| MYB, WD40, (bHLH, AT5G51780) NAC, WRKY, and (AtbZIP, bZIP, AT1G68880) |
may play important roles |
in regulatory network |
Quercus dentata |
| HvAMS expression pattern in barley |
indicates AMS is also regulated by |
other currently unknown transcription factors |
Hordeum vulgare |
| expression line |
enables |
tissue-specific gene expression of the reporter and the effector |
Arabidopsis thaliana |
| three deletions and five SNP sites in lncRNA1 promoter |
caused |
higher expression level of LncRNA1 in 'Zhaoshouhong' |
Prunus persica |
| alternative splicing |
is involved in |
regulatory processes |
|
| 48 important TFs |
identified from |
brown-coded co-expression module |
Quercus dentata |
| expression of SE (AtDRB1, DRB1, HYL1, AT1G09700) and (ASU1, ATDCL1, CAF, DCL1, EMB60, EMB76, SIN1, SUS1, AT1G01040) |
could be under either direct or indirect control of |
(BZR1, AT1G75080) |
Arabidopsis thaliana |
| (ATMYB35, MYB35, TDF1, AT3G28470) and (AMS, AT2G16910) co-expressed |
suggests important role of |
TDF1–AMS complex in regulating (AtMYB103, ATMYB80, MS188, MYB103, MYB80, AT5G56110) expression |
Arabidopsis thaliana |
| cognate promoter consisting of six 52 bp lac operator (Op6) copies |
enables |
tunable expression of downstream gene based on inducer concentration |
Arabidopsis thaliana |
| (H3.3, HTR8, AT5G10980) |
was enriched in |
actively transcribed genes |
Arabidopsis thaliana |
| Sph/RY motif |
is enriched in |
promoter and intron regions of LAFL genes |
|
| MYB family members |
most members (11) belonged to |
subnetwork of (ANS, LDOX, TDS4, TT18, AT4G22880) and (ATCHS, CHS, TT4, AT5G13930) |
Quercus dentata |
| (AGO7, ZIP, AT1G69440) knockdown |
destabilizes/disrupts |
regulatory networks and reverses outcomes of several miRNA-mRNA interactions |
Nicotiana attenuata |
| sugar-responsive genes |
includes |
transcription factors |
Arabidopsis thaliana |
| host-specific infection strategy |
is mediated through |
transcription-based control of essential effector genes |
Colletotrichum orbiculare |
| FTSZ1-11 line |
shows significant reduction in |
native (ATFTSZ1-1, CPFTSZ, FtsZ1, FTSZ1-1, AT5G55280) gene expression |
Nicotiana tabacum |
| MpGLK |
functions as |
transcriptional activator of the Mp (AtMAX2, MAX2, ORE9, PPS, AT2G42620) gene |
Marchantia polymorpha |
| transcription factors |
are highlighted as |
gene expression and epigenetics modulators |
Populus trichocarpa |
| SE and (AtDRB1, DRB1, HYL1, AT1G09700) |
are identified in |
list of (BZR1, AT1G75080) target genes |
Arabidopsis thaliana |
| Ib (bHLH, AT5G51780) transcription factors |
regulate |
(HTB4, AT5G59910) expression |
Arabidopsis thaliana |
| noncoding RNAs (ncRNAs) |
play important roles in regulating |
gene expression |
|
| gene network between (ATMYB35, MYB35, TDF1, AT3G28470) and (AMS, AT2G16910) |
is not as simple as |
inclusion relationship |
Hordeum vulgare; Arabidopsis thaliana |
| ACGT-containing element cis-element |
is located in |
downstream promoters of EARLY FLOWERING 4 and (FHY1, FRY1, PAT3, AT2G37678) HOMOLOG |
|
| FBS motif cis-element and ACGT-containing element cis-element in downstream promoters of EARLY FLOWERING 4 and (FHY1, FRY1, PAT3, AT2G37678) HOMOLOG |
are close to each other (less than 20 bp away) |
|
|
| QdMYB QD01G020890 gene product |
could bind to |
cis elements in promoter region of gene QdCHS QD06G044950 |
Quercus dentata |
| transgenic plants expressing full-length WT ( (PAP3, PIF3, POC1, AT1G09530) WT), nonphosphorylatable ( 6A) and phospho-mimicking ( 6D) |
were under control of |
native (PAP3, PIF3, POC1, AT1G09530) promoter |
Arabidopsis thaliana |
| chromatin structure |
is key in |
regulation of gene expression |
|
| whole-genome duplications (WGDs) |
can increase |
expression of genes that underpin critical traits |
|
| expression levels of MpPIN2, MpKAI2A, MpKAI2B, MpMAX2, and MpCPS |
were not significantly different in |
MpPUB9-overexpressors |
Marchantia polymorpha |
| trans-acting effects of climate-associated DMRs |
on |
environmentally responsive genes |
Fragaria vesca |
| effector genes |
are specifically overexpressed upon |
KMT1 silencing |
Leptosphaeria maculans |
| pleiotropic effects of a flowering time regulator (FLA, FRI, RSB7, AT4G00650) |
affects |
expression of (AGL25, FLC, FLF, RSB6, AT5G10140) |
Arabidopsis thaliana |
| higher methylation variation and number of gene- and TE-related DMRs in the field |
suggest a potential association between |
natural environmental conditions and regulation of gene expression |
Fragaria vesca |
| (ATPDX1.1, PDX1.1, AT2G38230) |
expression is induced by |
indole acetic acid (IAA) |
Arabidopsis thaliana |
| edges with r ≤ −0.9 in biotic stresses |
are more abundant than |
edges with r ≤ −0.9 in abiotic stresses |
Oryza sativa |
| laser-captured tissue sections or cells sorted by fluorescent marker expression |
enables refinement of knowledge of |
gene activity at cell-type-specific and single-cell level |
|
| OsmiR396d |
has |
12 putative targets |
Oryza sativa |
| ectopic expression of AtTDF1 regulated by (DYT1, AT4G21330) promoter |
confirms need for |
precise spatial and temporal expression of (ATMYB35, MYB35, TDF1, AT3G28470) gene |
Arabidopsis thaliana |
| yeast two-hybrid (Y2H) assays |
performed to verify |
regulatory relationships among key TFs and structural genes |
Quercus dentata |
| SlTCP24/29 and CLAUSA |
may have |
feedback regulation |
Solanum lycopersicum |
| inducible overexpression of (bHLH, AT5G51780) transcription factors |
enhances |
(HTB4, AT5G59910) expression |
Arabidopsis thaliana |
| (HTB4, AT5G59910) transcription |
is regulated by |
age and Fe deficiency |
Arabidopsis thaliana |
| presence of (H2A.Z, HTA11, AT3G54560) in gene bodies |
is associated with |
transcriptional repression |
|
| (SPL3, AT2G33810) |
was strongly up-regulated in |
irAGO7 during the early stages of colonization |
Nicotiana attenuata |
| SUSIBA1 and SUSIBA2 |
is |
members of plant-specific WRKY family |
|
| GtMYB3 |
activates |
F3′5′H promoter |
Gentiana triflora |
| (AMS, AT2G16910) expression in barley |
suggests some other transcription factors may also take part in regulating |
(AMS, AT2G16910) expression |
Hordeum vulgare |
| (ATCHS, CHS, TT4, AT5G13930) and (ANS, LDOX, TDS4, TT18, AT4G22880) gene promoter regions |
both carry |
MYB binding sites |
Quercus dentata |
| DNA methylation |
influences |
gene expression |
|
| different sets of effector proteins |
are regulated via |
transcriptional regulation |
Colletotrichum orbiculare |
| HvTDF1 |
might be involved in regulating |
biological processes affected in hvtdf1 mutant |
Hordeum vulgare |
| (AtMYB103, ATMYB80, MS188, MYB103, MYB80, AT5G56110) |
is downstream of |
(AMS, AT2G16910) |
Arabidopsis thaliana |
| (AMS, AT2G16910) or (ATMYB35, MYB35, TDF1, AT3G28470) |
can bind to MYB80 promoter and activate expression |
(AtMYB103, ATMYB80, MS188, MYB103, MYB80, AT5G56110) |
Arabidopsis thaliana |
| promoter methylation |
may have positive effects on |
expression |
|
