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Links from GEO DataSets

Items: 20

1.

MES-4, an autosome-associated HMT that participates in silencing the X chromosomes in the C. elegans germ line

(Submitter supplied) Microarray-based expression profiling of dissected gonads from mes-4 mutants reveals that MES-4 is required to repress expression of a set of X-linked genes. Keywords: Mutant analysis of mes-4 in dissected C. elegans gonads
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL3860
4 Samples
Download data
Series
Accession:
GSE5454
ID:
200005454
2.

Expression profiling in N2 (wild-type) early embryo

(Submitter supplied) Determination of gene expression levels in wild-type early embryo. First published in Rechtsteiner et al. 2010 PLoS Genetics.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL18856
4 Samples
Download data: PAIR, TXT
Series
Accession:
GSE58759
ID:
200058759
3.

LMN-1-DamID in N2 and set-25(n5021) met-2(n4256) mutant early C. elegans embryos

(Submitter supplied) We asked if the perinuclear position of chromosome arms in C. elegans depends on the histone methyltransferases MET-2 and SET-25. To this end, we performed LMN-1-DamID in wild-type (N2) and mutant (set-25 met-2) strains. LMN-1-DamID signal on chromosome arms was significantly reduced in the mutant.
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL8134
6 Samples
Download data: PAIR, TAB
Series
Accession:
GSE37226
ID:
200037226
4.

DRM complex mutant lin-54 vs. H3K36 methyltransferase mutant mes-4 vs. lin-54; mes-4 double mutant vs. wild type C.elegans germline

(Submitter supplied) Here we uncover antagonistic regulation of transcript levels in the germline of Caenorhabditis elegans hermaphrodites. The histone methyltransferase MES-4 marks genes expressed in the germline with methylated Lys36 on histone H3 (H3K36me) and promotes their transcription; MES-4 also represses genes normally expressed in somatic cells and genes on the X chromosomes. The DRM complex, which includes E2F/DP and Retinoblastoma homologs, affects germline gene expression and prevents excessive repression of X-chromosome genes. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
12 Samples
Download data: CEL
Series
Accession:
GSE52064
ID:
200052064
5.

Strome Mes-4, H3K36me3 and H3K27me3 in N2 EEMB

(Submitter supplied) ChIP-chip of Mes-4, H3K36me3 and H3K27me3 in N2 C. elegans early embryo
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8647
8 Samples
Download data: PAIR
Series
Accession:
GSE38180
ID:
200038180
6.

Transcript and chromatin analysis in mes-2, mes-4, and mes-2; mes-4 double mutants

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL5883 GPL8647
25 Samples
Download data: GPR, PAIR
Series
Accession:
GSE38160
ID:
200038160
7.

Strome MES-4, H3K36me3 and H3K27me3 in mes-4 RNAi EEMB

(Submitter supplied) ChIP-chip of MES-4, H3K36me3 and H3K27me3 in mes-4 RNAi C. elegans early embryo
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8647
5 Samples
Download data: PAIR
Series
Accession:
GSE38159
ID:
200038159
8.

mes-2, mes-4 or mes-2; mes-4 mutants vs. wild type

(Submitter supplied) Trascriptional profiling of C. elegans adult germ lines comparing mes-2(bn11)unc-4(e120) mutants and unc-4(e120) (wild type), mes-4(bn85) mutants and N2 (wild type), mes-2(bn11)unc-4(e120); mes-4(bn85) and unc-4(e120) (wild type) at 20 degrees.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL5883
12 Samples
Download data: GPR
Series
Accession:
GSE38158
ID:
200038158
9.

Bisection of the X Chromosome Disrupts the Initiation of Chromosome Silencing during Meiosis in Caenorhabditis elegans

(Submitter supplied) During meiosis, gene expression is silenced in aberrantly unsynapsed chromatin and in heterogametic sex chromosomes. Initiation of sex chromosome silencing is disrupted in meiocytes with sex chromosome-autosome translocations. To determine whether this is due to aberrant synapsis or loss of continuity of sex chromosomes, we engineered Caenorhabditis elegans with non-translocated, bisected X chromosomes. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL19757
2 Samples
Download data: XLSX
Series
Accession:
GSE171938
ID:
200171938
10.

Decoupling the downstream effects of germline nuclear RNAi reveals that transcriptional repression and heritable RNAi are independent of the H3K9me3 response in C. elegans

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platform:
GPL13657
40 Samples
Download data
Series
Accession:
GSE86517
ID:
200086517
11.

Decoupling the downstream effects of germline nuclear RNAi reveals that transcriptional repression and heritable RNAi are independent of the H3K9me3 response in C. elegans [pre-mRNA-seq]

(Submitter supplied) Germline nuclear RNAi in C. elegans is a transgenerational gene-silencing pathway that leads to the H3K9 trimethylation (H3K9me3) response and transcriptional repression of target genes. The H3K9me3 response induced either by exogenous dsRNA or endogenous siRNA (endo-siRNA) is highly specific to the target loci and transgenerationally heritable. Despite these features, the role of H3K9me3 in transcriptional repression and heritable gene silencing at native target genes has not been tested. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
5 Samples
Download data: XLSX
Series
Accession:
GSE86516
ID:
200086516
12.

