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Links from GEO DataSets

Items: 20

1.

Evolutionary conservation of nuclear lamina-genome interactions

(Submitter supplied) Regulation of gene expression is highly conserved between vertebrates, yet the genomic binding patterns of transcription factors are poorly conserved, suggesting that other mechanisms may contribute. The spatial organization of chromosomes in the nucleus is known to affect gene activity, but it is unclear to what extent this organization is conserved in evolution. Genome-wide maps of nuclear lamina (NL) interactions show that human and mouse chromosomes have highly similar folding patterns inside the nucleus. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
6 Samples
Download data: PAIR, TXT
Series
Accession:
GSE22428
ID:
200022428
2.

DamID LaminB1 data in mouse MEFs, wild-type and POU2F1-/-. DamID LaminA data in mouse Neural Precursor Cells and Astrocytes.

(Submitter supplied) DamID LaminB1 data were generated in POU2F1-/- MEFs to study the potential role of POU2F1/Oct1 in genome - nuclear lamina interactions. DamID LaminA data were generated in NPCs and Astrocytes to study similarities/differences between LaminA and LaminB1 binding. The procedure to arrive at the provided Hidden Markov Model (HMM) state calls is as follows: We fitted a two-state HMM whereby emissions are distributed as Student's t variables. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8840
8 Samples
Download data: PAIR, TXT
Series
Accession:
GSE36132
ID:
200036132
3.

Stochastic genome-nuclear lamina interactions: Modulating roles of Lamin A and BAF

(Submitter supplied) The nuclear lamina (NL) is a filamentous layer lining the inner-nuclear-membrane (INM) that aids in the organization of the genome in large domains of low transcriptional activity. Recently, it was shown that the single-cell genome-NL interactions are much more dynamic than previously anticipated, which challenges the concept of the NL as a safe guard for transcriptional repressed genes. Here we discuss the role of the NL in light of these new findings and introduce Lamin A and BAF as potential modulators of LAD positioning
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
4 Samples
Download data: PAIR, TXT
Series
Accession:
GSE55066
ID:
200055066
4.

Characterization of the dynamics of lamin A and lamin B LADs in HepG2 cells: impact of cyclosporin A

(Submitter supplied) Purpose: to qualify and quantify the rearrangement of interactions of nuclear lamins A/C and B with the genome, in relation to nuclearradial repositioning of loci and changes in gene expression, in HepG2 cells exposed to cyclosporin A. .To compare HepG2 cell line transcriptome profiling (RNA-seq) with radially positioning of the chromatin anchored at the nuclear periphery before and after CsA treatment. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16791
8 Samples
Download data: BED, BEDGRAPH, FPKM_TRACKING
5.

Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions

(Submitter supplied) Proper genome functionality is underpinned by the non-random, spatial or ganisation of chromatin. At the periphery of the nucleus, the association of chr omatin with the nuclear lamina is thought to facilitate both structural organisa tion and regulation of gene expression. Except for a small number of individual loci, the regions of the human genome that locate at the nuclear lamina have not been identified. more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
9 related Platforms
10 Samples
Download data: TSV, TXT
Series
Accession:
GSE8854
ID:
200008854
6.

Massive reshaping of genome - nuclear lamina interactions during oncogene induced senescence (genome tiling)

(Submitter supplied) Background. Cellular senescence is a mechanism that virtually irreversibly suppresses the proliferative capacity of cells in response to various stress signals. This includes the expression of activated oncogenes, which cause Oncogene-Induced Senescence (OIS). A body of evidence points to the involvement of chromatin reorganization, including the formation of senescence-associated heterochromatic foci (SAHF). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10559
1 Sample
Download data: PAIR
Series
Accession:
GSE76646
ID:
200076646
7.

Massive reshaping of genome - nuclear lamina interactions during oncogene induced senescence

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL11154 GPL10559
37 Samples
Download data: PAIR
Series
Accession:
GSE76605
ID:
200076605
8.

Massive reshaping of genome - nuclear lamina interactions during oncogene induced senescence (DamID-seq)

(Submitter supplied) Background. Cellular senescence is a mechanism that virtually irreversibly suppresses the proliferative capacity of cells in response to various stress signals. This includes the expression of activated oncogenes, which cause Oncogene-Induced Senescence (OIS). A body of evidence points to the involvement of chromatin reorganization, including the formation of senescence-associated heterochromatic foci (SAHF). more...
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL11154
12 Samples
Download data: CSV, TXT
Series
Accession:
GSE76594
ID:
200076594
9.

Massive reshaping of genome - nuclear lamina interactions during oncogene induced senescence (RNA-seq)

(Submitter supplied) Cellular senescence is a mechanism that virtually irreversibly suppresses the proliferative capacity of cells in response to various stress signals. This includes the expression of activated oncogenes, which cause Oncogene-Induced Senescence (OIS). A body of evidence points to the involvement of chromatin reorganization, including the formation of senescence-associated heterochromatic foci (SAHF). The nuclear lamina (NL) is an important contributor to genome organization and has been involved in cellular senescence and organismal aging. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11154
24 Samples
Download data: TXT
Series
Accession:
GSE75643
ID:
200075643
10.

Reorganization of nuclear lamina – genome interactions upon differentiation of embryonic stem cells.

