U.S. flag

An official website of the United States government

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO DataSets

Items: 20

1.

Caenorhabditis briggsae SDC-2 and DPY-27 ChIP-seq

(Submitter supplied) ChIP-seq for the SDC-2 and DPY-27 subunits of the dosage compensation complex in C. briggsae
Organism:
Caenorhabditis briggsae
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL27110
10 Samples
Download data: BW
Series
Accession:
GSE214714
ID:
200214714
2.

SDC-3 subunit of the dosage compensation complex in wild-type N2 C. elegans and Hi-C in C' elegans strains with deleted rex and extra rex sites

(Submitter supplied) ChIP-seq for the SDC-3 subunit of the dosage compensation complex in wild-type N2 C. elegans and Hi-C in C' elegans strains with deleted rex and extra rex sites
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL22765 GPL13776
6 Samples
Download data: BED, MATRIX, TXT
Series
Accession:
GSE205949
ID:
200205949
3.

DCC binding and function (ChIP-chip: SDC-3, DPY-27, Mock)

(Submitter supplied) In many species, a dosage compensation complex (DCC) is targeted to X chromosomes of one sex to equalize levels of X gene products between males (1X) and females (2X). Here we identify cis-acting regulatory elements that target the C. elegans X chromosome for repression by the DCC. The DCC binds to discrete, dispersed sites on X of two types. rex sites recruit the DCC in an autonomous, DNA sequence-dependent manner using a 12 bp consensus motif that is enriched on X. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8135
5 Samples
Download data: GFF, PAIR
Series
Accession:
GSE14653
ID:
200014653
4.

DCC binding and function (ChIP-chip: SDC-2)

(Submitter supplied) In many species, a dosage compensation complex (DCC) is targeted to X chromosomes of one sex to equalize levels of X gene products between males (1X) and females (2X). Here we identify cis-acting regulatory elements that target the C. elegans X chromosome for repression by the DCC. The DCC binds to discrete, dispersed sites on X of two types. rex sites recruit the DCC in an autonomous, DNA sequence-dependent manner using a 12 bp consensus motif that is enriched on X. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8134
2 Samples
Download data: GFF, PAIR
Series
Accession:
GSE14652
ID:
200014652
5.

DCC binding and function (ChIP-chip: DPY-27)

(Submitter supplied) In many species, a dosage compensation complex (DCC) is targeted to X chromosomes of one sex to equalize levels of X gene products between males (1X) and females (2X). Here we identify cis-acting regulatory elements that target the C. elegans X chromosome for repression by the DCC. The DCC binds to discrete, dispersed sites on X of two types. rex sites recruit the DCC in an autonomous, DNA sequence-dependent manner using a 12 bp consensus motif that is enriched on X. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7098
1 Sample
Download data: GFF, PAIR
Series
Accession:
GSE14651
ID:
200014651
6.

DCC binding and function (ChIP-chip: SDC-3, MIX-1, DPY-27, Mock)

(Submitter supplied) In many species, a dosage compensation complex (DCC) is targeted to X chromosomes of one sex to equalize levels of X gene products between males (1X) and females (2X). Here we identify cis-acting regulatory elements that target the C. elegans X chromosome for repression by the DCC. The DCC binds to discrete, dispersed sites on X of two types. rex sites recruit the DCC in an autonomous, DNA sequence-dependent manner using a 12 bp consensus motif that is enriched on X. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8133
8 Samples
Download data: GFF, TXT
Series
Accession:
GSE14650
ID:
200014650
7.

DCC binding and function (Expression Analysis)

(Submitter supplied) In many species, a dosage compensation complex (DCC) is targeted to X chromosomes of one sex to equalize levels of X gene products between males (1X) and females (2X). Here we identify cis-acting regulatory elements that target the C. elegans X chromosome for repression by the DCC. The DCC binds to discrete, dispersed sites on X of two types. rex sites recruit the DCC in an autonomous, DNA sequence-dependent manner using a 12 bp consensus motif that is enriched on X. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
26 Samples
Download data: CEL
Series
Accession:
GSE14649
ID:
200014649
8.

