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Links from GEO DataSets

Items: 20

1.

Histone deacetylation and cytosine methylation are required for the normal compartmentalization of heterochromatin in the genome organization of Neurospora crassa

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platforms:
GPL23150 GPL26551
31 Samples
Download data: BEDGRAPH, BIGWIG, BW, H5
Series
Accession:
GSE232935
ID:
200232935
2.

Histone deacetylation and cytosine methylation are required for the normal compartmentalization of heterochromatin in the genome organization of Neurospora crassa [Hi-C]

(Submitter supplied) Chromosomes must correctly fold in eukaryotic nuclei for proper genome function. Eukaryotic organisms hierarchically organize their genomes: in the fungus Neurospora crassa, chromatin fiber loops compact into Topologically Associated Domain (TAD)-like structures that are anchored by heterochromatic region aggregates. However, insufficient information exists on how histone post-translational modifications, including acetylation, impact genome organization. more...
Organism:
Neurospora crassa
Type:
Other
Platforms:
GPL23150 GPL26551
12 Samples
Download data: H5
Series
Accession:
GSE232934
ID:
200232934
3.

Histone deacetylation and cytosine methylation are required for the normal compartmentalization of heterochromatin in the genome organization of Neurospora crassa [ChIP-Seq]

(Submitter supplied) Chromosomes must correctly fold in eukaryotic nuclei for proper genome function. Eukaryotic organisms hierarchically organize their genomes: in the fungus Neurospora crassa, chromatin fiber loops compact into Topologically Associated Domain (TAD)-like structures that are anchored by heterochromatic region aggregates. However, insufficient information exists on how histone post-translational modifications, including acetylation, impact genome organization. more...
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26551
19 Samples
Download data: BEDGRAPH, BIGWIG, BW
Series
Accession:
GSE232933
ID:
200232933
4.

Dual chromatin recognition by the histone deacetylase complex HCHC is required for proper DNA methylation in Neurospora crassa

(Submitter supplied) Whole-Genome Bisulfite Sequencing of HCHC mutants To extend our understanding of the role of the HCHC complex in Neurospora, we carried out whole-genome bisulfite sequencing (WGBS) of cdp-2, chap, and hda-1 mutants.  Consistent with prior analyses, the WGBS revealed both hypomethylated and hypermethylated regions in the three HCHC mutants while the ; sequences with a lower Combined RIP Index (CRI) tend to show reduced methylation in the mutants, while sequences with higher CRI scores show increased methylation. more...
Organism:
Neurospora crassa
Type:
Methylation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16164
7 Samples
Download data: IGV, TDF
Series
Accession:
GSE81129
ID:
200081129
5.

Genome-wide maps of H3K9me3 with tethered heterochromatin machinery

(Submitter supplied) Purpose: The goal of this study is to characterize the domain(s) of H3K9me3 induced by artifical localization of heterochromatin factors in wild-type and mutant backgrounds.
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL23150
6 Samples
Download data: TDF, TXT
Series
Accession:
GSE103926
ID:
200103926
6.

HiC of Wild Type Neurospora crassa and mutants deficient in heterochromatin formation

(Submitter supplied) Eukaryotic genomes are organized into chromatin domains with distinct three-dimensional arrangements resulting from nucleic acid and protein factor interactions within the physical constraints of the nucleus. It is of obvious interest to determine interactions between various chromosomal regions defined by these nuclear constraints, and to identify important factors that limit the interactions. We used chromosome conformation capture (3C) followed by high-throughput sequencing (HiC) to improve our understanding of Neurospora crassa genome organization and to examine if known components of heterochromatin machinery influence nuclear organization. more...
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL20705
5 Samples
Download data: FASTA, GTF, TDF, TXT
Series
Accession:
GSE71024
ID:
200071024
7.

Relics of repeat-induced point mutation direct heterochromatin formation in Neurospora crassa

(Submitter supplied) Both RNAi-dependent and -independent mechanisms have been implicated in the establishment of heterochromatin domains, which may be stabilized by feedback loops involving chromatin proteins and modifications of histones and DNA. Neurospora crassa sports features of heterochromatin found in higher eukaryotes, namely cytosine methylation (5mC), methylation of histone H3 lysine9 (H3K9me) and HETEROCHROMATIN PROTEIN-1 (HP1), and provides a model to investigate heterochromatin establishment and maintenance. more...
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by genome tiling array; Methylation profiling by genome tiling array
Platform:
GPL7253
13 Samples
Download data: GPR
Series
Accession:
GSE12690
ID:
200012690
8.

