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.

Nucleic Acids Research
|March 25, 2022
PubMed

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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