| 198 related TFs (transcription factors) |
examined for |
brown-coded module |
Quercus dentata |
| nuclear sphingolipids |
can modulate |
expression of genes involved in various physiological processes |
Arabidopsis thaliana |
| novel screening assays |
could support identification of |
genetic mechanisms controlling dynamic responses to fluctuating environmental conditions |
|
| reduced DNA methylation levels |
may release |
transcriptional repression of associated genes |
Phyllostachys edulis |
| genes with no polymorphisms |
might be expressed differently as |
indirect effect of mutation in a trans-acting factor elsewhere in the genome |
Zea mays |
| repeat Ser insertions |
can enhance |
transcriptional regulatory activity |
Malus domestica |
| changes in chromatin structure |
were recently linked to |
regulation of GA 2-oxidase gene in Arabidopsis root meristems |
Arabidopsis thaliana |
| (chr13, PIE1, SRCAP, AT3G12810) inactivation |
results in misregulation of |
627 to 938 genes |
Arabidopsis thaliana |
| deletion of ftsZ1-2 gene |
did not affect |
(ATFTSZ1-1, CPFTSZ, FtsZ1, FTSZ1-1, AT5G55280) transcript abundance |
Physcomitrella patens |
| (AtbZIP, bZIP, AT1G68880) WRKY, and NAC |
may participate as |
secondary regulators |
Quercus dentata |
| induced endogenous HSC70.4 expression |
was detected in |
hsc70.1 mutant |
Arabidopsis thaliana |
| reduced expression of ZmTFCB in the (ASG6, CRK2, AT1G70520) mutant |
was most likely caused by |
unbalanced cis-trans regulation of ZmTFCB when one line with more copies introgressed into single copy line |
Zea mays |
| silencing of KMT1 |
leads to |
overexpression of > 30% of genes located in TE-rich environments |
Leptosphaeria maculans |
| combining single-cell RNA-Seq and single-cell proteomics data |
could gain insight of |
genetic regulation of protein content at the single-cell level |
|
| Sph/RY motifs |
are consistent with direct regulation by |
B3 transcription factors |
|
| miR473 overexpression |
reduced colonization by significantly reducing |
ALKK, (PAP12, PDE225, PTAC7, TAC7, AT5G24314) and GAI1-DELLA transcript levels |
|
| GO term analysis of downregulated genes from hvtdf1 mutant |
shows several key biological processes have been affected in |
hvtdf1 mutant |
Hordeum vulgare |
| variant spliceosomes |
contribute to |
gene regulation in tissue/cell-specific manner |
|
| chromatin condensation state |
directly impacts |
gene expression |
|
| methylation of gene promoters |
regulates |
gene expression |
|
| heritable epigenetic variation |
has |
functional role |
Fragaria vesca |
| regulation during root oxygen loss barrier formation |
differs between |
apical and basal parts of roots |
|
| small RNAs |
are recognized as |
key genetic and epigenetic regulators of development |
|
| specific gene regulatory networks |
operate through |
both genetic and epigenetic signals |
Phyllostachys edulis |
| Three osmotin protein family genes |
had a similar RNA expression pattern as |
HvTDF1 |
Hordeum vulgare |
| yeast one-hybrid (Y1H) assays |
performed to verify |
regulatory relationships among key TFs and structural genes |
Quercus dentata |
| feedback regulation in the CLAUSA pathway |
may regulate |
SlTCP29 |
Solanum lycopersicum |
| (AMS, AT2G16910) ortholog gene |
is downregulated in |
hvtdf1 mutant |
Hordeum vulgare |
| (ATMYB35, MYB35, TDF1, AT3G28470) and (AMS, AT2G16910) |
are unable to work alone in regulating |
(AtMYB103, ATMYB80, MS188, MYB103, MYB80, AT5G56110) |
Arabidopsis thaliana; Hordeum vulgare |
| reporter gene mTurquoise2 |
is controlled by |
pOp6 promoter |
Arabidopsis thaliana |
| transcription of (SLG1, AT5G08490) and PSY3 isoforms |
is |
coordinated |
Solanum lycopersicum |
| transgene expression |
causes slight reduction in |
native gene expression |
Nicotiana tabacum |
| miR473 |
targets genes related to |
GA signaling and fatty acid metabolism |
|
| Cf-9B resistance pathway activation in young plants |
is in line with |
Cf-9B expression not being developmentally regulated |
Solanum lycopersicum |
| OPM1 and OPM2 expression |
is regulated by |
unknown regulatory mechanisms |
Hordeum vulgare |
| expression of ZmTFCB |
is significantly negatively associated with |
CNVs |
Zea mays |
| transcription factors (TFs) |
regulate |
nuclear gene expression |
|
| many transposons |
can serve as |
promoters or enhancers |
Zea mays |
| transcript levels of RAP2-7, (AP2, AtAP2, FL1, FLO2, AT4G36920) (APL, WDY, AT1G79430) and (AtPED2, ATPEX14, PED2, PEX14, AT5G62810) |
were low in |
irAGO7 plants |
Nicotiana attenuata |
| copy-neutral structural variants |
can affect gene expression by |
changing regulatory elements or creating positional effects |
|
| KN1 target (ATGA2OX1, GA2OX1, AT1G78440) |
was up-regulated in |
leaves of dominant knox mutants Gn1-R and Lg3-O |
Zea mays |
| (AtPIF4, PIF4, SRL2, AT2G43010) expression |
is up-regulated in |
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutant in presence of sucrose |
Arabidopsis thaliana |
| LOC_Os03g57200 |
has |
93 high-correlation edges |
Oryza sativa |
| LOC_Os01g13570 |
has positive edge to |
SOUL heme-binding protein |
Oryza sativa |
| expression of photosynthetic genes |
was suppressed in |
P– (inorganic phosphate-deficient) roots |
|
| two subnetworks |
inferred for |
brown-coded module with TFs as potential regulators |
Quercus dentata |
| epigenetics |
is defined as |
process affecting gene expression without a change in the DNA sequence |
|
| co-expression network analyses |
revealed |
specific modules with strong correlation with genotype in all three root zones |
Hordeum vulgare |
| histone variants |
play crucial roles in |
gene expression |
|
| gene regulation hypothesis |
suggests that |
regulatory loci may exert environmentally dependent phenotypes |
|
| mobilization of transposons driven by stress |
may reconfigure |
gene regulatory network by inserting close to key relevant genes |
Phyllostachys edulis |
| (ATGA2OX1, GA2OX1, AT1G78440) |
was up-regulated in |
Lg3 and (AtSIP1, RS1, SIP1, AT1G55740) dominant mutants |
Zea mays |
| (ATPDX1.1, PDX1.1, AT2G38230) and (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) |
are regulated differently |
gene expression |
Arabidopsis thaliana |
| expression of 214 transcription factors in (AQC1, HPS7, TPST, AT1G08030) roots |
was altered relative to |
wild type |
Arabidopsis thaliana |
| elaborately branched networks of regulons |
are induced by |
stimulus |
|
| unidentified Guy11 effector(s) |
may bind directly or indirectly to |
cis-elements |
Oryza sativa; Magnaporthe oryzae |
| elimination of introns |
could potentially release |
translational regulation |
Oryza sativa |
| class B-Hsfs |
may act as |
repressors of target gene expression |
|
| transcript expression of a pair of Golgi-localized putative pectinmethyltransferases |
is strongly correlated with |
(GAUT1, LGT1, AT3G61130) expression |
|
| (ATCHS, CHS, TT4, AT5G13930) and (ANS, LDOX, TDS4, TT18, AT4G22880) genes |
are hubs within |
potential regulatory relationships |
