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SRX4893319: GSM3431731: dim5_LP_K4_rep1; Neurospora crassa; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 32M spots, 1.6G bases, 1.3Gb downloads

Submitted by: NCBI (GEO)
Study: Context dependent Histone H3 Lysine 4 methylation is necessary for repression and is a requisite modification for facultative heterochromatin at distinct loci [ChIP-seq]
show Abstracthide Abstract
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. Nor is know how specific chromatin-modifiers assist in modulating the light response or the extent of the defects in strains lacking certain chromatin modifications. Using a combination of RNA-seq and ChIP-seq we examines H3K4 methylation and H3K9 methylation and found paradigm changing properties beyond the consensus that H3K4me3 is a solely a mark for activation and H3K9me3 marks silent heterochromatin domains. Overall design: Samples consist of different strains, harvest times, and antibodies.
Sample: dim5_LP_K4_rep1
SAMN10247578 • SRS3940304 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: Tissue was crosslinked with 1% formaldehyde. The purified DNA was sent to Beijing Genome Institute (BGI) for library preparation and sequencing. The samples were sequenced to a depth of 50 million 50-bp single-end read.
Experiment attributes:
GEO Accession: GSM3431731
Links:
Runs: 1 run, 32M spots, 1.6G bases, 1.3Gb
Run# of Spots# of BasesSizePublished
SRR806496131,973,0841.6G1.3Gb2018-11-30

ID:
6593808

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