sativa |
| 28 OsDof genes |
exhibited |
strong consistency in ordering along the chromosomes |
Oryza sativa; Sorghum bicolor |
| entire blocks on chromosome 02A and 02B in Amaranthus cruentus |
share collinearity with |
chromosome 2 in Amaranthus hypochondriacus |
Amaranthus cruentus; Amaranthus hypochondriacus |
| isolation of genes underlying orthologous traits |
is the first step in conducting |
comparative functional studies |
|
| TB unigene set |
corresponded to |
potato and/or tomato unigene sets |
Solanum torvum; Solanum tuberosum; Solanum lycopersicum |
| VvRopGEFs |
were named according to |
their sequence similarity to AtRopGEFs from Arabidopsis thaliana |
Vitis vinifera; Arabidopsis thaliana |
| maize myosins |
average size much larger than |
rice myosins |
Zea mays; Oryza sativa |
| functional genomic data |
are not easily integrated for comparison between and within |
different rice GT families |
Oryza sativa |
| naphthoate synthase (NS/ (DHNS, ECHID, AT1G60550) ) |
is |
single orthologue of cyanobacterial MenB |
Arabidopsis thaliana; cyanobacteria |
| Arabidopsis thaliana |
is studied in comparative analysis with |
Capsella rubella and Cardamine hirsuta |
Arabidopsis thaliana; Capsella rubella; Cardamine hirsuta |
| region containing O2 on maize chromosome 7S |
is twice the size of |
region containing (OHP, OHP1, PDE335, AT5G02120) on maize chromosome 1 |
Zea mays |
| large intra-chromosomal translocation on Chr05 |
cannot be detected when comparing |
IVF77 with DHL92 |
Cucumis melo |
| Cucumber Chr05 |
is syntenic with genomic regions of |
CM27 Chr09 and (ASG3, CHR10, AT2G44980) |
Cucumis sativus; Cucumis metuliferus |
| evolution at chromosome level of A. hypochondriacus |
compared with |
quinoa and sugar beet |
Amaranthus hypochondriacus; Chenopodium quinoa; Beta vulgaris |
| 454 388 genes from 14 genomes |
78.8% could be assigned to |
orthogroups (21 039 orthogroups) |
14 angiosperm species |
| genome duplications |
cause |
orthology issues |
|
| phylogenetic trees |
provide context to compare |
properties of gene family members |
|
| 2944 pOGs |
comprise |
34% of 8714 total pOGs |
Solanum tuberosum; Arabidopsis thaliana |
| GDIs from Citrus sinensis, Malus × domestica, and Solanum lycopersicum |
were generally the most abundant series |
in these species |
Citrus sinensis; Malus × domestica; Solanum lycopersicum |
| histone H4 and BdGLO2 |
have |
more than one homologue |
Brachypodium distachyon |
| A. thaliana genes in many-to-one OGs |
were found to be |
ohnologs (homeologs) derived from the At-α WGD in 38.87% of the cases |
Arabidopsis thaliana |
| genes, proteins and metabolites |
are similarly affected across |
different resurrection plant species |
|
| OBF-BINDING PROTEIN 3 ( (OBP3, AT3G55370) ) |
had |
relatively high ATG-stop conservation ratios |
Arabidopsis thaliana; Embryophyta |
| intragenomic duplications |
can be integrated with |
intergenomic colinearity data |
|
| papaya lcy-β2 amino acid sequences |
was aligned with |
tomato and arabidopsis lycopene β- and ϵ-cyclases |
Carica papaya; Solanum lycopersicum; Arabidopsis thaliana |
| cross-species microarray hybridization |
can be used for |
applying model organism genomics in related species for which few functional genomics resources are available |
|
| naphthoate synthase (NS) |
is |
orthologous to MenB from cyanobacteria, chlorobi, and red algae |
Arabidopsis thaliana; cyanobacteria; chlorobi; red algae |
| BLASTN survey of wheat endosperm- and cell type-specific genes against Brachypodium genome |
revealed |
generally lower levels of sequence similarity in grouping expressed in aleurone layers |
Triticum aestivum; Brachypodium distachyon |
| BdGLO2 |
is |
member of family of genes related to 12S globulins of oat |
Brachypodium distachyon; Avena sativa |
| Carica papaya (Brassicales) |
is sister to |
Brassicaceae |
Carica papaya |
| Brassicaceae species |
showed in 5.8% of the cases that |
a single gene corresponds to many in Ae. arabicum |
Aethionema arabicum; Arabidopsis thaliana; Capsella rubella; Eutrema salsugineum |
| critical gaps in the land plant tree of life |
have been filled |
recent publications of genomes of liverworts, ferns and hornworts |
|
| predicted protein-CDS in Amaranthus cruentus and Amaranthus hypochondriacus |
vast majority were |
the same length in both species |
Amaranthus cruentus; Amaranthus hypochondriacus |
| MCScanX analysis |
found |
4561 collinear genes |
Amaranthus cruentus |
| MCScanx analysis of Amaranthus cruentus and Amaranthus hypochondriacus |
identified |
35 242 collinear genes representing 74% and 71% of the Amaranthus hypochondriacus and Amaranthus cruentus gene complements, respectively |
Amaranthus cruentus; Amaranthus hypochondriacus |
| moss genome sequencing |
enabled |
inference of ancestral land plant states |
|
| 229 genes |
showed high degree of homology to |
corresponding Arabidopsis gene products at amino acid sequence level |
Gossypium hirsutum; Arabidopsis thaliana |
| proximity of (bHLH, AT5G51780) genes more distantly related to OsRHL1 to the 5AL locus |
may simply be |
coincidental |
|
| Inparanoid |
is |
automated method for finding orthologs and in-paralogs from two species |
|
| three different proteins orthologous to (ATWOX13, HB-4, WOX13, AT4G35550) |
were identified in |
grapevine |
Vitis vinifera |
| detailed comparisons with extremophile ARMS |
should reveal |
active functional sites within C-terminus of (ATNHX7, ATSOS1, SOS1, AT2G01980) |
halophytes |
| monocots |
only one in |
(ATXIK, XI-17, XI-K, XIK, AT5G20490) and XI-E |
Zea mays; Oryza sativa; Sorghum bicolor |
| scripts in DiagHunter/GenoPix2D distribution |
produce |
finished images and predictions of synteny blocks |
|
