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SRX13618024: GSM5772778: H3K56Qdmm-1KO_HP1_input_BMRC210004703-1A; Neurospora crassa; ChIP-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 4.7M spots, 1.4G bases, 435.4Mb downloads

External Id: GSM5772778_r1
Submitted by: Yunnan University
Study: H3K56 deacetylation and H2A.Z deposition are required for aberrant heterochromatin spreading
show Abstracthide Abstract
Crucial mechanisms are required to restrict self-propagating heterochromatin spreading within defined boundaries and prevent euchromatic gene silencing. In the filamentous fungus Neurospora crassa, the JmjC domain protein DNA METHYLATION MODULATOR-1 (DMM-1) prevents aberrant spreading of heterochromatin, but the molecular details remain unknown. Here, we revealed that DMM-1 is highly enriched in a well-defined 5-kb heterochromatin domain and constrained its aberrant spreading. Interestingly, aberrant spreading of the 5-kb heterochromatin domain observed in the dmm-1KO strain is accompanied by the sharp deposition of histone variant H2A.Z, and deletion of H2A.Z abolishes aberrant spreading of the 5-kb heterochromatin domain into adjacent euchromatin. Furthermore, lysine 56 of histone H3 is deacetylated at the expanded heterochromatin regions, and mimicking H3K56 acetylation with an H3K56Q mutation effectively blocks H2A.Z-mediated aberrant spreading of the 5-kb heterochromatin domain. More importantly, genome-wide analyses demonstrated the general roles of H3K56 deacetylation and H2A.Z deposition in aberrant spreading of heterochromatin. Altogether, our results illustrate a previously unappreciated regulatory process that mediates aberrant heterochromatin spreading. Overall design: Dissectingthe molecular mechanisms of ectopic heterochromatin spreading in N. crassa.
Sample: H3K56Qdmm-1KO_HP1_input_BMRC210004703-1A
SAMN24655632 • SRS11507142 • All experiments • All runs
Library:
Name: GSM5772778
Instrument: Illumina NovaSeq 6000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: Lysates were clarified from sonicated mycelia and histone-DNA complexes were isolated with antibody. The purified DNA was used for ChIP-seq library preparation. The library was constructed by Novogene Corporation (Beijing, China). Subsequently, pair-end sequencing of sample was performed on Illumina platform (Illumina, CA, USA). Library quality was assessed on the Agilent Bioanalyzer 2100 system.
Runs: 1 run, 4.7M spots, 1.4G bases, 435.4Mb
Run# of Spots# of BasesSizePublished
SRR174467804,720,8431.4G435.4Mb2022-01-10

ID:
18926663

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