Quercus dentata |
| F3′5′H promoter |
induces |
petal-specific expression |
Gentiana triflora |
| SG19 MYB-binding site in EOB1 promoter |
is located |
450 bp before START codon of EOB1 |
Petunia axillaris |
| LTR regions functioning as promoters, enhancers, or destroyers |
govern |
expression of neighboring genes |
|
| silencing of (PAT24, TIP1, AT5G20350) ;1 |
would not influence |
transcript levels of genes upstream in the gene hierarchy |
Solanum lycopersicum |
| promoters of OLEIC ACID-REQUIRING1 (OLE1) and (AAD6, FTM1, HUP7, SAD6, AT1G43800) genes |
share |
low-oxygen-responsive cis-activation elements |
|
| sparse cluster of negative edges |
is shown in |
coexpression network visualization |
Oryza sativa |
| (ERF017, ERF17, AT1G19210) allele |
reveals |
a regulatory mechanism associated with its natural variation |
Malus domestica |
| lincRNAs found a short distance from protein-coding genes |
could modulate expression of their neighbors by actively recruiting |
activators, repressors, and epigenetic modifiers |
Glycine max |
| GFP reporter gene |
was fused to |
wild-type or deletion mutants of (MIR319, MIR319B, AT5G41663) promoter |
Oryza sativa |
| TC-rich repeats and Box-W1 motif |
do not function redundantly in |
(MIR319, MIR319B, AT5G41663) promoter regulation |
Oryza sativa |
| 14 transcription factors with significant edges |
include |
Nuclear Factor Y, G2-like, and (bHLH, AT5G51780) TF families |
Oryza sativa |
| GROWTH REGULATING FACTOR 6 (14-3-3lambda, AFT1, GRF6, AT5G10450) |
is |
one of OsmiR396d targets |
Oryza sativa |
| abscisic acid (ABA) |
has selective inhibitory effect on |
gene expression in embryo axis |
Medicago truncatula |
| 93 unique transcripts |
are regulated by RTCS |
constitutively |
Zea mays |
| SNPs and INDELs in differentially expressed genes |
discriminate from |
indirect effects of trans-acting factors in genome |
Zea mays |
| regulatory components found in plants such as Arabidopsis and rice |
have been attenuated or lost |
in Hakea prostrata |
Hakea prostrata |
| microRNA (miRNA) |
play pivotal roles in |
various biological processes |
|
| Lsi1 expression |
was not affected by |
external boron level |
Oryza sativa |
| introns |
may be recruited in |
post-transcriptional control |
Oryza sativa |
| metabolism |
is regulated |
transcriptional control |
|
| miR156 |
is |
microRNA |
|
| (AtBOR1, BOR1, AT2G47160) |
is regulated at |
posttranscriptional regulation in response to external boron change |
Arabidopsis thaliana |
| OsBOR1 protein |
seems to be enhanced |
at protein level |
Oryza sativa |
| RH50 |
is coregulated with |
(GUN1, AT2G31400) |
Arabidopsis thaliana |
| OsMADS8 RNAi line |
shows increased expression of |
OsTGA10 |
Oryza sativa |
| candidate functional SNPs |
may be from |
microRNAs and microRNA-target complementary sites |
|
| high tissue-specific lincRNA expression |
supports |
idea of their highly specialized, possible regulatory functions |
Glycine max |
| (MIR319, MIR319B, AT5G41663) promoter region |
contains |
hormone-responding elements |
Oryza sativa |
| signaling pathways |
may finally lead to |
alterations in gene expression |
|
| posttranscriptional regulation of lipid metabolism |
perhaps through |
selective RNA translation and protein turnover |
|
| NUCLEAR FACTOR Y (NF-Y) transcription factors |
has |
79 significant edges |
Oryza sativa |
| protein absence |
was not a |
regulatory effect |
Zea mays |
| (GF14 UPSILON, GRF5, AT5G16050) mRNAs |
are not targeted by |
miR396 |
Arabidopsis thaliana |
| (GF14 UPSILON, GRF5, AT5G16050) 35S:MIR396b plant |
should further reduce |
levels of total GRF mRNAs |
Arabidopsis thaliana |
| expression levels of the other four MdBT genes |
changed |
MdBT gene expression |
|
| hydroxycinnamoyl CoA:shikimate/quinate hydroxycinnamoyltransferase (HCT, AT5G48930) |
may require regulation at |
multiple levels |
|
| HAT and HDAC proteins |
are associated with |
actively transcribed genes |
|
| constitutive overexpression of Maize (ABI3, AtABI3, SIS10, AT3G24650) lacking B3 domain |
results in upregulation of |
subset of ABI3-regulated genes |
Zea mays |
| phS:yfp gene in transformants |
is |
sex inducible |
Volvox carteri |
| OsCKX4 promoter |
contains |
one auxin response element |
Oryza sativa |
| microRNAs (miRNAs) |
regulate and fine-tune |
gene expression |
|
| wild-type or mutant promoter |
was expressed at similar level under |
mock-treated condition |
Oryza sativa |
| LeHT1 |
is preferentially expressed in |
resistant (R) plants |
Solanum lycopersicum |
| light quantity and light quality signals |
should show at least partial convergence in |
control of target genes |
Arabidopsis thaliana |
| genetic studies |
have shown that |
transcriptional control is very important to phenotype manifestation |
|
| phytochromes |
do not effect gene regulation via |
direct DNA binding |
Arabidopsis thaliana |
| increased Pseudomonas syringae pv. maculicola ES4326-induced pectin methylesterase (PME) activity in (ATPME3, OZS2, PME3, AT3G14310) and (PME12, AT2G26440) mutants |
possibly due to |
overcompensation for loss of these (PMES, AT4G10050) |
Arabidopsis thaliana |
| down-regulation of the transcript levels of several known CAM-associated genes |
is |
specific effect that could be the result of metabolic feedback regulation of gene expression and/or transcript stability |
Kalanchoë fedtschenkoi |
| chromatin structure changes by histone modification |
can change |
target gene expression |
|
| EMBRYONIC FLOWER1 (EMF1, AT5G11530) |
binds |
DNA |
Arabidopsis thaliana |
| coexpression analysis of Arabidopsis under several types of biotic stress at early stages of infection |
revealed |
positive correlation between TIP-AQP, hexose transport, and hormone pathways |
Arabidopsis thaliana |
| impairment in (EAL1, SGR7, SHR, AT4G37650) expression levels in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) |
is consequence of |
mutation in (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) |
Arabidopsis thaliana |
| gene expression |
is regulated epigenetically |
epigenetic regulation |
|
| (AOX1D, AT1G32350) |
may be subject to |
redox or metabolic regulation at translational and post-translational levels |
|
| PXR receptor |
controls expression of |
CYP450 genes |
|
| large insertion into promoter of S. lycopersicum CXE1 |
resulted in |
much higher expression of SlCXE1 |
Solanum lycopersicum; Solanum pennellii |
| partial AuxRE (TGTCTc) |
is located in |
promoter region of (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) |
Arabidopsis thaliana |
| parallels observed between lincRNA and transcription factor expression |
can suggest |
similar roles of lincRNAs |
Glycine max |
| gene expression |
is tightly regulated |
gene regulation |
|
| heritable epigenetic changes in gene expression |
includes |
accumulation of miRNAs in sperm |
Mus musculus |
| unique pattern of (PAT24, TIP1, AT5G20350) ;1 expression correlation |
was not observed for |
other TIP genes |
Arabidopsis thaliana |