| BLAST searches of the Brachypodium genomic sequence |
identified |
corresponding interval of 198 kb on Brachypodium chromosome 2 |
Brachypodium distachyon |
| genomic sequences of salt cress and Thellungiella parvula |
will enhance |
identification of genes responsible for salt tolerance |
Thellungiella salsuginea; Thellungiella parvula |
| MUMmer |
is used for |
identifying regions of homology between genomes |
|
| parsed BLAST data generation |
includes |
underlying BLAST analysis |
|
| RFLP probes mapped to the HvNax4 region |
identified |
related genomic region on the long arm of rice chromosome 5 |
Hordeum vulgare; Oryza sativa |
| barley orthologues of metal homeostasis genes |
obtained by |
BLAST search against TIGR Barley Gene Indices |
Hordeum vulgare |
| 8714 pOGs |
include |
18,420 S. tuberosum ESTs and 14,647 A. thaliana protein-coding genes |
Solanum tuberosum; Arabidopsis thaliana |
| phylogenetic distance of transformable C4 species from A. thaliana |
means that direct comparison with |
most widely studied model plant |
Arabidopsis thaliana |
| combining high-throughput sequencing and microarray technologies |
will serve as basis for |
future comparative functional genomic analyses using syntenic orthologues |
Populus euphratica; Populus trichocarpa |
| OrthoMCL |
requires |
assumptions about similarities |
|
| BR2/ZmABCB1 locus |
lies in a region syntenous to |
OsABCB22 |
Zea mays; Oryza sativa |
| OsCAS |
is aligned with |
BpCAS from birch |
Oryza sativa; Betula pendula |
| Arabidopsis; salt cress |
displayed high DNA sequence identity of |
90–95% for majority of transcripts |
Arabidopsis thaliana; Thellungiella salsuginea |
| VvWOX13B and VvWOX13C |
have very similar sequences with |
94% nucleotide identity |
Vitis vinifera |
| O2 region |
aligned with |
orthologous region in sorghum |
Oryza sativa; Sorghum bicolor |
| (OHP, OHP1, PDE335, AT5G02120) region |
aligned with |
orthologous region in sorghum |
Oryza sativa; Sorghum bicolor |
| homeodomain sequences |
aligned using |
MUSCLE algorithm |
Physcomitrium patens; Marchantia polymorpha; Selaginella moellendorffii; Ceratopteris richardii; Salvinia cucullata; Azolla filiculoides; Sequoiadendron giganteum; Oryza sativa; Populus trichocarpa; Arabidopsis thaliana |
| KOGs |
reports |
size of the conserved core of eukaryotic genes |
|
| gene set |
could be used successfully to |
identify syntenic blocks with sequenced rosid species |
Beta vulgaris |
| CrusView |
is designed for |
visualized analyses of comparative genomics data |
|
| self-defined genomic information |
can be integrated with |
genomic synteny maps |
|
| CrusView |
enables analysis of |
chromosomal rearrangements |
|
| sequence variations in C-terminal region of (ATNHX7, ATSOS1, SOS1, AT2G01980) |
are much more pronounced than variations in |
N-terminus |
Arabidopsis thaliana; halophytes |
| number of full-length (TPL, WSIP1, AT1G15750) genes in tomato |
fell in the range found in |
other plant genomes |
Solanum lycopersicon |
| phyletic pattern |
is |
a central notion introduced in the context of the COG analysis |
|
| study |
included in analysis |
(CBP1, MEE14, AT2G15890) from silkworm Bombyx mori |
Bombyx mori |
| Ceratodon purpureus |
has |
U and V sex chromosomes that share no obviously syntenic regions with each other |
Ceratodon purpureus |
| genoPlotR |
is used to generate |
synteny plots of genome segments |
|
| 92,668 genes of 'ZS11' (91%) |
could be clustered into |
OrthoMCL gene families |
Brassica napus |
| maize myosin genes |
number comparable to |
rice myosin genes |
Zea mays; Oryza sativa |
| 59 LTR-RTs and 145 DNA (ATNACK2, NACK2, TES, AT3G43210) present in assembled Brassica oleracea sequences |
were found as intact or truncated elements in |
assembled Brassica rapa sequences |
Brassica rapa; Brassica oleracea |
| some (ATNACK2, NACK2, TES, AT3G43210) shared by the two genomes |
may not be detected based on |
comparison of assembled sequences |
Brassica rapa; Brassica oleracea |
| whole-genome bisulfite sequencing (WGBS) and RNA sequencing |
were used to evaluate |
DNA methylation and gene expression differences in poplar and the fungus |
Populus spp.; Laccaria bicolor |
| of the 931 attdf1 downregulated genes |
only 99 genes were also only downregulated in |
HvTDF1 |
Arabidopsis thaliana; Hordeum vulgare |
| melon family members of six cloned tomato QTLs |
were identified in |
melon genome sequence |
Cucumis melo |
| 229 cotton ESTs (expressed sequence tags) |
correspond to |
232 Arabidopsis candidate genes |
Gossypium hirsutum; Arabidopsis thaliana |
| genes in BrSIO2 region |
have |
243 homologues in A. thaliana |
Brassica rapa; Arabidopsis thaliana |
| large difference in genome size, structure, and dynamics between Arabidopsis thaliana and most crop species |
may be a challenge for |
transferring knowledge from Arabidopsis to crop species |
Arabidopsis thaliana |
| this review |
highlights convergence or differences existing with |
crops |
|
| programs designed to work with nucleotide data |
may not work with |
peptide data |
|
| Panicum hallii transcripts |
compared with |
Setaria italica gene models |
Panicum hallii; Setaria italica |
| synteny among species of the Triticeae tribe and whole Poaceae family |
makes genomic mapping and sequence information highly transferable across |
species |
|
| substantial colinearity evident from comparing group 7 wheat versus Th. ponticum genetic maps |
supports |
reasonable hypothesis of the existence of multiple yield-contributing loci along the 7L arms of both species |
Triticum aestivum; Thinopyrum ponticum |
| 121 annotated genes in BrSIO1 |
have |
103 homologues in Arabidopsis thaliana |
Brassica rapa; Arabidopsis thaliana |
| positions of the homologues identified from the BLAST search |