Decoupling the downstream effects of germline nuclear RNAi reveals that transcriptional repression and heritable RNAi are independent of the H3K9me3 response in C. elegans [RNA-seq]

(Submitter supplied) Germline nuclear RNAi in C. elegans is a transgenerational gene-silencing pathway that leads to the H3K9 trimethylation (H3K9me3) response and transcriptional repression of target genes. The H3K9me3 response induced either by exogenous dsRNA or endogenous siRNA (endo-siRNA) is highly specific to the target loci and transgenerationally heritable. Despite these features, the role of H3K9me3 in transcriptional repression and heritable gene silencing at native target genes has not been tested. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
5 Samples
Download data: XLSX
Series
Accession:
GSE86515
ID:
200086515
13.

Decoupling the downstream effects of germline nuclear RNAi reveals that transcriptional repression and heritable RNAi are independent of the H3K9me3 response in C. elegans [ChIP-seq]

(Submitter supplied) Germline nuclear RNAi in C. elegans is a transgenerational gene-silencing pathway that leads to the H3K9 trimethylation (H3K9me3) response and transcriptional repression of target genes. The H3K9me3 response induced either by exogenous dsRNA or endogenous siRNA (endo-siRNA) is highly specific to the target loci and transgenerationally heritable. Despite these features, the role of H3K9me3 in transcriptional repression and heritable gene silencing at native target genes has not been tested. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13657
30 Samples
Download data: XLSX
Series
Accession:
GSE86513
ID:
200086513
14.

Members of the H3K4 trimethylation complex regulate lifespan in a germline-dependent manner in C. elegans

(Submitter supplied) The plasticity of ageing suggests that longevity may be controlled epigenetically by specific alterations in chromatin state. The link between chromatin and ageing has mostly focused on histone deacetylation by the Sir2 family1, 2, but less is known about the role of other histone modifications in longevity. Histone methylation has a crucial role in development and in maintaining stem cell pluripotency in mammals3. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Datasets:
GDS4575 GDS5012
Platform:
GPL200
23 Samples
Download data: CEL
Series
Accession:
GSE30505
ID:
200030505
15.
Full record GDS5012

ash-2 knockdown effect on germline-deficient glp-1(e2141ts) mutant: day 8 (mid-life stage)

Analysis of day 8 germline-deficient glp-1 mutants treated with ash-2 RNAi. The ASH-2 trithorax complex trimethylates histone H3 at lysine 4 (H3K4); an intact germline is required for ASH-2-induced lifespan extension. Results provide insight into the role of histone methylation in longevity.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, transformed count, 2 genotype/variation, 2 protocol sets
Platform:
GPL200
Series:
GSE30505
11 Samples
Download data: CEL
16.
Full record GDS4575

ash-2 knockdown effect on germline-deficient glp-1(e2141ts) mutant: day 2 (L3 stage)

Analysis of day 2 germline-deficient glp-1 mutants treated with ash-2 RNAi. The ASH-2 trithorax complex trimethylates histone H3 at lysine 4 (H3K4); an intact germline is required for ASH-2-induced lifespan extension. Results provide insight into the role of histone methylation in longevity.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array, transformed count, 2 genotype/variation, 2 protocol sets
Platform:
GPL200
Series:
GSE30505
12 Samples
Download data: CEL
17.

Maternal H3K36 and H3K27 HMTs protect germline development via regulation of the transcription factor LIN-15B

(Submitter supplied) Maternally synthesized products play critical roles in development of offspring. A premier example is the C. elegans H3K36 methyltransferase MES-4, which is essential for germline survival and development in offspring. How maternal MES-4 protects the germline is not well understood, but its role in H3K36 methylation hinted that it may regulate gene expression in Primordial Germ Cells (PGCs). We tested this hypothesis by profiling transcripts from nascent germlines (PGCs and their descendants) dissected from wild-type and mes-4 mutant (lacking maternal and zygotic MES-4) larvae. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18245 GPL26672
132 Samples
Download data: TXT
Series
Accession:
GSE198552
ID:
200198552
18.

Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18245
99 Samples
Download data
Series
Accession:
GSE156551
ID:
200156551
19.

Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (smallRNA-seq)

(Submitter supplied) The establishment and maintenance of chromatin domains shape the epigenetic memory of a cell, with histone H3 lysine 9 methylation defining repressed heterochromatin. We show that in C. elegans the SET-25 (SUV39/G9a) HMT that catalyzes H3K9me1-3, is able to establish repressed domains de novo. We identify here two distinct pathways that recruit SET-25 to its targets. One requires LIN-61 (L3MBTL2), a conserved protein with 4 MBT domains that recognizes H3K9me2 deposited by the HMT MET-2 (SETDB1). more...
Organism:
Caenorhabditis elegans
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL18245
18 Samples
Download data: TAB
Series
Accession:
GSE156550
ID:
200156550
20.

Two parallel pathways recruit the H3K9me3 HMT in somatic cells, requiring the Argonaut NRDE-3, or the MBT-domain protein, LIN-61 (RNA-seq)

(Submitter supplied) The establishment and maintenance of chromatin domains shape the epigenetic memory of a cell, with histone H3 lysine 9 methylation defining repressed heterochromatin. We show that in C. elegans the SET-25 (SUV39/G9a) HMT that catalyzes H3K9me1-3, is able to establish repressed domains de novo. We identify here two distinct pathways that recruit SET-25 to its targets. One requires LIN-61 (L3MBTL2), a conserved protein with 4 MBT domains that recognizes H3K9me2 deposited by the HMT MET-2 (SETDB1). more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18245
21 Samples
Download data: TAB
Series
Accession:
GSE156549
ID:
200156549
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