| flv4-2 operon expression |
is tightly regulated by |
CO2 levels |
Synechocystis sp. PCC 6803 |
| Z1C genes identified here |
are also likely |
O2 independent |
Zea mays |
| enhanced expression of stem cell transcription factor PLTs |
is hypothesized to affect |
expression of a large number of transcription factors |
Arabidopsis thaliana |
| expression pattern of (AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) |
is important for |
predominant biological roles of (AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) |
Arabidopsis thaliana |
| candidate functional SNPs |
may be from |
protein-DNA binding sites |
|
| identical predicted ORFs of GA2oxA9 between mutants and wild types |
indicates that changes in gene expression most probably were responsible for |
mutant phenotype |
|
| SA-responsive element (TCA element) |
was identified in |
(MIR319, MIR319B, AT5G41663) promoter |
Oryza sativa |
| Minor QTL genes in pyramiding strategy |
have expression that can be |
managed |
Oryza sativa |
| in cis interactions |
is mechanism involved in |
gene regulation |
|
| (MFP1, AT3G16000) (MAR BINDING FILAMENT-LIKE PROTEIN 1) |
is |
chloroplast phosphoprotein |
Arabidopsis thaliana |
| yabby15 |
was up-regulated in |
Lg3 and (AtSIP1, RS1, SIP1, AT1G55740) dominant mutants |
Zea mays |
| sequence TAACAAA |
is located immediately upstream of |
(ATPDX1.1, PDX1.1, AT2G38230) |
Arabidopsis thaliana |
| LOC_Os11g26780 |
had |
one significant positive edge with another dehydrin gene |
Oryza sativa |
| RPL27aC expression levels in the ovule |
regulate |
expression of one or both (RPL27A, RPL27AB, uL15y, AT1G23290) paralogs |
Arabidopsis thaliana |
| (PXY, TDR, AT5G61480) |
regulates |
(ACO4, EAT1, EFE, AT1G05010) transcription |
Oryza sativa |
| long noncoding RNAs (lncRNAs) |
are involved in |
homeobox gene expression |
|
| endosperm-expressed C1 genes |
not up-regulated in |
FIS-PRC2 mutants |
|
| unique pattern of (PAT24, TIP1, AT5G20350) ;1 expression correlation |
was not observed for |
other STP genes |
Arabidopsis thaliana |
| step-wise silencing and gene transcript level analyses |
indicated that |
Lin6 is upstream of LeHT1 |
Solanum lycopersicum |
| (ATPDX1.1, PDX1.1, AT2G38230) expression |
is repressed by |
sucrose |
Arabidopsis thaliana |
| coexpression patterns |
is hallmark of |
coordinated expression regulation mediated by presence of particular motif or motif combination |
|
| gene expression |
plays a role in |
regulation of cellular mechanisms influencing developmental and salt-induced ploidy levels |
Mesembryanthemum crystallinum |
| kinetic patterns |
can be correlated with |
gene function |
|
| PIN proteins |
exhibit synergistic interactions in |
pin mutants |
Arabidopsis thaliana |
| (ATPIN3, PIN3, AT1G70940) expression |
is down-regulated in |
root tips |
Arabidopsis thaliana |
| signaling pathways |
lead to |
changes in gene expression |
|
| mutation of the (AQC1, HPS7, TPST, AT1G08030) gene |
caused |
many transcription factors to be up-regulated or down-regulated |
Arabidopsis thaliana |
| ORR2 and ORR3 |
induce |
β-galactosidase (LacZ) reporter gene expression driven by OsCKX4 promoter |
Oryza sativa |
| dexamethasone-inducible promoter |
controls expression of |
transcription factor couple from Antirrhinum |
Solanum lycopersicum |
| OsmiR396d |
controls yield traits through |
different downstream targets |
Oryza sativa |
| transcriptional network motifs |
are shared between |
eukaryotes and non-chromatin organisms such as bacteria |
|
| deletion of any of the (ATFTSZ1-1, CPFTSZ, FtsZ1, FTSZ1-1, AT5G55280) genes |
most affected |
transcript abundances of (ATFTSZ2-1, FTSZ2-1, AT2G36250) |
Physcomitrella patens |
| deletion of the (ATFTSZ1-1, CPFTSZ, FtsZ1, FTSZ1-1, AT5G55280) genes |
led to reduced transcript levels of |
(ATFTSZ2-1, FTSZ2-1, AT2G36250) |
Physcomitrella patens |
| chosen promoters |
lacked |
specificity |
|
| miR1317 |
was predicted to target |
transposon protein gene (LOC_Os10g20480) |
Oryza sativa |
| interference with YHB:YHB homodimer activity |
effects |
suppression of gene expression |
|
| sole presence of histone marks such as H3K27me3 |
does not allow conclusion that target gene relies on epigenetic mechanisms for |
bistable regulation |
|
| tail-to-tail gene orientation |
intergenic space does not contain |
promoter |
Arabidopsis thaliana |
| methanol (MeOH) |
down-regulates expression of |
pathogen-related GhPMEI3 |
Gossypium hirsutum |
| (AGL25, FLC, FLF, RSB6, AT5G10140) (AGL9, SEP3, AT1G24260) and AG genes |
were hardly regulated by |
NF-YC |
|
| (AGL91, AT3G66656) |
not repressed by |
FIS-PRC2 |
|
| deacetylation |
is associated with |
transcriptional suppression |
|
| MtMYB5 |
regulates a broader set of genes than |
MtMYB14 |
Medicago truncatula |
| negative edges in biotic stresses |
are more abundant than |
negative edges in abiotic stresses |
Oryza sativa |
| genes harboring the same upstream motif |
may have similar |
function |
Arabidopsis thaliana |
| C2 genes |
constitute majority of |
type I MADS-box genes up-regulated or down-regulated in paternal-excess or maternal-excess crosses |
|
| PIN proteins |
exhibit synergistic interactions |
cross-regulation of PIN gene expression |
Arabidopsis thaliana |
| small non-coding RNAs (sRNAs) |
play essential roles in regulating |
molecular machinery of eukaryotic cells |
|
| (CLPR4, HON5, AT4G17040) (HIGH MOBILITY GROUP FAMILY A 5) |
is |
chloroplast phosphoprotein |
Arabidopsis thaliana |
| moderate transcriptional response in Hakea prostrata |
shows |
this species has not entirely lost capacity to regulate phosphorus (P) use for lipid metabolism through changes in gene expression |
Hakea prostrata |
| 208 genes in positive edges |
include |
194 (93%) genes with conserved down-regulation |
Oryza sativa |
| α-zeins |
may be repressed through |
unknown feedback mechanism resulting from reduced γ-zein synthesis |
Zea mays |
| MeJA-responsive element (CGTCA motif) |
was identified in |
(MIR319, MIR319B, AT5G41663) promoter |
Oryza sativa |
| expression pattern of Class I KNOX genes |
determines |
function of Class I KNOX genes |
Arabidopsis thaliana |
| redox |
has emerging regulatory roles in |
transcription |
|
| methylation of histone H3 lysine 4 (H3K4) |
correlates with |
transcriptional stimulation |
|
| fine tuning of gene expression |
is achieved by |
sophisticated mechanisms |
|
| nuclear roles of npcRNAs |
can have consequences on |
generation of novel patterns of gene expression |
|
| NblA expression |
is adjusted by |
response regulator NblR |
cyanobacteria |
| MYB transcription factors |
are overrepresented with |
14 genes out of 43 |
Petunia axillaris; Petunia exserta; Petunia parodii |
| DNA methylation |
can result in changes at |
biochemical, genetic and epigenetic levels |
|
| decrease in H3K27me3 levels at (MIR156A, AT2G25095) /C loci |
leads to |
upregulation of gene expression at (MIR156A, AT2G25095) /C loci |
Arabidopsis thaliana |
| histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) |