were compared with |
positions of markers in the region of the QTL |
|
| contigs containing OsRHL1 homologues |
were located near |
markers |
|
| Sonnhammer and co-workers |
applied the methodology to |
the sequenced eukaryotic genomes |
|
| genome-scale comparisons of internal duplications in the Arabidopsis thaliana genome |
depended on |
custom bioinformatics efforts and extensive pre- and post-processing tailored to the Arabidopsis genome |
Arabidopsis thaliana |
| TC141300 |
showed |
48% amino acid identity and 68% similarity to (CYP82C2, AT4G31970) |
Gossypium hirsutum; Arabidopsis thaliana |
| substantial colinearity |
emerged from |
wheat 7AL versus Th. ponticum 7AgL genetic map comparison |
Triticum aestivum; Thinopyrum ponticum |
| maize myosin genes |
number less than |
Arabidopsis myosin genes |
Zea mays; Arabidopsis thaliana |
| chromosome-to-chromosome synteny relationships |
enabled production of |
partial wheat gene-based physical map (syntenome) with 17,317 COS |
Triticum aestivum; Oryza sativa; Sorghum bicolor; Brachypodium distachyon; Zea mays |
| Physcomitrella patens expression data |
enables |
cross-species comparisons of gene expression among photosynthetically active species |
Physcomitrella patens |
| genes in 'ZS11' |
were homologous to |
genes in Brassica rapa (Ar), Brassica oleracea (Co), Brassica napus 'Darmor-bzh', and Arabidopsis thaliana (97.35%) |
Brassica napus; Brassica rapa; Brassica oleracea; Arabidopsis thaliana |
| FISH in cucumber |
has been used successfully for |
comparative mapping with melon |
Cucumis sativus |
| 25 genes |
are collinear between |
two genomes |
Oryza sativa; Brachypodium distachyon |
| de novo assembly of BSA derived RenSeq data |
used as |
genotype-specific reference |
|
| five pairwise tBLASTn comparisons |
performed between |
pennycress and each of five Brassicaceae species |
Thlaspi arvense; Arabidopsis thaliana; Arabidopsis lyrata; Brassica rapa; Capsella rubella; Thellungiella halophila |
| ps-2 locus region |
shows synteny with |
Arabidopsis thaliana |
Solanum lycopersicum; Arabidopsis thaliana |
| transcriptome and metabolome analysis |
revealed |
differences in transcripts and metabolites between Regent and Trincadeira |
Vitis vinifera |
| genes identified in Arabidopsis following infection with three pathogens |
were used to |
isolate homologues genes in cotton |
Gossypium hirsutum |
| Perennial ryegrass (Lolium perenne L.) |
shares significant synteny with |
other grass species |
Lolium perenne L. |
| Poaceae species |
exhibit high synteny at macro level |
genome organization |
|
| markers in region associated with LG4 QTL in perennial ryegrass (pps0040 and lpssr006) |
were aligned by in silico comparative analysis to |
genome segment between 6–10Mb on rice chromosome 3 |
Oryza sativa |
| sequence identity profiles and phylogenic relationships |
grouped chromosome blocks into |
two distinct clusters |
Aegilops markgrafii |
| single member of CrRLK1L family in M. polymorpha |
is more similar to |
AtTHE than to any other A. thaliana protein in this family |
Marchantia polymorpha; Arabidopsis thaliana |
| matrices of collinear genes and rearrangements |
were constructed from |
homology search results |
Aegilops tauschii; Triticum turgidum subsp. dicoccoides; Brachypodium distachyon; Sorghum bicolor; Oryza sativa |
| uncertainty about which orthologue retains the same function as the corresponding gene in the model species |
is a consequence of |
presence of multiple orthologues |
|
| A. lyrata and A. thaliana genomes |
could be easily aligned |
each other |
Arabidopsis lyrata; Arabidopsis thaliana |
| A. thaliana chromosome 4 centromere |
corresponds to syntenic region in |
A. lyrata chromosome 4 centromere |
Arabidopsis thaliana; Arabidopsis lyrata |
| Thellungiella parvula contigs |
aligned with |
chromosome A3 of Brassica rapa |
Thellungiella parvula; Brassica rapa |
| 9,119 genes |
comprised |
genus-wide alignments for 25 Mb of genome |
Arabidopsis thaliana |
| this study |
compared |
genomes of three potato species |
Solanum chacoense; Solanum tuberosum; Solanum commersonii |
| M. polymorpha PTI protein |
is sister to |
group of six A. thaliana PTI proteins that includes MARIS |
Marchantia polymorpha; Arabidopsis thaliana |
| ortholog and phylogenetic analyses |
were conducted and yielded results |
consistent with previous studies |
Prunus persica |
| DiagHunter |
assigns numbers |
synteny blocks |
|
| scripts in DiagHunter/GenoPix2D distribution |
allow processing of |
The Institute for Genomic Research (TIGR) pseudochromosome assemblies |
|
| high-throughput technologies |
facilitate |
comparative analyses across species |
|
| GeneChip microarray studies |
demonstrated potentials in |
studies of closely related species |
Arabidopsis thaliana; Arabidopsis halleri |
| DiagHunter |
identifies |
very large-scale synteny blocks on the order of many megabases |
|
| chromosomes of the four target species |
thoroughly analyzed in |
previous studies |
Arabidopsis thaliana; Populus trichocarpa; Theobroma cacao; Vitis vinifera |
| DiagHunter |
makes |
genome-scale comparisons |
|
| GenoPix2D |
provides |
interactive viewing, querying, and plotting |
|
| genome sequences that represent the rosid or asterid lineage |
are |
available, or are in progress |
|
| understanding molecular processes and gene regulatory networks |
allows |
rapid utilization of this information into other plant species |
|
| KNOX protein sequences |
were downloaded from |
Genome Database for Rosaceae, TAIR, Sol Genomics Network and NCBI |
Fragaria vesca; Fragaria × ananassa; Arabidopsis thaliana; Solanum lycopersicum; Zea mays |
| highly repetitive heterochromatic DNA |
present |
