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Links from GEO DataSets

Items: 20

1.

An evaluation of the effects of CRISPR/cas9-mediated editing of the Dxz4 locus on regulation of the mouse inactive X chromosome in Patski cells [ChIP-seq]

(Submitter supplied) The mammalian inactive X chromosome (Xi) condenses into a bipartite structure with two superdomains of frequent long-range contacts separated by a boundary or hinge region. Using in situ DNase Hi-C in mouse cells with deletions or inversions within the hinge, we show that the conserved repeat locus Dxz4 alone is sufficient to maintain the bipartite structure and that Dxz4 orientation controls the distribution of long-range contacts on the Xi. more...
Organism:
Mus musculus x Mus spretus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20213
6 Samples
Download data: BED, XLS
Series
Accession:
GSE107286
ID:
200107286
2.

An evaluation of the effects of CRISPR/cas9-mediated editing of the Dxz4 locus on regulation of the mouse inactive X chromosome in Patski cells [RNA-seq]

(Submitter supplied) The mammalian inactive X chromosome (Xi) condenses into a bipartite structure with two superdomains of frequent long-range contacts separated by a boundary or hinge region. Using in situ DNase Hi-C in mouse cells with deletions or inversions within the hinge, we show that the conserved repeat locus Dxz4 alone is sufficient to maintain the bipartite structure and that Dxz4 orientation controls the distribution of long-range contacts on the Xi. more...
Organism:
Mus musculus x Mus spretus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20213
17 Samples
Download data: TSV
Series
Accession:
GSE107291
ID:
200107291
3.

An evaluation of the effects of CRISPR/cas9-mediated editing of the Dxz4 locus on regulation of the mouse inactive X chromosome in Patski cells [ATAC-seq]

(Submitter supplied) The mammalian inactive X chromosome (Xi) condenses into a bipartite structure with two superdomains of frequent long-range contacts separated by a boundary or hinge region. Using in situ DNase Hi-C in mouse cells with deletions or inversions within the hinge, we show that the conserved repeat locus Dxz4 alone is sufficient to maintain the bipartite structure and that Dxz4 orientation controls the distribution of long-range contacts on the Xi. more...
Organism:
Mus musculus x Mus spretus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20213
4 Samples
Download data: BED, XLS
Series
Accession:
GSE107290
ID:
200107290
4.

An evaluation of the effects of CRISPR/cas9-mediated editing of the Dxz4 locus on regulation of the mouse inactive X chromosome in Patski cells [DNase HiC]

(Submitter supplied) The mammalian inactive X chromosome (Xi) condenses into a bipartite structure with two superdomains of frequent long-range contacts separated by a boundary or hinge region. Using in situ DNase Hi-C in mouse cells with deletions or inversions within the hinge, we show that the conserved repeat locus Dxz4 alone is sufficient to maintain the bipartite structure and that Dxz4 orientation controls the distribution of long-range contacts on the Xi. more...
Organism:
Mus musculus x Mus spretus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20213
6 Samples
Download data: TXT
Series
Accession:
GSE107282
ID:
200107282
5.

Nucleophosmin binding on the mouse X chromosomes

(Submitter supplied) In mammals, one of the female X chromosomes and all imprinted genes are expressed exclusively from a single allele in somatic cells. To evaluate structural changes associated with allelic silencing, we have applied a recently developed Hi-C assay that uses DNase I for chromatin fragmentation to mouse F1 hybrid systems. Results We find radically different conformations for the two female mouse X chromosomes. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10129
2 Samples
Download data: GFF
Series
Accession:
GSE71903
ID:
200071903
6.

Bipartite structure of the inactive mouse X chromosome

(Submitter supplied) A subset of genomic regions, including one of the female X chromosomes and all imprinted genes, are expressed exclusively from a single allele in somatic cells of mammals. To evaluate structural changes associated with allelic silencing, we used mouse F1 hybrid systems in which X inactivation is skewed and alleles can be distinguished based on single nucleotide polymorphisms to analyze chromatin contacts by a new Hi-C assay that uses DNase I for chromatin fragmentation. more...
Organism:
Mus musculus x Mus spretus
Type:
Other
Platforms:
GPL16616 GPL20213
4 Samples
Download data: TXT
Series
Accession:
GSE68992
ID:
200068992
7.