A condensin-like dosage compensation complex acts at a distance to control expression throughout the genome

(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
5 related Platforms
42 Samples
Download data: CEL, GFF, PAIR, PDF, TXT
Series
Accession:
GSE14640
ID:
200014640
9.

Condensin-Driven Remodeling of X-Chromosome Topology during Dosage Compensation [Hi-C]

(Submitter supplied) The three-dimensional (3D) organization of a genome plays a critical role in regulating gene expression, yet little is known about the machinery and mechanisms that determine higher-order chromosome structure or how structure influences gene expression. Here we exploit the X-chromosome-wide process of dosage compensation to dissect these mechanisms. The dosage compensation complex (DCC) of C. elegans, a condensin complex, binds to both X chromosomes of hermaphrodites via sequence-specific recruitment sites (rex sites) to reduce chromosome-wide gene expression by half. more...
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL18245
2 Samples
Download data: TAR, XLS
Series
Accession:
GSE63717
ID:
200063717
10.

Condensin-Driven Remodeling of X-Chromosome Topology during Dosage Compensation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL18245 GPL13657
13 Samples
Download data: TAR
Series
Accession:
GSE59716
ID:
200059716
11.

Condensin-Driven Remodeling of X-Chromosome Topology during Dosage Compensation [RNA-Seq]

(Submitter supplied) The three-dimensional (3D) organization of a genome plays a critical role in regulating gene expression, yet little is known about the machinery and mechanisms that determine higher-order chromosome structure or how structure influences gene expression. Here we exploit the X-chromosome-wide process of dosage compensation to dissect these mechanisms. The dosage compensation complex (DCC) of C. elegans, a condensin complex, binds to both X chromosomes of hermaphrodites via sequence-specific recruitment sites (rex sites) to reduce chromosome-wide gene expression by half. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13657
7 Samples
Download data: CSV
Series
Accession:
GSE59715
ID:
200059715
12.

Condensin-Driven Remodeling of X-Chromosome Topology during Dosage Compensation [ChIP-Seq]

(Submitter supplied) The three-dimensional (3D) organization of a genome plays a critical role in regulating gene expression, yet little is known about the machinery and mechanisms that determine higher-order chromosome structure or how structure influences gene expression. Here we exploit the X-chromosome-wide process of dosage compensation to dissect these mechanisms. The dosage compensation complex (DCC) of C. elegans, a condensin complex, binds to both X chromosomes of hermaphrodites via sequence-specific recruitment sites (rex sites) to reduce chromosome-wide gene expression by half. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL13657
4 Samples
Download data: GFF
Series
Accession:
GSE59597
ID:
200059597
13.

Comparison of DPY-27 binding in embryos and fed L1 larvae

(Submitter supplied) Here we exploit the essential process of X-chromosome dosage compensation to elucidate basic mechanisms that control the assembly, genome-wide binding, and function of gene regulatory complexes that act over large chromosomal territories. We demonstrate that a subunit of C. elegans MLL/COMPASS, a gene-activation complex, acts within the dosage compensation complex (DCC), a condensin complex, to target the DCC to both X chromosomes of hermaphrodites and thereby reduce chromosome-wide gene expression. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8134
3 Samples
Download data: GFF, PAIR
Series
Accession:
GSE25877
ID:
200025877
14.

An MLL/COMPASS subunit functions in the C. elegans dosage compensation complex to target X chromosomes for transcriptional regulation of gene expression

(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:
GPL200 GPL8134
53 Samples
Download data: CEL, CHP, GFF, PAIR
Series
Accession:
GSE25834
ID:
200025834
15.