particular challenges |
|
| three target genomes under consideration |
confirmed |
each other |
Vitis vinifera; Populus trichocarpa; Theobroma cacao |
| this work |
is |
the first systematic, genome-wide examination of the sets of orthologous genes in eukaryotes |
|
| DiagHunter |
can operate on |
marker data |
|
| 10 families |
differed in gene number between |
'ZS11' and 'Darmor-bzh' (P < 0.01) |
Brassica napus |
| GenoPix2D |
allows highlighting of |
groups of genes |
|
| SALAD homolog genes |
were identified in |
Arabidopsis thaliana and Solanum lycopersicum |
Arabidopsis thaliana; Solanum lycopersicum |
| protein sequences |
were aligned using |
Clustal Omega program |
Arabidopsis thaliana; Solanum lycopersicum; Fragaria vesca; Zea mays |
| GenoPix2D |
can view |
any other two-way genomic similarity comparisons |
|
| similar sequences of CaLUR transcription site |
were also found in |
other solanaceous species such as potato and tomato |
|
| core angiosperm genes |
were significantly enriched in |
PAE in all samples |
Solanum tuberosum |
| Cytogenetic approach |
provided a basis for |
comparative sequence analysis of discrete parts of the genome |
|
| all variants called on the T. urartu genome |
were projected onto |
genome of wild emmer wheat (Triticum turgidum spp. dicoccoides) |
Triticum urartu; Triticum turgidum spp. dicoccoides |
| Zea mays |
has |
more than 10-times larger genome |
Zea mays |
| A. lyrata and A. thaliana genomes |
have remained syntenic |
approximately 90% of the two genomes |
Arabidopsis lyrata; Arabidopsis thaliana |
| 32,986 distinct gene families |
are |
40% appearing to be dispensable |
Arabidopsis thaliana |
| longer and high quality reads at high coverage |
are believed to be very important to address |
evolutionary questions at whole-genome level |
|
| grape syntenic blocks |
85.84% contain two regions of synteny with |
sacred lotus gene set |
sacred lotus; Vitis vinifera |
| research on the heterozygosity of sweet orange |
contributes to |
comprehensive understanding of the genetic diversity of citrus or closely related species |
Citrus sinensis; Citrus |
| genome sequences of higher plants |
permits |
cross-species comparisons |
|
| sequence comparisons of prokaryotic and eukaryotic IPMDH |
suggest |
substitution of one active site residue may lead to altered substrate specificity and metabolic function |
Arabidopsis thaliana |
| Profilin query sequences |
are used to identify |
extended profilin homologs |
|
| ~53.6-kb genomic variation |
contains |
one gene (Ppe_1-Hap2G0054500) from (GCS1, HAP2, AT4G11720) |
Prunus persica |
| PatternHunter |
is used for |
identifying regions of homology between genomes |
|
| programs designed to identify homologous regions by sequence alignments |
may not excel at |
piecing together and reporting larger genomic-scale homologies |
|
| GenoPix2D |
provides |
interactive querying function |
|
| genes annotated in Aegilops tauschii pseudomolecules |
searched for homology with |
genes annotated in sorghum pseudomolecules |
Aegilops tauschii; Sorghum bicolor |
| four Spirodela syntenic blocks |
found between |
Amborella and Apostasia |
Spirodela polyrhiza; Amborella trichopoda; Apostasia shenzhenica |
| conservative approach |
will enhance |
accuracy of comparative analysis |
|
| studies of accelerated organelle genome evolution in plants |
have been limited to |
close relatives within just two groups (Geraniaceae and Silene) |
Geraniaceae; Silene |
| proteins of the four large clusters |
are homologous to |
annotated Phytophthora infestans RXLRs |
Plasmopara halstedii; Phytophthora infestans |
| 21,523 Thellungiella parvula ORFs |
of very similar lengths (80–120%) to |
putative Arabidopsis thaliana homologs |
Thellungiella parvula; Arabidopsis thaliana |
| programs designed to work with nucleotide data |
may not work with |
raw positional information such as marker positions |
|
| DiagHunter |
appears to out-perform |
PipMaker, MUMmer, FORRepeats, REPuter, BLASTZ and PatternHunter |
|
| extensive molecular resources for sugar beet |
enable |
cross-referencing to regions sequenced in other plant species |
Beta vulgaris |
| region of approximately 10 Mb in pseudomolecule 2 |
appeared to be |
inverted translocation from syntenic region of G. max chromosome 8 |
Glycine latifolia; Glycine max |
| phylogenetic distribution of putative and functionally characterized UGTs |
has been analyzed in |
27 plant genera with fully sequenced genomes |
Chlamydomonas reinhardtii; Physcomitrella patens; Selaginella moellendorffii |
| collinear gene pairs |
confirmed that intergenic regions in A. lyrata are longer than |
counterparts in A. thaliana |
Arabidopsis lyrata; Arabidopsis thaliana |
| phylogenetic analysis |
was conducted to |
assign putative functions and identify related genes in Arabidopsis thaliana |
Marchantia polymorpha; Arabidopsis thaliana |
| homology analysis |
identified |
25,849 genes from (GCS1, HAP2, AT4G11720) with homologous genes in (HAP1, MAGO, MEE63, AT1G02140) |
Prunus persica |
| allele-specific sequences at the GPA-resistant locus |
demonstrated |
~53.6-kb variation |
Prunus persica |
| inclusion of newly sequenced genomes |
should proceed at faster rate once |
KOG system is established |
|
| predicted flax genes |
aligned with |
Arabidopsis genes |
Linum usitatissimum |
| comparative analysis method |
is applicable for studying |
divergence of k-mer profiles between genomic datasets of closely related species |
|
| 4CL ligases from monocots and dicots |
have been characterized based on |
sequence identities to Arabidopsis 4CLs |
|
| Kmasker plants |
enables |
comparative studies between different cultivars or closely related species |
|