Female-specific CTCF binding on the inactive X chromosome in mouse

(Submitter supplied) In mammals, genes located on the X chromosome are present in one copy in XY males and two in XX females. To balance the dosage of X-linked gene expression between the sexes one of the two X chromosomes in females is silenced by X inactivation initiated by up-regulation of the lncRNA (long non-coding RNA) Xist and recruitment of specific chromatin modifiers for silencing. The inactivated X chromosome becomes heterochromatic and visits a specific nuclear compartment adjacent to the nucleolus. more...
Organism:
Mus musculus x Mus spretus; Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
5 related Platforms
19 Samples
Download data: GFF, PAIR
Series
Accession:
GSE66262
ID:
200066262
8.

Effects of Firre knockdown on mouse gene expression

(Submitter supplied) In mammals, genes located on the X chromosome are present in one copy in XY males and two in XX females. To balance the dosage of X-linked gene expression between the sexes one of the two X chromosomes in females is silenced by X inactivation initiated by up-regulation of the lncRNA (long non-coding RNA) Xist and recruitment of specific chromatin modifiers for silencing. The inactivated X chromosome becomes heterochromatic and visits a specific nuclear compartment adjacent to the nucleolus. more...
Organism:
Mus musculus x Mus spretus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16617
4 Samples
Download data: TXT
Series
Accession:
GSE66172
ID:
200066172
9.

Studies of regulation of mouse X inactivation and genes escaping XCI

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Mus musculus x Mus spretus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Other
9 related Platforms
70 Samples
Download data: BED, BIGWIG, GFF, PAIR, TXT, XLS
Series
Accession:
GSE59779
ID:
200059779
10.

Regulation of mouse X inactivation (ChIP-Seq)

(Submitter supplied) X chromosome inactivation (XCI) silences most genes on one X chromosome in female mammals, but some genes escape XCI. To identify escape gene in vivo and to explore molecular mechanisms that regulate this process we analyzed the allele-specific expression and chromatin structure of X-linked genes in mouse tissues and cells with skewed XCI and distinguishable alleles based on single nucleotide polymorphisms. more...
Organism:
Mus musculus x Mus spretus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL18997 GPL16617
3 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE59778
ID:
200059778
11.

Escape from X inactivation in mouse tissues (RNA-Seq)

(Submitter supplied) X chromosome inactivation (XCI) silences most genes on one X chromosome in female mammals, but some genes escape XCI. To identify escape gene in vivo and to explore molecular mechanisms that regulate this process we analyzed the allele-specific expression and chromatin structure of X-linked genes in mouse tissues and cells with skewed XCI and distinguishable alleles based on single nucleotide polymorphisms. more...
Organism:
Mus musculus x Mus spretus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16617
5 Samples
Download data: TXT
Series
Accession:
GSE59777
ID:
200059777
12.

Upregulation of the mammalian X chromosome is associated with enhanced transcription initiation, MOF-mediated H4K16 acetylation, and longer RNA half-life

(Submitter supplied) Many animal species employ a chromosome-based mechanism of sex determination, which has led to coordinate evolution of dosage compensation systems. Dosage compensation not only corrects the imbalance in the number of X-chromosomes between the sexes, but is also hypothesized to correct dosage imbalance within cells due to mono-allelic X expression and bi-allelic autosomal expression, by upregulating X-linked genes (termed ‘Ohno’s hypothesis’). more...
Organism:
Mus musculus; Mus musculus x Mus spretus
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL10129 GPL16733 GPL16143
25 Samples
Download data: PAIR
Series
Accession:
GSE44835
ID:
200044835
13.

Allele-specific maps of RNA polymerase II phosphorylated at serine 5 in mouse cultured hybrid cells and mouse hybrid brain

(Submitter supplied) We report the application of single-molecule-based sequencing technology for high-throughput profiling of RNA polymerase II phosphorylated at serine 5 (PolII-S5p; the transcription initiation form) in female mouse cultured hybrid cells and female hybrid brain derived from mouse systems with skewed X inactivation based on crosses between C57BL/6J (BL6) and M. spretus. In these systems, alleles can be differentiated by frequent SNPs between mouse species, and the active X (Xa) compared to the haploid set of autosomes from the same species. more...
Organism:
Mus musculus x Mus spretus
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16616 GPL16617
3 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE44255
ID:
200044255
14.