is positive regulator of |
gene expression of protein tyrosine phosphatases |
Arabidopsis thaliana |
| absence of orthologs in Hakea prostrata transcriptome database |
for many lipid genes that are induced by |
myeloblastosis transcription factor PHOSPHATE STARVATION RESPONSE1 (AtPHR1, PHR1, AT4G28610) in response to phosphorus (P) limitation in Arabidopsis |
Hakea prostrata; Arabidopsis thaliana |
| cis-regulatory motifs |
are located in |
gene promoter regions |
Arabidopsis thaliana |
| MdERF3 |
binds to |
its promoter |
Malus domestica |
| reduction of YHB protein abundance |
could be responsible for |
global suppression of YHB transcriptome |
|
| (ARF16, AT4G30080) |
is predicted to repress |
transcription |
|
| (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) and (NDB2, AT4G05020) |
have similar CAREs in |
promoters |
Arabidopsis thaliana |
| QdMYB QD01G020890 and QdNAC QD08G038820 |
identified as |
important upstream regulators |
Quercus dentata |
| Cnr mutation |
is |
epigenetic change |
|
| (CCR2, CRTISO, AT1G06820) promoter |
shows atypical reporter gene expression potentially due to |
chromosomal position effects |
Arabidopsis thaliana |
| histone lysine methylation |
plays important role in |
reprogramming of gene expression |
|
| ccc mutant |
shows no change in expression of |
(ATCAD4, CAD, CAD-C, CAD4, AT3G19450) G gene |
Arabidopsis thaliana |
| photosynthetically active light without photosynthetic inhibitors |
allows testing |
role of plastoquinone (PQ) pool in state transitions, gene regulation and acclimation reactions |
|
| hindrance of demethylation during ripening |
may affect |
acs2-2 transcript levels |
Solanum lycopersicum |
| deletion of the psbA2 gene copy |
is fully compensated by |
expression of the psbA3 gene |
Synechocystis |
| 3,701 shared edges |
connect |
381 genes |
Oryza sativa |
| changes in expression levels of other four MdBT genes |
possibly due to |
functional redundancy and mutual regulation among the MdBT genes |
|
| in trans regulation |
is important in |
higher eukaryotes |
|
| genes enriched for H3K27me3 |
frequently exhibit |
tissue-specific expression |
Arabidopsis thaliana |
| epigenetic mechanisms |
may be basis of |
response hysteresis |
|
| suppression of LHPI, (CMT3, AT1G69770) (ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) and (ATSUVH2, SDG3, SUVH2, AT2G33290) in CCT431 |
may have indirect effects through |
deregulation of other factors controlled by these epi-regulators |
Arabidopsis thaliana |
| down-regulation in the transcript level of the flv4-2 operon |
occurred when |
dysfunctional PBs were present |
Synechocystis |
| regulatory elements |
function in combination to increase |
specificity |
|
| coordinated induction of photosynthetic gene expression in (AQC1, HPS7, TPST, AT1G08030) |
suggests |
suppression of negative regulators for photosynthetic genes |
Arabidopsis thaliana |
| (PRK, AT1G32060) |
is differentially regulated in |
Vaucheria litorea and Elysia chlorotica |
Vaucheria litorea; Elysia chlorotica |
| folate levels |
impact |
expression of other genes |
Solanum lycopersicum |
| chimeric promoter |
could change |
SST expression |
|
| activity of ABC transporters |
might not be regulated at |
transcriptional level |
|
| riboswitches |
control |
gene expression |
|
| Type I and II genes |
regulation is |
primarily post-transcriptional |
|
| histone deacetylase (ATHDA6, AXE1, HDA6, HDAC6, RPD3B, RTS1, SIL1, AT5G63110) |
could represent |
one of those trans-acting determinants |
|
| (ABI3, AtABI3, SIS10, AT3G24650) proteins lacking the B3 domain |
can regulate |
gene expression |
|
| AS2–AS1 complex and putative epigenetic factors |
control |
expression of (ARF3, ETT, AT2G33860) |
Arabidopsis thaliana |
| expression of OsFd1 and OsFdC2 |
are not compensated in |
rice |
Oryza sativa |
| (CCR2, CRTISO, AT1G06820) promoter |
shows atypical reporter gene expression with greater variability compared to |
cauliflower mosaic virus 35S promoter (CaMV35S) |
Arabidopsis thaliana |
| extensive gene silencing of PAL genes in Solanaceae |
precise genetic mechanisms remain to be established |
genetic mechanisms of gene silencing |
Lycopersicon esculentum |
| ARABIDOPSIS THALIANA (BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) (AtGCN5) |
associates with |
large number of promoters |
Arabidopsis thaliana |
| GmCCA1a expression levels |
were more effectively repressed in |
YFP-H4 callus than in YFP-H6 callus |
Glycine max |
| TCP genes |
encode |
transcription factors regulating various target genes |
Arabidopsis thaliana |
| promoter activity of CK2B1 from swollen stem type |
was significantly higher than |
promoter activity of CK2B1 from non-swollen stem types |
Brassica juncea |
| OMTN1, OMTN2, OMTN3, OMTN4 and OMTN6 |
may have different roles in |
OsmiR164 regulatory network |
Oryza sativa |
| RNA trafficking |
has implications in |
systemic regulation of gene expression |
|
| male-transmitted miRNAs |
could mediate regulation of |
transcripts in seed |
Arabidopsis thaliana |
| (CCR2, CRTISO, AT1G06820) promoter |
shows atypical reporter gene expression with greater variability compared to |
εLCY promoter |
Arabidopsis thaliana |
| increased SST expression |
might be caused by |
differential expression of trans-acting factors in Pna-10 and Pna-17 backgrounds |
|
| PHYTOCHROME INTERACTING FACTOR 3 (PAP3, PIF3, POC1, AT1G09530) |
plays central role in |
gene regulatory network |
|
| FAD-binding polyamine oxidase (PAO) genes |
are predicted to be regulated by |
biotic signals |
Arabidopsis thaliana |
| regulation of differentially expressed genes |
is essential for understanding |
developmental processes and environmental stimulations in living organisms |
|
| increased BrLhcb1 expression in (ARK3, AtKINUa, PAK, AT1G12430) choi hybrids |
is caused by |
upregulation of BrCCA1 |
Brassica rapa subsp. chinensis |
| BrCCA1 (CIRCADIAN CLOCK ASSOCIATED 1) |
can directly activate |
BrLhcb1 transcription |
Brassica rapa subsp. chinensis |
| environmentally dependent phenotypic variation |
must involve |
regulation of transcription factors that switch designated gene networks on and off |
|
| double CCR/ (ATCAD4, CAD, CAD-C, CAD4, AT3G19450) down-regulated tobacco plants |
show large modifications of |
gene expression |
Nicotiana tabacum |
| GmPRR3b H6 |
is less effective than GmPRR3b H4 in |
repressing GmCCA1a transcription |
Glycine max |
| GSL metabolites |
may influence |
gene expression |
|
| BrCCA1-silenced (ARK3, AtKINUa, PAK, AT1G12430) choi |
show lower |
BrLhcb1 transcription |
Brassica rapa subsp. chinensis |
| nuclear body |
in which regulators are concentrated could contribute to regulation via |
spatial positioning |
|
| functional interaction between histone methyltransferases, demethylases, and AtGCN5 |
is important for understanding |
genome function |
Arabidopsis thaliana |
| alpha-gliadin genes |
may have |
different promoter regions |
Triticum aestivum |
| acs2-2 promoter |
harbours two mutations in |