| three clustered genes (KCS_Maole_016461.T1, KCS_Maole_016463.T1, KCS_Maole_016467.T1) |
are closely related to |
three Arabidopsis thaliana KCS genes ( (KCS11, AT2G26640) (DAISY, KCS2, AT1G04220) (KCS20, AT5G43760) ) |
Moringa oleifera; Arabidopsis thaliana |
| F. vesca KNOXI genes |
were identified by |
blast against F. vesca genome |
Fragaria vesca |
| inclusion of newly sequenced genomes and other genomes |
will enable |
further, deeper studies into the functional and evolutionary patterns of eukaryotic life |
|
| regions of synteny between sugar beet and rosid species |
involves |
1400–2700 genes in the sequenced genomes of Arabidopsis, poplar, grapevine, and cacao |
Beta vulgaris; Arabidopsis thaliana; Populus trichocarpa; Vitis vinifera; Theobroma cacao |
| 93 450 predicted genes in F. erecta genome |
were clustered with |
genes of fig, mulberry, jujube, and sweet cherry |
Ficus erecta; Ficus carica; Morus species; Ziziphus jujuba; Prunus avium |
| genes annotated in rice pseudomolecules |
searched for homology with |
genes annotated in other grass pseudomolecules |
Oryza sativa |
| TaMs5-A, TaMs5-B and TaMs5-D |
are |
homoeologs |
Triticum aestivum |
| candidate UGTs |
were identified from |
genomes using stringent criteria |
|
| 124 RXLRs |
are found only in |
Plasmopara halstedii and Plasmopara viticola |
Plasmopara halstedii; Plasmopara viticola |
| 1:1:1 orthologs |
limits |
number of genes that could be assessed |
|
| analyses of gene families flanking the eight representative genomes of green plants |
provide |
in-depth insights into evolutionary genomics about green plants |
|
| junction sites of 102 LTR-RTs and 456 DNA (ATNACK2, NACK2, TES, AT3G43210) present in assembled Brassica oleracea sequences |
were found in |
Brassica rapa NGS read dataset |
Brassica rapa; Brassica oleracea |
| sweet orange reference genome |
may provide a resource for |
study of ancient genome traits of the mandarin and pummelo ancestors of sweet orange |
Citrus sinensis |
| CrusView |
enables analysis of |
tandem duplications |
|
| CrusView |
is developed using |
SWI/Swing graphics libraries |
|
| multiple alignment throughout all members of the ALMT family in Arabidopsis |
identified |
several conserved or partially conserved amino acids within the transmembrane domain |
Arabidopsis thaliana |
| CrusView |
allows users to integrate |
self-defined genomic information |
|
| CrusView |
allows users to upload |
self-defined genomic information |
|
| CrusView |
is designed to give users |
higher flexibility in analyzing currently unpublished genome data |
|
| whole genome sequencing data of Rorippa aquatica |
enables rapid identification of |
orthologs of Arabidopsis thaliana developmental regulatory genes |
Rorippa aquatica; Arabidopsis thaliana |
| homology analysis |
identified |
24,745 homologous genes in (HAP1, MAGO, MEE63, AT1G02140) |
Prunus persica |
| orthologs of Acer truncatum and 14 other sequenced plant species |
were clustered into |
18 616 gene groups |
Acer truncatum |
| pairwise comparison of Syntrichia ruralis and Syntrichia caninervis |
uncovered |
chromosome rearrangement between Syntrichia ruralis Chr. 11 and Syntrichia caninervis chromosomes 2 and 8 |
Syntrichia ruralis; Syntrichia caninervis |
| three-way genome-wide synteny comparisons with McScan |
inferred |
directionality of chromosomal rearrangement between Syntrichia species |
Syntrichia ruralis; Syntrichia caninervis; Ceratodon purpureus; Physcomitrella patens |
| CrusView |
is developed using |
SQLite databases |
|
| CrusView |
incorporates |
genomic karyotype information |
|
| af-flanking markers from the pea consensus genetic map and synteny relationships with close species |
used to mine |
candidate genes for Af |
Pisum sativum |
| synteny blocks on G. max chromosome 11 |
contains |
thirty-two genes |
Glycine max |
| Medtr5g014400 |
has conserved orthologues in |
G. max and A. thaliana |
Medicago truncatula; Glycine max; Arabidopsis thaliana |
| Arabidopsis thaliana |
used in comparison with |
fern species Ceratopteris richardii and Polypodium vulgare |
Arabidopsis thaliana; Ceratopteris richardii; Polypodium vulgare |
| limitation of de novo assembly |
makes difficult |
genomic macrosynteny analyses |
|
| CrusView |
is applicable to |
Brassicaceae species |
|
| CrusView |
performs visual comparison of |
Arabidopsis and E. salsugineum genomes |
Arabidopsis thaliana; Eutrema salsugineum |
| CrusView |
allows integration of |
self-defined genomic information |
|
| CrusView karyotype feature |
may facilitate understanding of |
karyotype evolution |
|
| CrusView karyotype feature |
may facilitate understanding of |
genome evolution |
|
| CrusView |
includes array of utilities to map |
list of genes of interest |
|
| chimeric assembly of the BAC contig or rearrangements between wheat and the other grass species in this region |
might suggest |
|
Triticum aestivum; Oryza sativa; Brachypodium distachyon |
| number of reads mapped to barley assembly |
decreased with |
phylogenetic distance |
Hordeum vulgare; Hordeum spontaneum; Hordeum bulbosum; Hordeum pubiflorum; Triticum aestivum |
| draft transcriptome |
shows |
high degree of conservation in comparative analysis versus other Brassicaceae species |
|
| comparative chromosome map of this region |
was constructed between |
cucumber and melon |
Cucumis sativus; Cucumis melo |
| 39 genes in Aegilops tauschii region |
most were |
non-syntenic genes only present in Aegilops tauschii |
Aegilops tauschii |
| this work |
describes |
analyses of two genome-wide datasets obtained for all diploid species of Aegilops, Amblyopyrum, and Triticum, and always multiple individuals per taxon |
Aegilops; Amblyopyrum; Triticum |
| 235 exclusive OGs in Ae. arabicum |
include |