(Submitter supplied) The three-dimensional organization of chromosomes within the nucleus and its dynamics during differentiation are largely unknown. We present a genome-wide analysis of the interactions between chromatin and the nuclear lamina during differentiation of mouse embryonic stem cells (ESCs) into lineage-committed neural precursor cells (NPCs) and terminally differentiated astrocytes. Chromatin in each of these cell types shows a similar organization into large lamina associated domains (LADs), which represent a transcriptionally repressive environment. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8840
8 Samples
Download data: BED, PAIR, TXT
Series
Accession:
GSE17051
ID:
200017051
11.

Genome-wide maps of nuclear lamina interactions in AML12 cells.

(Submitter supplied) We have used microarrays to identify LaminB1 occupancy signal in AML12 cell using the DamID protocol.
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL10448
4 Samples
Download data: TXT
Series
Accession:
GSE73703
ID:
200073703
12.

Nuclear Lamins are Not Required for Genome Organization in Mouse Embryonic Stem Cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL8840 GPL13112
15 Samples
Download data: PAIR
Series
Accession:
GSE62685
ID:
200062685
13.

Nuclear Lamins are Not Required for Genome Organization in Mouse Embryonic Stem Cells [RNA-Seq]

(Submitter supplied) In mammals, the nuclear lamina interacts with hundreds of large genomic regions, termed lamina-associated domains (LADs) that are generally in a transcriptionally repressed state. Lamins form the major structural component of the lamina and have been reported to bind DNA and chromatin. Here we systematically evaluated whether lamins are necessary for the peripheral localization of LADs in murine embryonic stem cells. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: TXT
Series
Accession:
GSE62684
ID:
200062684
14.

Nuclear Lamins are Not Required for Genome Organization in Mouse Embryonic Stem Cells [DamID]

(Submitter supplied) In mammals, the nuclear lamina interacts with hundreds of large genomic regions, termed lamina-associated domains (LADs) that are generally in a transcriptionally repressed state. Lamins form the major structural component of the lamina and have been reported to bind DNA and chromatin. Here we systematically evaluated whether lamins are necessary for the peripheral localization of LADs in murine embryonic stem cells. more...
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8840
11 Samples
Download data: PAIR, TXT
Series
Accession:
GSE62683
ID:
200062683
15.

The insulator protein SU(HW) modulates nuclear lamina interactions of the Drosophila genome

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by genome tiling array; Expression profiling by array
Platforms:
GPL6952 GPL8471
25 Samples
Download data: PAIR, TXT
Series
Accession:
GSE20313
ID:
200020313
16.

The insulator protein SU(HW) modulates nuclear lamina interactions of the Drosophila genome: expression

(Submitter supplied) Specific interactions of the genome with the nuclear lamina (NL) are thought to assist chromosome folding inside the nucleus and to contribute to the regulation of gene expression. High-resolution mapping has recently identified hundreds of large, sharply defined lamina-associated domains (LADs) in the human genome, and suggested that the insulator protein CTCF may help to demarcate these domains. Here, we report the detailed structure of LADs in Drosophila cells, and investigate the putative roles of five insulator proteins in LAD organization. more...
Organism:
Drosophila melanogaster
Type:
Expression profiling by array
Platform:
GPL6952
3 Samples
Download data: TXT
Series
Accession:
GSE20312
ID:
200020312
17.

The insulator protein SU(HW) modulates nuclear lamina interactions of the Drosophila genome: DamID

(Submitter supplied) Specific interactions of the genome with the nuclear lamina (NL) are thought to assist chromosome folding inside the nucleus and to contribute to the regulation of gene expression. High-resolution mapping has recently identified hundreds of large, sharply defined lamina-associated domains (LADs) in the human genome, and suggested that the insulator protein CTCF may help to demarcate these domains. Here, we report the detailed structure of LADs in Drosophila cells, and investigate the putative roles of five insulator proteins in LAD organization. more...
Organism:
Drosophila melanogaster
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL8471
22 Samples
Download data: PAIR, TXT
Series
Accession:
GSE20311
ID:
200020311
18.

DamID (LmnB1/Dam) Log2 ratios of C57Bl/6 fibroblasts and RAG2-/- pro-B cells.

(Submitter supplied) Comparison of DamID profiles and LAD patterning across cell types reveals regions of variable LADs
Organism:
Mus musculus
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL7525
4 Samples
Download data: BEDGRAPH, PAIR
Series
Accession:
GSE56990
ID:
200056990
19.

Local euchromatin enrichment in lamina-associated domains anticipates their re-positioning in the adipogenic lineage

(Submitter supplied) Interactions of chromatin with the nuclear lamina via lamina-associated domains (LADs) confers structural stability to the genome. The dynamics of positioning of LADs during differentiation, and how LADs impinge on developmental gene expression, remains elusive, however. We examined changes in the association of lamin B1 with the genome in the first 72 hours of differentiation of adipose stem cells into adipocytes. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL24676 GPL20301 GPL18573
82 Samples
Download data: BED, BEDGRAPH, BROADPEAK, BW, NARROWPEAK, TXT
20.

Genome-wide maps of nuclear lamina interactions in single human cells. (Hi-C, KBM7 haploid)

(Submitter supplied) Mammalian interphase chromosomes interact with the nuclear lamina (NL) through hundreds of large Lamina Associated Domains (LADs). We report a method to map NL contacts genome-wide in single human cells. Analysis of ~400 maps reveals a core architecture of gene-poor LADs that contact the NL with high cell-to-cell consistency, interspersed by LADs with more variable NL interactions. The variable contacts are more sensitive to a change in genome ploidy than the consistent contacts. more...
Organism:
Homo sapiens
Type:
Other
Platform:
GPL11154
2 Samples
Download data: TXT
Series
Accession:
GSE69841
ID:
200069841
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