Examination of DPY-30, DPY-27, SDC-3, DPY-26, MIX-1, SMC-4, ASH-2, RNA Polymerase II binding in wild type and DCC mutant embryos

(Submitter supplied) Here we exploit the essential process of X-chromosome dosage compensation to elucidate basic mechanisms that control the assembly, genome-wide binding, and function of gene regulatory complexes that act over large chromosomal territories. We demonstrate that a subunit of C. elegans MLL/COMPASS, a gene-activation complex, acts within the dosage compensation complex (DCC), a condensin complex, to target the DCC to both X chromosomes of hermaphrodites and thereby reduce chromosome-wide gene expression. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8134
44 Samples
Download data: GFF, PAIR
Series
Accession:
GSE25833
ID:
200025833
16.

Fed L1 larvae total RNA levels by microarray

(Submitter supplied) Here we exploit the essential process of X‐chromosome dosage compensation to elucidate basic mechanisms that control the assembly, genome‐wide binding, and function of gene regulatory complexes that act over large chromosomal territories. We demonstrate that a subunit of C. elegans MLL/COMPASS, a gene-activation complex, acts within the dosage compensation complex (DCC), a condensin complex, to target the DCC to both X chromosomes of hermaphrodites and thereby reduce chromosome-wide gene expression. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE25831
ID:
200025831
17.

Examination of DPY-30, DPY-27, SDC-3, DPY-26, DPY-28, SDC-2, and SUMOylated DPY-27 binding in wild type embryos and smo-1 RNAi treated embryos

(Submitter supplied) The essential process of dosage compensation equalizes X-chromosome gene expression between C. elegans XO males and XX hermaphrodites through a dosage compensation complex (DCC) that resembles condensin. The DCC binds to both X chromosomes of hermaphrodites to repress transcription by half. Here we show that post-translational modification by the SUMO conjugation pathway is essential for sex-specific assembly of the DCC onto X. more...
Organism:
Caenorhabditis elegans
Type:
Genome variation profiling by genome tiling array
Platforms:
GPL8135 GPL8134
35 Samples
Download data: GFF, PAIR
Series
Accession:
GSE48413
ID:
200048413
18.

C. elegans mixed stage embryo total RNA levels by microarray: L4440 RNAi, smo-1 RNAi and sdc-2 (y93)+RNAi

(Submitter supplied) The essential process of dosage compensation equalizes X-chromosome gene expression between C. elegans XO males and XX hermaphrodites through a dosage compensation complex (DCC) that resembles condensin. The DCC binds to both X chromosomes of hermaphrodites to repress transcription by half. Here we show that post-translational modification by the SUMO conjugation pathway is essential for sex-specific assembly of the DCC onto X. more...
Organism:
Caenorhabditis elegans
Type:
Expression profiling by array
Platform:
GPL200
9 Samples
Download data: CEL, CHP
Series
Accession:
GSE48347
ID:
200048347
19.

X chromosome domain architecture regulates Caenorhabditis elegans lifespan but not dosage compensation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL22765
26 Samples
Download data: BW, MATRIX, TXT
Series
Accession:
GSE128568
ID:
200128568
20.

Binding of an X-specific condensin correlates with a reduction in active histone modifications at gene regulatory elements

(Submitter supplied) Condensins are evolutionarily conserved protein complexes that are required for chromosome segregation during cell division and genome organization during interphase. In C. elegans, a specialized condensin, which forms the core of the dosage compensation complex (DCC), binds to and represses X chromosome transcription. Here, we analyzed DCC localization and the effect of DCC depletion on histone modifications, transcription factor binding, and gene expression using ChIP-seq and mRNA-seq. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing
5 related Platforms
169 Samples
Download data: TXT
Series
Accession:
GSE122639
ID:
200122639
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

db=gds|term=|query=1|qty=3|blobid=MCID_675cf5120600166e51455cfb|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
   Taxonomic Groups  [List]
Tree placeholder
    Top Organisms  [Tree]

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center