1205 species-specific genes and 1268 genes not assigned to orthogroups |
Aethionema arabicum |
| other species-specific genes |
were annotated as |
cytochrome P450 (27), cysteine/histidine-rich C1 (32), domain of unknown function (DUF) (76), glycoside hydrolase (22), NAC domains (14), peptidases (40), protein kinases (15), WRKY (15), and zinc finger proteins (35) |
Aethionema arabicum |
| Aethionema arabicum |
has lower number of genes than |
other Brassicaceae |
Aethionema arabicum |
| CrusView |
may be used to perform |
karyotype-assisted genome synteny analysis |
|
| most analyses |
have focused on |
small number of plant genomes |
|
| barley and wheat orthologous gene sequences |
were used to compare |
discrete parts of Ae. markgrafii genome involved in rearrangements |
Aegilops markgrafii |
| orthologs |
detected with |
OrthoFinder (version 2.1.2) |
Arabidopsis thaliana; Capsella rubella; Glycine max; Zea mays; Oryza sativa; Solanum lycopersicum |
| PipMaker |
is used for |
identifying regions of homology between genomes |
|
| DiagHunter |
can operate on |
protein data |
|
| DiagHunter |
identifies synteny blocks despite |
high levels of background noise in comparisons |
|
| all chromosomes in one or more genomes |
can be run in |
batch process |
|
| draft genome sequence of chickpea and its analysis |
has provided |
rich information on similarity and diversity of structural and organizational components in relation to other sequenced legume genomes |
Cicer arietinum |
| orthologous genes in rice and Brachypodium |
are in |
same chromosomal regions |
Oryza sativa; Brachypodium distachyon |
| target regions from Morex assembly |
projected onto |
H. pubiflorum assembly |
Hordeum pubiflorum |
| Maximum-Likelihood phylogenetic trees |
were constructed with |
protein sequences predicted from M. polymorpha transcriptome assembly and published A. thaliana genome |
Marchantia polymorpha; Arabidopsis thaliana |
| DiagHunter |
can operate on |
nucleotide data |
|
| DiagHunter |
can carry out comparable predictions of segmental duplications in |
Arabidopsis |
Arabidopsis thaliana |
| COS markers |
provide access to |
robust links with sequence genomes and precise orthologous candidate genes |
Triticum aestivum |
| one-third of the N. tabacum (Hicks Broadleaf) WGP tags |
are not present or are undetectable in |
N. sylvestris or N. tomentosiformis |
Nicotiana tabacum; Nicotiana sylvestris; Nicotiana tomentosiformis |
| orthologous region of M. guttatus genome |
lies in |
484-kbp interval (2325–2809 kbp) on scaffold 4 |
Mimulus guttatus |
| 60S ribosomal protein gene |
was shared between |
Brachypodium and Aegilops tauschii |
Brachypodium; Aegilops tauschii |
| other grass genomes |
contain |
single copies of GLR gene |
Brachypodium; Oryza sativa; Sorghum bicolor |
| putative differentially fractionated genes |
were aligned to |
annotated genes present on scaffolds or contigs |
|
| synteny blocks between G. latifolia and G. max |
reproduced results from |
previous comparative analysis using shared SNP-containing sequences |
Glycine latifolia; Glycine max |
| assembly |
could still identify |
near complete synteny between (ATCAD7, CAD7, CHR, ELI3, ELI3-1, AT4G37980) 2 and 13 |
Linum usitatissimum |
| intragenomic, whole-genome analyses for synteny |
identified |
almost three times more syntenic relationships |
Spirodela polyrhiza |
| wild-type Cys residue |
is |
completely conserved across orthologous sequences |
Triticum aestivum; Triticum turgidum; Aegilops tauschii; Aegilops speltoides; Hordeum vulgare; Brachypodium distachyon; Oryza sativa; Zea mays |
| assembled translated pennycress transcriptome |
compared to |
peptide database from sequenced genomes |
Thlaspi arvense; Arabidopsis thaliana; Arabidopsis lyrata; Capsella rubella; Brassica rapa; Thellungiella halophila |
| limited overlaps of expressologs and enriched gene functions (ontologies) |
reflects |
lower similarity between endodermis/QC, vasculature, and meristematic cortex |
Arabidopsis thaliana; Solanum lycopersicum; Oryza sativa |
| Taxus wallichiana genes |
had one-to-one syntenic orthologs in |
Sequoiadendron giganteum |
Taxus wallichiana; Sequoiadendron giganteum |
| almost three times more syntenic relationships |
compared with |
similar analysis with previous Sp5909v3 assembly |
Spirodela polyrhiza |
| (PPR4, AT5G04810) and (EMB2654, AT2G41720) orthologs |
extracted from |
nuclear genome sequences from 14 phylogenetically diverse species |
|
| very small insertions and deletions |
do not correspond to |
sequences only found in A. lyrata |
Arabidopsis lyrata; Arabidopsis thaliana |
| T. salsuginea; L. virginicum; D. pinnata; T. parvula |
were selected for further analysis in comparison to |
Arabidopsis (glycophyte) and T. salsuginea (halophyte) |
Thellungiella salsuginea; Lepidium virginicum; Diplotaxis pinnata; Thellungiella parvula; Arabidopsis thaliana |
| research to elucidate function of rice genes |
would benefit greatly from |
direct integration and parallel comparison of information on orthologous genes in Arabidopsis |
Oryza sativa; Arabidopsis thaliana |
| plant families of microtubule-associated proteins (MAPs) |
examined through |
recently sequenced genomes |
Arabidopsis thaliana; Oryza sativa; Selaginella moellendorffii; Physcomitrella patens; Volvox carteri; Chlamydomonas reinhardtii |
| Cardamine hirsuta |
is |
experimental system for comparative studies |
Cardamine hirsuta; Arabidopsis thaliana |
| micro-synteny between Arabidopsis and B. rapa genomes |
exploited to identify |
candidate genes for QTL |
Arabidopsis thaliana; Brassica rapa |
| genome structure of Cardamine hirsuta with eight chromosomes and 24 conserved genomic blocks |
is similar to |
