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Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
Published on: January 26, 2018
H3K56 deacetylation and H2A.Z deposition are required for aberrant heterochromatin spreading
Chengcheng Zhang1, Yuan Tian1, Shuang Song2
1State Key Laboratory of Agrobiotechnology and MOA Key Laboratory of Soil Microbiology, College of Biological Sciences, China Agricultural University, Beijing 100193, China.
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 upstream of the cat-3 gene, hereby called 5H-cat-3 domain, to constrain aberrant heterochromatin spreading. Interestingly, aberrant spreading of the 5H-cat-3 domain observed in the dmm-1KO strain is accompanied by robust deposition of histone variant H2A.Z, and deletion of H2A.Z abolishes aberrant spreading of the 5H-cat-3 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 5H-cat-3 domain. Importantly, genome-wide analyses demonstrated the general roles of H3K56 deacetylation and H2A.Z deposition in aberrant spreading of heterochromatin. Together, our results illustrate a previously unappreciated regulatory process that mediates aberrant heterochromatin spreading.
Insights
DNA METHYLATION MODULATOR-1 (DMM-1) in Neurospora crassa restricts heterochromatin spreading. Histone variant H2A.Z and H3K56 deacetylation are key regulators, preventing gene silencing.
Area of Science:
- Epigenetics
- Molecular Biology
- Genetics
Background:
- Heterochromatin spreading must be controlled to prevent silencing of essential genes.
- The JmjC domain protein DNA METHYLATION MODULATOR-1 (DMM-1) is known to prevent aberrant heterochromatin spreading in Neurospora crassa, but its mechanism is unclear.
Purpose of the Study:
- To elucidate the molecular mechanisms by which DMM-1 restricts heterochromatin spreading.
- To investigate the roles of histone modifications and variants in heterochromatin boundary maintenance.
Main Methods:
- Chromatin immunoprecipitation to assess protein enrichment and histone modifications.
- Gene deletion and point mutation studies (dmm-1KO, H2A.Z deletion, H3K56Q mutation).
- Genome-wide analyses to identify heterochromatin spreading patterns.
Main Results:
- DMM-1 is enriched in the 5H-cat-3 heterochromatin domain, constraining its spread.
- Aberrant heterochromatin spreading in dmm-1KO strains correlates with H2A.Z deposition.
- H3K56 deacetylation and H2A.Z deposition are general mechanisms involved in heterochromatin spreading.
Conclusions:
- DMM-1 functions to maintain heterochromatin boundaries.
- H2A.Z deposition and H3K56 deacetylation are critical for aberrant heterochromatin spreading.
- This study reveals a novel regulatory process controlling heterochromatin dynamics.
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