promoter |
Solanum lycopersicum |
| AtGCN5 |
may nucleate histone deacetylation on |
core promoters |
Arabidopsis thaliana |
| (ATPAL1, PAL1, AT2G37040) (ATPAL2, PAL2, AT3G53260) mutant |
shows normal size despite |
dramatic perturbation of gene expression |
Arabidopsis thaliana |
| members of the canonical LAFL network |
has been speculated to perform |
reactivation of seed maturation genes in desiccating leaves |
|
| genic coexpression network analyses |
may derive insights into |
physiological responses of diploid versus polyploid cotton |
Gossypium |
| unexpectedly high number of flg22-downregulated genes |
may include |
many indirect targets |
|
| NblA expression |
is adjusted by |
sensor NblS |
cyanobacteria |
| (AtLHP1, LHP1, TFL2, AT5G17690) background |
detected increased levels of |
SEEDKEEPING (AGL11, STK, AT4G09960) |
Arabidopsis thaliana |
| transcription factors |
direct expression reprogramming of |
gene expression |
|
| specific localization of genes |
may affect |
processes other than transcription |
|
| genes |
interact with |
other genes |
|
| H6-YFP overexpression callus |
showed |
significantly downregulated GmCCA1a expression |
Glycine max |
| high-throughput profiling and transcriptional network inference methods |
reveal |
functional interactions across genes |
|
| OsmiR164 |
temporally and spatially regulated |
OsNAM expression pattern |
Oryza sativa |
| non-presence/absence (non-PAV) single-parent expression (SPE) genes |
are under |
trans regulation |
Zea mays |
| primary and secondary signals |
involve changes in |
global gene expression |
|
| gene regulatory networks (GRNs) |
can represent |
spatial regulations |
|
| histone modifications and chromatin accessibility and transcription |
are steps in |
environmental regulation of gene activity |
|
| transcriptional and cis-regulatory state analysis |
crucial to link |
cis-regulatory mechanisms |
|
| expression patterns of StSP6A and StCEN |
closely match |
each other |
Solanum tuberosum |
| (EEP1, MIR164, MIR164C, AT5G27807) |
restricts |
(ANAC098, ATCUC2, CUC2, AT5G53950) expression |
Arabidopsis thaliana |
| regulatory elements |
support |
organ-specific and development-specific functions |
Arabidopsis thaliana |
| transcript abundance of Fe-deficiency-induced genes |
is positively correlated with |
24-nucleotide siRNAs |
Oryza sativa |
| miR171 expression |
can be regulated by |
several different genes and environmental factors |
|
| FAD-binding polyamine oxidase (PAO) genes |
are predicted to be regulated by |
abiotic signals |
Arabidopsis thaliana |
| jaw-D mutants |
have |
(JAW, MIR319, MIR319A, AT4G23713) gene ectopically activated by enhancer cassette promoter |
Arabidopsis thaliana |
| FSH or a FSH-derived molecule |
may act as |
transcription factors |
|
| differences in enzyme activities during the developmental stages |
emphasize |
CaMV 35S promoter is constitutive but is regulated developmentally |
|
| miR171 |
was found to target |
transcription factors involved in regulation of gene expression and signal transduction |
|
| HSFs |
function in |
differential regulation of HSP genes under various environmental stresses and developmental stages |
|
| lack of change in rubisco expression |
may be due to |
high background expression of the rubisco small subunit or rubisco activity is regulated at the protein level rather than at the transcription level |
|
| regulatory npcRNAs |
have been discovered and characterized |
regulatory function |
|
| TE-siR815 |
represses |
(AtSOT1, AtSOT12, ATST1, AtSULT202A1, RAR047, SOT12, ST, ST1, SULT202A1, AT2G03760) expression |
Oryza sativa |
| global analyses of patterns of gene expression downstream of (AS2, AT1G65620) and (AtMORC4, MORC4, AT5G50780) (AtMORC7, MORC7, AT4G24970) |
showed that |
(AS2, AT1G65620) and (AtMORC4, MORC4, AT5G50780) (AtMORC7, MORC7, AT4G24970) regulate different sets of genes |
Arabidopsis thaliana |
| increased BrLhcb1 expression in (ARK3, AtKINUa, PAK, AT1G12430) choi hybrids |
is not caused by |
DNA methylation |
Brassica rapa subsp. chinensis |
| InLYP1 promoter |
contains |
cis-elements involved in light or drought response |
Arabidopsis thaliana |
| methylation of histone H3 lysine 27 (H3K27) |
associates with |
gene silencing |
|
| expression profiling of OtsA- and OtsB-expressing Arabidopsis seedlings |
demonstrated |
TREHALOSE-6-PHOSPHATE (T6P) levels inversely correlate with (AKIN10, KIN10, SnRK1, SnRK1α1, SNRK1.1, AT3G01090) /11-controlled gene expression |
Arabidopsis thaliana |
| Arabidopsis lines down-regulated for C3'H |
display massive changes in |
gene expression |
Arabidopsis thaliana |
| mutations in class I and class II BPCs |
increased |
(ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) expression in roots |
Arabidopsis thaliana |
| upregulation of AGAMOUS (AG) in (AtLHP1, LHP1, TFL2, AT5G17690) (ATBPC4, BBR, BPC4, AT2G21240) (ATBPC6, BBR/BPC6, BPC6, AT5G42520) triple mutant |
confirms |
LHP1–class II BPC interplay in seedlings |
Arabidopsis thaliana |
| (ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) mutants |
show increased acetylation on |
core and upstream promoter regions |
Arabidopsis thaliana |
| long npcRNAs |
modulate |
cellular RNP networks |
|
| AMPK regulation |
includes |
direct activation of transcriptional machinery |
Mammalia |
| gene regulatory network |
consists of |
circadian rhythm-related genes, phytochrome-mediated light signaling-related genes, and stress-tolerance-related genes |
|
| cotton fiber development networks |
demonstrated |
utility of genic coexpression network analyses |
Gossypium |
| ccc mutant |
shows down-regulation of |
(ALDH1A, ALDH2C4, REF1, AT3G24503) gene |
Arabidopsis thaliana |
| new gene clusters |
changing and modifying |
the existing gene transcriptional network |
|
| cold acclimation (CA) |
is |
multigenetically regulated process |
|
| RNA silencing |
is |
conserved mechanism for gene regulation |
|
| combination of bpc alleles |
showed |
pleiotropic phenotypes |
Arabidopsis thaliana |
| HAM expression patterning |
is conserved in |
meristems |
|
| RNA silencing |
is |
pan-eukaryotic, sequence-specific gene regulation mechanism |
|
| TAL effectors |
can be used for |
targeted gene regulation |
|
| timing of regulatory events at different levels |
is |
critical aspect of gene regulation |
|
| heritable stress effects on TS–GUS |
are mediated by |
one or more trans-acting factors |
|
| (MIR171C, AT1G62035) |
targets |
SCL6 genes |
|
| histone acetylation |
has been linked to |
transcriptional control |
|
| ABA |
regulates |
transcriptional gene regulation |
|
| some non-protein-coding RNAs |
have sequence complementary to |
(AHG1, AT5G51760) |
Arabidopsis thaliana |
| non-coding RNAs |
may have |
many species-specific regulatory functions |
|
| genes that co-expressed in the same tissues at the same developmental stages |
may be |
differentially regulated |
|
| 2,825 protein-coding genes |
may be linked to |
differentially expressed lncRNAs |