ACK and extant genomes of Arabidopsis lyrata and Capsella rubella |
Cardamine hirsuta; Arabidopsis lyrata; Capsella rubella |
| Syntrichia caninervis U and Syntrichia ruralis V sex chromosomes |
have significantly fewer syntenic blocks between |
homologous autosomes of these species |
Syntrichia ruralis; Syntrichia caninervis |
| study of wild relatives of Arabidopsis |
allows the use of |
molecular tools developed for Arabidopsis model |
Arabidopsis thaliana |
| 503 gene families |
were |
expanded in Amaranthus cruentus compared with the other 13 genomes |
Amaranthus cruentus |
| orthologous genes in rice and Brachypodium |
are separated by |
52 and 41 protein-coding genes in the two species, respectively |
Oryza sativa; Brachypodium distachyon |
| likelihood method implemented in cafe version 2.0 |
has been used in |
rhesus macaque genome |
Macaca mulatta |
| Cardamine hirsuta |
is |
genetic system for comparative studies |
Cardamine hirsuta |
| Arabidopsis AtGenExpress data |
were used following conversion of |
Arabidopsis genes into soybean orthologs |
Arabidopsis thaliana; Glycine max |
| 21 039 orthogroups |
<4% (773 orthogroups) are |
species-specific |
14 angiosperm species |
| Ancestral Crucifer Karyotype (ACK) |
defines |
24 conserved genomic blocks |
|
| sequencing technologies |
have driven |
mustard species into the spotlight of comparative research |
|
| gene01 and Os01g37800 and Bradi2g41180 |
share |
94 and 97% amino acid identities, respectively |
Triticum aestivum; Oryza sativa; Brachypodium distachyon |
| RT-directed Hidden Markov Model (HMM) |
serves to create |
cross-species profile of LINE RTs in plant genomes |
|
| 78.6% of Tnt1-flanking sequences |
matched |
coding sequence in Medicago truncatula |
Medicago truncatula |
| genes identified using multi-trait multi-SNP approach |
show |
syntenic conservation |
Zea mays |
| Qfs.zaas-6 |
was syntenic to |
cucumber fd5.2 |
|
| integration of species phylogeny |
enables exploration of |
functional relationships between omics data types |
|
| Collinearity of genes between the tetraploids and the reference genome DM |
was higher than |
that observed between the diploid (DAG1, AT3G61850) and RH |
Solanum tuberosum |
| DM |
was used as |
reference genome |
Solanum tuberosum |
| Collinear Blocks module table |
lists |
collinear blocks with detailed information |
|
| breakpoints of chromosomal translocation |
were determined by |
microcolinearity analysis of D. villosum and Ae. tauschii |
Dasypyrum villosum; Aegilops tauschii |
| synteny blocks on M. truncatula chromosome 5 |
contains |
fifty-two genes |
Medicago truncatula |
| 144 small ubiquitin-related modifier (SUMO) members |
identified in |
28 plant genomes |
|
| Nelumbo nucifera |
can be used as model for |
comparative and evolutionary genomics studies in angiosperms |
Nelumbo nucifera |
| uncertainty about whether ancestral functions have been partitioned between orthologues |
is a consequence of |
presence of multiple orthologues |
|
| PME and PMEI transcripts in garden cress CAP and RAD |
were compared with |
homologs in Arabidopsis |
Lepidium sativum; Arabidopsis thaliana |
| Darwin Tree of Life project |
allows examination of |
intra and interspecific centromere diversity |
|
| Zambian strain mini-chromosome |
was similar to |
B71 mini-chromosome |
Magnaporthe oryzae |
| 3891 collinear genes |
represent |
13.75% of 28 290 genes |
Acer truncatum |
| analysis of over 600 pennycress ESTs |
revealed |
close relationship between pennycress and Arabidopsis |
|
| M02_1500K marker ortholog |
maps to |
M. guttatus scaffold 89 at position 201 kbp |
Mimulus guttatus |
| 70 single-copy orthologous gene sets |
identified among |
25 genomes |
Chimonanthus praecox; Cassytha filiformis; Cinnamomum kanehirae; Persea americana; Litsea cubeba; Lindera benzoin; Sassafras albidum; Gomortega keule; Peumus boldus; Litsea chinense; Piper nigrum; Macleaya cordata; Vitis vinifera; Amborella trichopoda; Ginkgo biloba |
| PAV SPE genes |
showed average proportion categorized as |
syntenic (16%) |
Zea mays |
| eFP browser |
has been used for |
other species |
|
| comparative transcriptomics application in studying plant morphological diversity |
addresses challenges including |
identifying homologous gene pairs |
|
| large-scale comparative genomic approaches |
represent |
the only meaningful way of exploring the vast amount of available genomic data |
|
| Collinear Blocks module |
shows |
circle map with genes located in collinear blocks |
|
| 28 248 genes |
were unassigned to |
any cluster |
Solanum tuberosum |
| CPBD |
includes |
orthologous genes between 23 genomes |
|
| Gli-V2 on 6VS |
was collinear with |
homologous locus Gli-2 in CS |
Dasypyrum villosum; Triticum aestivum |
| locus on 4VL |
was specific to |
D. villosum |
Dasypyrum villosum |
| Plant T-2-T genomes |
ensure |
unified coordinate system for cross-comparison |
|
| genome-wide synteny analysis |
revealed |
evolutionary relationships among chromosomes |
Linum usitatissimum |
| 262882 genes |
assigned to |
23261 orthogroups |
Capsicum annum; Nicotiana benthamiana; Solanum chacoense; Solanum commersonii; Solanum lycopersicum; Solanum melongena; Solanum tuberosum |
| Plasmopara halstedii pathotype 710 genome assembly |
is significantly less fragmented and more syntenic to |
Plasmopara viticola genome assemblies |
Plasmopara halstedii; Plasmopara viticola |
| genomic regions in Thellungiella parvula contigs c2 and c3 |
matched |
distinct ancestral karyotype blocks |
Thellungiella parvula |
| lack of phylogenetic linkage between resurrection plants |
means that studies cannot be simply integrated |
comparative studies across resurrection plant species |
|
| Annotation of the A. cruentus assembly |
indicated |