Expression data from mouse ES cells after control RNAi (scramble siRNAs) or specific RNAi (siRNAs for specific genes) treatment

(Submitter supplied) To address the functional role of MOF in mammalian X upregulation, male and female mouse ES cells were transfected with a mixture of three small interfering RNA duplexes, each of which targets a different region of Mof mRNA. We found that MOF knockdown in mouse ES cells caused a greater drop in expression of X-linked genes compared to autosomal genes, as measured by expression array analyses. The strongest effect was observed on medium-expressed X-linked genes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL6246
27 Samples
Download data: CEL
Series
Accession:
GSE44252
ID:
200044252
15.

Expression data from undifferentiated and differentiated mouse female ES cells PGK12.1

(Submitter supplied) Affymetrix 430 2.0 mouse arrays were used for expression analyses in undifferentiated and differentiated PGK12.1 ES cells. We found that the X:autosome expression ratios calculated from the mean expression values of X-linked and autosomal genes from microarrays was ~1.4 in undifferentiated female ES cells and then decreased to 1.2 in PGK12.1 cells after 15-day embryoid body differentiation. Thus, a substantial level of X upregulation is already evident in these ES cells prior to differentiation. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL1261
2 Samples
Download data: CEL
Series
Accession:
GSE44251
ID:
200044251
16.

Mammalian X upregulation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Mus musculus x Mus spretus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by genome tiling array; Expression profiling by array
9 related Platforms
60 Samples
Download data: BED, BIGWIG, CEL, GFF, PAIR, TXT
Series
Accession:
GSE30761
ID:
200030761
17.

Expression analysis in mouse female PGK12.1 ES cells by RNA-seq

(Submitter supplied) Many animal species employ a chromosome-based mechanism of sex determination, which has led to coordinate evolution of dosage compensation systems. Dosage compensation not only corrects the imbalance in the number of X-chromosomes between the sexes, but is also hypothesized to correct dosage imbalance within cells due to mono-allelic X expression and bi-allelic autosomal expression, by upregulating X-linked genes (termed ‘Ohno’s hypothesis’). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9185
1 Sample
Download data: TXT
Series
Accession:
GSE30690
ID:
200030690
18.

Enrichment profiles of Ser-5 phosphorylated RNA polymerase II (PolII S5p) in mouse female ES cells

(Submitter supplied) Many animal species employ a chromosome-based mechanism of sex determination, which has led to coordinate evolution of dosage compensation systems. Dosage compensation not only corrects the imbalance in the number of X-chromosomes between the sexes, but is also hypothesized to correct dosage imbalance within cells due to mono-allelic X expression and bi-allelic autosomal expression, by upregulating X-linked genes (termed ‘Ohno’s hypothesis’). more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL9833
2 Samples
Download data: GFF, PAIR
Series
Accession:
GSE30689
ID:
200030689
19.

Deletion of DXZ4 on the human inactive X chromosome eliminates superdomains and impairs gene silencing

(Submitter supplied) During interphase, the inactive X chromosome (Xi) adopts an unusual 3D configuration known as the Barr body and is largely transcriptionally silent. Despite the importance of X inactivation, little is known about the 3D configuration of Xi and its relationship to gene silencing. We recently showed that in humans, Xi exhibits two distinctive structural features. First, Xi is partitioned into two huge intervals, called superdomains, such that pairs of loci in each superdomain show an enhanced contact frequency with one another. more...
Organism:
Macaca mulatta; Homo sapiens; Mus musculus
Type:
Other; Expression profiling by high throughput sequencing
5 related Platforms
101 Samples
Download data: HIC, PDF, TSV, TXT
Series
Accession:
GSE71831
ID:
200071831
20.

Structural organization of the inactive X chromosome

(Submitter supplied) X-chromosome inactivation (XCI) entails a massive structural reorganization of the inactive X (Xi). However the molecular architecture of the Xi is unknown. Here we show that the Xi lacks typical autosomal features such as active/inactive compartments and topologically associating domains (TADs), except around a small number of genes that escape XCI and remain expressed. Escaping genes form TADs and retain DNA accessibility at promoter-proximal and CTCF binding sites, indicating that these loci can avoid Xist-mediated erasure of chromosomal structure. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Other; Third-party reanalysis
Platform:
GPL13112
8 Samples
Download data: TAR, TXT
Series
Accession:
GSE72697
ID:
200072697
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