Solanum lycopersicum |
| expression of OsFd1 and OsFdC2 |
are coordinated in |
rice |
Oryza sativa |
| expression profiles of these genes |
compared using TomExpress, we found a strong Pearson correlation (about 0.9) between them, indicating that |
these genes display very similar transcriptional regulation |
|
| DNA methylation within the gene body at CG, CHG and CHH contexts |
were more robust predictors for gene expression compared with |
promoter and downstream methylation |
Solanum lycopersicum |
| methylation levels within genes |
were not correlated with |
gene expression levels in all genes |
Zea mays |
| TE-induced mutations |
include |
changes in gene regulation by inactivating enhancers or repressors upon insertion |
|
| RNA modifications |
constitute |
essential layer of gene regulation |
|
| within and pan-species comparisons |
illuminate |
deeply conserved circuitry |
|
| uORFs |
is |
variation in RNA sequence determinants |
|
| gene activity |
can be heavily controlled by |
circadian clock |
|
| transcription factors |
are investigated via |
genomic, bioinformatic, and proteomic approaches |
|
| HISTONE DEACETYLASE 9 (AtHDA9, AtHDAC9, HDA09, HDA9, HDAC9, AT3G44680) |
contributes to repression of |
many genes |
|
| mechanisms that assess cell size |
inform |
gene expression |
|
| male-derived (MIR159, MIR159A, AT1G73687) |
acts transgenerationally targeting |
transcription factors (ATMYB33, MYB33, AT5G06100) /65 |
Arabidopsis thaliana |
| (COB, ATMG00220) family members |
are present in |
primary, secondary, and (CESA09, CESA9, AT2G21770) regulons |
Arabidopsis thaliana |
| gene compartmentalization |
may regulate |
transcription |
|
| AMPK regulation |
includes |
stimulation of activators |
Mammalia |
| histone methylation |
has been linked to |
transcriptional control |
|
| competing computational approaches |
highlight |
complex nature of gene regulation |
|
| other regulatory factors instead of promoter |
may cause |
specific expression of CpMYB1 |
Chimonanthus praecox |
| analysis |
detected |
slight enrichment in chromatin marks associated with active transcription at MITE copies positively correlated with copy number increase |
Oryza sativa |
| epigenetic marks |
have strong influence on |
expression of the genome |
|
| meristematic cells |
activate and maintain |
gene expression programs |
|
| gene co-expression networks |
is explored to |
uncover gene regulatory relationships |
|
| microRNAs (miRNAs) |
play pivotal roles in regulating |
gene expression |
|
| candidate functional SNPs |
may be from |
DNA-RNA binding sites |
|
| osmtd2-2 mutant anthers |
show upregulation of genes involved in |
transcriptional modification |
Oryza sativa |
| (ACG1, ATMSI4, FVE, MSI4, NFC04, NFC4, AT2G19520) |
has |
RdDM-independent role |
|
| non-coding RNA (ncRNA) |
can have regulatory effects through direct effects on |
transcription |
|
| AtNF-YA5 gene |
partially overlaps with |
neighbor gene in reverse orientation |
Arabidopsis thaliana |
| inverted repeats |
trigger |
methylation of PAI genes |
Arabidopsis thaliana |
| microRNAs (miRNAs) |
is |
regulatory small RNA class |
|
| ccc mutant |
shows overexpression of |
(CAD1, PROSCOOP5, AT5G44570) gene |
Arabidopsis thaliana |
| chimeric phS:yfp gene |
is terminated by |
endogenous Volvox carteri phS terminator region |
Volvox carteri |
| unintended changes |
could be materialized because of |
position effect |
|
| frameshift mutation of CpMYB1 |
may lead to loss of |
regulatory function of CpMYB1 |
Chimonanthus praecox |
| PAV genes between (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) and Mo17 |
are controlled by |
trans-eQTL |
Zea mays |
| MITE insertions in promoters |
repress |
transcription |
|
| histone methylation |
does not directly lead to |
transcriptional activation or repression |
|
| UPE-box |
is present in |
UP9C promoter |
Nicotiana tabacum |
| AtEIL4 and AtEIL5 |
have not been identified |
characterized functions |
Arabidopsis thaliana |
| TGACG motif |
is found in |
SCP1 promoter |
Oryza sativa |
| (MIR159, MIR159A, AT1G73687) |
has P-box motif in promoter region of |
1000 bp upstream promoter region |
|
| unknown cis-acting element(s) |
may be necessary for |
specific responsiveness to AZC |
Oryza sativa |
| AZRE |
was indispensable for |
HS activation of Oshsp17.3 and Oshsp18.0 |
Oryza sativa |
| (GAUT13, AT3G01040) or (GAUT14, AT5G15470) |
may be partially rescued by |
existing (GAUT12, IRX8, LGT6, AT5G54690) expression |
|
| (PRL1, SCPR44, AT4G15900) mutation |
results in changes in |
gene expression |
Arabidopsis thaliana |
| chromatin-remodeling factors |
may be directly or indirectly involved in activation or repression of |
target genes |
Arabidopsis thaliana |
| nucleolar association of genes |
opens the way for |
spatial positioning via nucleolar positioning |
|
| FLOWERING SEED 3 (FUS3, AT3G26790) |
has been characterized as |
BPC target |
Arabidopsis thaliana |
| drastic decrease of cell wall Rha |
might result from |
altered transcriptional activity |
|
| transcription factors |
play prominent roles in |
regulating expression of genes |
|
| comprehensive understanding of gene regulation mechanisms |
requires more work to build |
gene regulation |
|
| structural variants |
have been suggested to be associated with |
gene regulatory variation in maize |
Zea mays |
| small RNAs |
function as negative regulators of |
gene expression |
|
| TAL effectors |
enable |
control over gene function and expression |
|
| trait-associated SNPs in maize nested association mapping (NAM) population |
approximately half located in |
upstream promoter regions of genes |
Zea mays |
| small, non-coding RNAs (sRNAs) |
participate in |
genetic networks |
|
| microRNAs (miRNAs) |
participate in |
regulatory networks |
|
| technological advances |
have expanded understanding of |
roles transposons play in gene regulation |
|
| TE insertions |
may have |
minor effect on transcription |
|
| circular RNAs (circRNAs) |
represent |
epigenetic regulation |
|
| (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) |
negatively regulates expression of |
(ATFD1, FD1, AT1G10960) |
|
| regulation of (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) |
is |
complicated network that occurs at diverse layers |
|
| PpERF105 |
modulates expression of |
transcription factor genes |
Pyrus pyrifolia |
| ame tool |
found the highest number of motifs in |
C BS and C BS&M (n = 44 and 91, respectively) |
Oryza sativa |
| transcriptional regulation |
involves |
transposable elements |
|
| small RNAs |
negatively regulate |
gene expression |
|
| regular host genes (RHGs) |
have nearly unlimited access to |
novel regulatory cassettes |
|
| TE regulation of genes |
may be more prevalent in |
rice |
Oryza sativa |
| transposable element (TE) insertions |
have regulatory effect on |
adjacent genes |
|
| DNA methylation |
could enhance transcription by promoting the binding of |
transcription activators |
|
| transcription factors |
will likely reveal |