Nucleosome Positioning by an Evolutionarily Conserved Chromatin Remodeler Prevents Aberrant DNA Methylation in Neurospora.

(Submitter supplied) Aberrant DNA methylation is often associated with cancers and DNA-demethylating agents such as 5-azacytidine (5-azaC) are often used for anti-tumor therapy. Although it is clinically effective at inhibiting DNA methylation, the mechanistic effect that 5-azaC elicits on eukaryotic cells is controversial. It has been proposed that incorporation of 5-azaC into DNA during replication irreversibly tethers cytosine methyltransferases (MTases) to DNA. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing; Genome variation profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL20660 GPL16164
19 Samples
Download data: FASTA, IGV, TDF, TXT, VCF, WIG
Series
Accession:
GSE98911
ID:
200098911
9.

The genome organization of Neurospora crassa at high-resolution uncovers principles of fungal chromosome topology

(Submitter supplied) For a eukaryotic genome to properly function, its chromatin must be precisely organized, as genome topology impacts transcriptional regulation, cell division, DNA replication, and DNA repair, among other essential processes. Disruption of human genome topology can lead to disease states, such as cancer. The advent of chromosome conformation capture with high-throughput sequencing (Hi-C) technologies to assess genome organization has revolutionized our understanding of the arrangement of chromosomes within the nuclear genome. more...
Organism:
Neurospora crassa
Type:
Other
Platforms:
GPL26551 GPL23150
10 Samples
Download data: FASTA, GTF, H5
Series
Accession:
GSE173593
ID:
200173593
10.

Loss of Lysine-Specific Demethylase 1 (LSD1) Drives Aberrant Heterochromatin Formation in Neurospora crassa

(Submitter supplied) Both H3K9me3 and DNA methylation are subject to spreading mechanisms to effectively cover incipient chromatin across heterochromatin domains. Boundary elements and associated limiting factors are necessary to prevent heterochromatin from spreading into neighboring, gene-rich heterochromatin. LSD1 was identified to be one such factor, given previous studies in other models and high conservation throughout eukaryotes. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing; Third-party reanalysis
Platforms:
GPL23150 GPL20660 GPL16164
16 Samples
Download data: BED, BIGWIG, IGV, TDF, TXT
Series
Accession:
GSE137018
ID:
200137018
11.

Neurospora crassa genome organization requires subtelomeric facultative heterochromatin

(Submitter supplied) Facultative heterochromatin in the filamentous fungus Neurospora crassa is identified by the repressive histone mark H3K27me3 and is primarily subtelomeric, while constitutive heterochromatin, marked by the DIM-5-catalzyed H3K9me3, is found at centromeres, telomeres, and smaller dispersed regions. In strains lacking constitutive heterochromatin (e.g., Δdim-5), H3K27me2/3 relocalizes to the regions formerly marked by H3K9me3. more...
Organism:
Neurospora crassa
Type:
Other; Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing
Platforms:
GPL20705 GPL20660
16 Samples
Download data: BCF, FASTA, GTF, TDF, TXT, XLSX
Series
Accession:
GSE82222
ID:
200082222
12.

Neurospora importin alpha compromises H3K9me3 and cytosine methylation levels through inappropriate localization of the heterochromatin machinery

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL16164
5 Samples
Download data: TDF, WIG
Series
Accession:
GSE61175
ID:
200061175
13.

Bisulfite-seq from Neurospora crassa a wild type (WT) strain grown in minimum medium, a dim-3 strain grown in minimum medium, and a dim-3 strain grown with supplemented histidine

(Submitter supplied) We report the placement of cytosine methylation from the filamentous fungus Neurospora crassa in wild type and dim-3 strains by bisulfite-sequencing. Compared to a wild type strain, the dim-3 strain has a global reduction in cytosine methylation, and this reduction in cytosine methylation is exacerbated by the supplementation of histidine to the growth medium. This global reduction in cytosine methylation results from a causative mutation in importin alpha (NUP-6), a component of the nuclear transport machinery, which severely reduces the level of the heterochromatic mark H3K9me3. more...
Organism:
Neurospora crassa
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL16164
3 Samples
Download data: WIG
Series
Accession:
GSE61174
ID:
200061174
14.