gene number similar to A. hypochondriacus and closely related B. vulgaris |
Amaranthus cruentus; Amaranthus hypochondriacus; Beta vulgaris |
| multiple grass species |
can be employed as |
single genomic system |
|
| Plasmopara halstedii (CRN, SOL2, AT5G13290) effectors |
are conserved in |
at least 12 oomycete species |
Plasmopara halstedii |
| 4 core effectors (PhRXLR-C14, -C20, -C22 and -C29) |
having |
no homologs in the published Plasmopara halstedii sequence |
Plasmopara halstedii |
| pan-genome analyses |
uncovered |
32,986 distinct gene families |
Arabidopsis thaliana |
| Medicago truncatula and Glycine max |
were considered for |
candidate gene identification |
Pisum sativum; Medicago truncatula; Glycine max |
| reciprocal best hits (RBHs) from alignments between G. latifolia and G. max primary protein sequences |
were utilized as |
putative orthologous pairs for synteny block prediction |
Glycine latifolia; Glycine max |
| Camelina genes |
have homologs in |
Arabidopsis thaliana genes |
Camelina sativa; Arabidopsis thaliana |
| TaMs5 and TaMs1 |
have |
protein sequence similarity of less than 30% |
Triticum aestivum |
| putative (PPR4, AT5G04810) and (EMB2654, AT2G41720) binding sites |
extracted from |
respective chloroplast genomes |
|
| largest Thellungiella parvula contig c1 (13.08 Mb) |
aligned with |
entire length of one arm of Arabidopsis thaliana chromosome 1 |
Thellungiella parvula; Arabidopsis thaliana |
| contig c3 |
shared similarity with genes from |
three Arabidopsis thaliana chromosomes |
Thellungiella parvula; Arabidopsis thaliana |
| 3,118 predicted ORFs |
had no BLASTn hits to |
Arabidopsis thaliana cDNAs |
Thellungiella parvula; Arabidopsis thaliana |
| gene03 |
is orthologous and syntenic with |
rice chromosome 1 and Brachypodium chromosome 2 |
Triticum aestivum; Oryza sativa; Brachypodium distachyon |
| targets not covered in related species |
may not be captured or reads could not map due to |
excessive sequence divergence |
Hordeum pubiflorum |
| 'ZS11' genome |
identified |
35,337 gene pairs orthologous between An and Ar |
Brassica napus; Brassica rapa |
| 99 genes downregulated in both attdf1 and hvtdf1 |
included |
(AMS, AT2G16910) (ACOS5, AT1G62940) (FAR2, MS2, AT3G11980) (LAP5, PKSB, AT4G34850) /6, (AtMYB103, ATMYB80, MS188, MYB103, MYB80, AT5G56110) (KCS7, AT1G71160) /21, and (SHT, AT2G19070) |
Arabidopsis thaliana; Hordeum vulgare |
| TaMs5 |
is divergent to |
TaMs1 |
Triticum aestivum |
| putative differentially fractionated genes |
were aligned to |
expected syntenic position in opposite genotype |
|
| E169 and F242 in GhPGIP1 |
are |
corresponding residues from PvPGIP2 |
|
| annotation LiftOver procedures |
identified |
70, 256 and 219 genes with no hits in the other two assemblies for Lee, Wm82v4, and G. soja, respectively |
Glycine max; Glycine soja |
| Thellungiella parvula predicted ORFs |
primary matches to |
Arabidopsis thaliana coding regions (29%) |
Thellungiella parvula; Arabidopsis thaliana |
| comparative genomics analysis |
performed to uncover |
associations between key traits and gene families |
Cichorium intybus |
| pairwise comparison of Syntrichia ruralis and Syntrichia caninervis |
uncovered |
smaller inversion events along Syntrichia ruralis Chrs. 1, 2, 9, and 10 |
Syntrichia ruralis; Syntrichia caninervis |
| SynMap |
was used to identify |
blocks of syntenic genes |
|
| Kolukisaoglu and his co-workers |
identified |
10 OsCBLs and 30 OsCIPKs in rice |
Oryza sativa L. |
| orthologous groups containing genes involved in sesquiterpene synthase |
showed increased gene occupancy in |
tuber-bearing species |
Solanum chacoense; Solanum commersonii; Solanum tuberosum |
| orthology analysis |
revealed |
core set of 158367 Solanaceae genes |
Capsicum annum; Nicotiana benthamiana; Solanum chacoense; Solanum commersonii; Solanum lycopersicum; Solanum melongena; Solanum tuberosum |
| (MS5, TDM1, AT4G20900) and (MS1, AT5G22260) |
are |
distinct to other members of wheat (LTP, LTP7, AT2G15050) super-family |
Triticum aestivum |
| assembled sequences surrounding the GPA-resistant locus |
were compared between |
(HAP1, MAGO, MEE63, AT1G02140) and (GCS1, HAP2, AT4G11720) genomes |
Prunus persica |
| Wang et al. |
computationally compared |
derived protein clusters with established gene families in budding yeast |
Arabidopsis thaliana; Saccharomyces cerevisiae |
| the COGs |
have been used for |
genome-wide evolutionary studies |
|
| REPuter |
is used for |
identifying regions of homology between genomes |
|
| BLAST alignments |
used to validate and identify |
missed syntenic assignments |
|
| G. latifolia pseudomolecule 2 |
contained |
10-Mb region colinear with syntenic G. max chromosome 19 |
Glycine latifolia; Glycine max |
| Saccharomyces cerevisiae |
has |
very small genome (~12.2 Mbp/1C) |
Saccharomyces cerevisiae |
| Ms5-A |
shows |
76.5% amino acid identity with B. distachyon |
Triticum aestivum; Brachypodium distachyon |
| differences in gene numbers |
may arise from |
greater completeness of Wm82v4 assembly or true gene presence/absence variation |
Glycine max; Glycine soja |
| introns |
behave similarly |
intergenic regions |
Arabidopsis lyrata; Arabidopsis thaliana |
| raw SynMap analysis |
identified |
20,446 genes in PH207 with syntenic orthologs in sorghum |
|
| syntenic identification software |
has limitations that may underestimate |
number of syntenic genes identified |
|
| genes with high protein sequence similarities |
indicative of |
close/similar biological functions |
|
| ortholog clustering analysis using protein sequences |
identified |
9700 gene families among selected dicotyledonous plant species |
Glycine latifolia; Glycine max; Arabidopsis thaliana; Populus trichocarpa; Vitis vinifera |