genetic and epigenetic regulation of the P450 gene |
|
| MITE insertions |
repress |
translation |
|
| recent MITE insertions tightly linked to genes |
may be involved in |
differences of gene expression among varieties |
Oryza sativa |
| genetic and molecular analyses in Arabidopsis thaliana |
shed light on |
regulatory networks in plants |
Arabidopsis thaliana |
| small RNAs (sRNAs) |
includes |
micro RNAs (miRNAs) |
|
| artificial eccDNA |
can express |
small regulatory RNAs |
|
| Trans-regulation of memory genes |
implicates mechanisms such as |
non-coding RNAs |
|
| second allele associated with Ps-DACS3b |
was found only in |
late SH genotype |
Prunus spp. |
| high cysteine proteinase activities in OCE leaves |
indicates the presence of |
feedback modulation of cysteine proteinase expression |
Nicotiana tabacum |
| T/G-box element (AACGTG) |
is present at |
-226 to -221 |
Gossypium arboreum |
| proximal RY elements |
comprise |
ABA response elements (ABREs) |
Arabidopsis thaliana |
| upstream regions of (ATCYTC-A, CYTC-1, AT1G22840) and (CYTC-2, AT4G10040) genes |
produce |
partially different expression patterns |
Arabidopsis thaliana |
| increase in transcript levels of MtPIM |
triggers |
strong repression of MtFULc |
Medicago truncatula |
| non-PAV SPE genes |
are predominantly under |
cis regulation |
Zea mays |
| analyses of conserved non-coding regions |
identified |
putative cis-regulatory sequences |
|
| small RNAs |
regulate |
gene expression |
|
| cell functionality |
can be compared with |
gene expression |
|
| histone methylation |
elevates or lowers |
transcriptional competence of genes |
|
| biogenic signaling |
acts through |
chromatin remodeling |
|
| bromodomain-acetylated histone interaction |
may be required for |
basal transcription |
Arabidopsis thaliana |
| microRNAs (miRNAs) |
are |
post-transcriptional negative regulators |
|
| ABA |
regulates |
post-transcriptional gene regulation |
|
| (ATRALF1, RALF1, RALFL1, AT1G02900) promoter |
contains |
RH-specific cis-element (RHE) |
Arabidopsis thaliana |
| abscisic acid |
impacts |
abundance of gene transcripts |
|
| GmNF-YC4 |
might be able to bind directly to |
promoter region of asparagine synthetase-related genes |
Glycine max |
| coding regions of ZmMYB138 and ZmMYB115 |
were amplified with |
Zma-miR159k-3p binding sites |
Zea mays |
| small interfering RNAs (siRNAs) |
mediate |
gene expression |
|
| integration of different data types |
reveals |
detailed knowledge of gene regulatory networks |
|
| Trans-regulation of memory genes |
implicates mechanisms such as |
long-range interactions between (ATNACK2, NACK2, TES, AT3G43210) and memory genes |
|
| methylation levels within genes |
negatively correlates with |
transcript abundance of starch synthesis genes |
Zea mays |
| PAV genes between (B73, CHL6, CNX, CNX1, SIR4, AT5G20990) and Mo17 |
are controlled by |
cis-eQTL |
Zea mays |
| some MITE insertions |
may modify |
gene expression |
Oryza sativa |
| fimo tool |
identified the most enriched motifs in |
C V and C BS&M (n = 86 and 100, respectively) |
Oryza sativa |
| paramutations |
involve |
trans-homolog interactions |
|
| small RNAs |
play important roles in |
biological processes |
|
| epigenetic modifications |
reprogram |
gene expression networks |
|
| modification of epigenetic marks and distal regulatory regions |
regulates |
gene expression |
|
| important signal molecules |
modify |
gene expression |
|
| ethylene perception |
was not required for |
superinduction of PhPT1 by CHX |
|
| another JA-independent signal |
is also needed for |
NaF6ʹH1 activation |
Nicotiana attenuata |
| large haplotype-specific structural variants |
have potential to affect |
allele-specific expression |
Manihot esculenta |
| (SUVH1, AT5G04940) binding |
enhanced |
proximal gene transcription |
Arabidopsis thaliana |
| (DDP1, PTM, AT5G35210) in the nucleus |
was suggested to activate |
ABA INSENSITIVE 4 (ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) |
|
| vein-specific transcription factors |
included families such as |
(AtbZIP, bZIP, AT1G68880) (bHLH, AT5G51780) G2-like, MYB-related and Dof |
Oryza sativa |
| japonica background |
more readily facilitates |
Xa3/Xa26 expression |
Oryza sativa |
| cis-regulatory element presence and accessibility |
is |
specific regulatory feature |
|
| β-cyclocitral (β-CC) |
is able to regulate |
gene expression |
|
| phylostratigraphy |
is explored to |
uncover gene regulatory relationships |
|
| changes in chromatin accessibility |
can influence activation or repression of |
specific genes |
|
| H3K4me2 |
is implicated with |
activation and possibly repression |
Arabidopsis thaliana; Oryza sativa |
| microRNAs |
are |
endogenously produced 21-nt riboregulators |
|
| gene regulatory networks (GRNs) |
are used to visualize |
causal regulatory relationships between regulators and their downstream target genes |
|
| complex interplay at overlapping RNAPII/III-transcribed genes |
exists in |
Arabidopsis thaliana |
Arabidopsis thaliana |
| PIP (plant-inducible promoter) box |
is upstream of |
protease genes |
Xanthomonas |
| distant eQTLs |
tend to form |
hotspots in the genome, controlling genes significantly enriched in specific functional categories and being trans-regulators for a variety of metabolic pathways |
Zea mays |
| altering the abundance of SlSCL3 protein |
may lead to |
different stable state with increased activation of genes downstream of SlSCL3 |
Solanum lycopersicum |
| 19.61% of analyzed genes |
were associated with |
trans-only regulation |
Oryza minuta |
| H3K27me2 in mouse |
plays |
protective role in preventing the activation of non-cell-type-specific enhancer elements |
Mus musculus |
| high PpMYB140 expression level after 1-MCP treatment |
might be regulated by |
other transcription factors |
Pyrus pyrifolia |
| transcriptional activation of transcription factors |
was not triggered by |
demethylation |
Zea mays |
| amplification loop |
control |
gene expression |
|
| transcription factors and chromatin remodeling elements |
identified in |
plasticity-linked genes and plasticity-specific candidate genes |
Medicago truncatula |
| deep learning models |
can predict |
transcription factor binding |
|
| HISTONE DEACETYLASE 9 (AtHDA9, AtHDAC9, HDA09, HDA9, HDAC9, AT3G44680) |
can function in |
transcriptional activation |
|
| gene expression |
is transcriptionally regulated by |
cis-acting regulatory elements |
|
| regulation of (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) |
includes |
transcription, epigenetic regulation and post-translational modifications |
|
| 16.67% of analyzed genes |
were associated with |
cis-only regulation |
Oryza minuta |
| genome sequences |
enable understanding of |
gene regulatory landscapes in plants |
|
| mobile RNAs |
function as |
gene regulatory molecules |
|
| increased SST expression |
may be due to |
chimeric promoter itself |
|
| expression of a large number of genes |
appears unaffected by |
nuclear positioning |
|