H3K9me3 ChIP-seq from Neurospora crassa wild type (WT) and dim-3 (severely reduced H3K9me3 levels) strains

(Submitter supplied) We report the placement of the H3K9me3 heterochromatin mark from the filamentous fungus Neurospora crassa in wild type and dim-3 strains. The dim-3 strain has a global reduction in H3K9me3, which results from a causative mutation in importin alpha (NUP-6), a component of the nuclear transport machinery. NUP-6(dim-3) compromises the heterochromatic localization of several components of the DCDC, a histone H3K9 methyltransferase complex, from their sub-nuclear chromatin targets despite appropriate nuclear transport. more...
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16164
2 Samples
Download data: TDF
Series
Accession:
GSE61173
ID:
200061173
15.

Context dependent Histone H3 Lysine 4 methylation is necessary for repression and is a requisite modification for facultative heterochromatin at distinct loci

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20705
32 Samples
Download data
Series
Accession:
GSE121356
ID:
200121356
16.

Context dependent Histone H3 Lysine 4 methylation is necessary for repression and is a requisite modification for facultative heterochromatin at distinct loci [RNA-seq]

(Submitter supplied) Sensing and responding to light provides organisms an adaptive advantage, in part by altering gene expression. The complement of light-activated genes in model organisms is largely known, and some of the mechanisms by which proteins modulate the light response are likewise well defined. However, how light alters post translation modifications to chromatin and how changes in chromatin facilitates and/or inhibit changes in gene expression has not been examined in depth. more...
Organism:
Neurospora crassa
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20705
12 Samples
Download data: FPKM_TRACKING, GTF
Series
Accession:
GSE121353
ID:
200121353
17.

Context dependent Histone H3 Lysine 4 methylation is necessary for repression and is a requisite modification for facultative heterochromatin at distinct loci [ChIP-seq]

(Submitter supplied) Sensing and responding to light provides organisms an adaptive advantage, in part by altering gene expression. The complement of light-activated genes in model organisms is largely known, and some of the mechanisms by which proteins modulate the light response are likewise well defined. However, how light alters post translation modifications to chromatin and how changes in chromatin facilitates and/or inhibit changes in gene expression has not been examined in depth. more...
Organism:
Neurospora crassa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL20705
20 Samples
Download data: BED
Series
Accession:
GSE121333
ID:
200121333
18.

Histone H3K9 methylation promotes formation of genome compartments in C. elegans via chromosome compaction and perinuclear anchoring

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing; Other
Platform:
GPL22765
8 Samples
Download data: BW, TXT
Series
Accession:
GSE144253
ID:
200144253
19.

Histone H3K9 methylation promotes formation of genome compartments in C. elegans via chromosome compaction and perinuclear anchoring (Hi-C)

(Submitter supplied) Genomic regions preferentially associate with regions of similar transcriptional activity, partitioning genomes into active and inactive compartments within the nucleus. Here we explored mechanisms controlling genome compartment organization in C. elegans and investigated roles for compartments in regulating gene expression. The distal arms of C. elegans chromosomes, which are enriched for heterochromatic histone modifications including H3K9me, interact with each other both in cis and in trans, while interacting less frequently with central regions of chromosomes, leading to genome compartmentalization. more...
Organism:
Caenorhabditis elegans
Type:
Other
Platform:
GPL22765
2 Samples
Download data: TXT
Series
Accession:
GSE144252
ID:
200144252
20.

Histone H3K9 methylation promotes formation of genome compartments in C. elegans via chromosome compaction and perinuclear anchoring (ChIP-seq)

(Submitter supplied) Genomic regions preferentially associate with regions of similar transcriptional activity, partitioning genomes into active and inactive compartments within the nucleus. Here we explored mechanisms controlling genome compartment organization in C. elegans and investigated roles for compartments in regulating gene expression. The distal arms of C. elegans chromosomes, which are enriched for heterochromatic histone modifications including H3K9me, interact with each other both in cis and in trans, while interacting less frequently with central regions of chromosomes, leading to genome compartmentalization. more...
Organism:
Caenorhabditis elegans
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL22765
6 Samples
Download data: BW
Series
Accession:
GSE144251
ID:
200144251
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