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Reference - PMID:31278118 - Cohesin Impedes Heterochromatin Assembly in Fission Yeast Cells Lacking Pds5.

Reference summary

PubMed ID
PMID:31278118
Title
Cohesin Impedes Heterochromatin Assembly in Fission Yeast Cells Lacking Pds5.
Authors
Folco HD, McCue A, Balachandran V, Grewal SIS
Citation
Genetics 2019 Sep;213(1):127-141
Publication year
2019
Abstract
The fission yeast Schizosaccharomyces pombe is a powerful genetic model system for uncovering fundamental principles of heterochromatin assembly and epigenetic inheritance of chromatin states. Heterochromatin defined by histone H3 lysine 9 methylation and HP1 proteins coats large chromosomal domains at centromeres, telomeres, and the mating-type ( mat ) locus. Although genetic and biochemical studies have provided valuable insights into heterochromatin assembly, many key mechanistic details remain unclear. Here, we use a sensitized reporter system at the mat locus to screen for factors affecting heterochromatic silencing. In addition to known components of heterochromatin assembly pathways, our screen identified eight new factors including the cohesin-associated protein Pds5. We find that Pds5 enriched throughout heterochromatin domains is required for proper maintenance of heterochromatin. This function of Pds5 requires its associated Eso1 acetyltransferase, which is implicated in the acetylation of cohesin. Indeed, introducing an acetylation-mimicking mutation in a cohesin subunit suppresses defects in heterochromatin assembly in pds5 ∆ and eso1 ∆ cells. Our results show that in cells lacking Pds5, cohesin interferes with heterochromatin assembly. Supporting this, eliminating cohesin from the mat locus in the pds5 ∆ mutant restores both heterochromatin assembly and gene silencing. These analyses highlight an unexpected requirement for Pds5 in ensuring proper coordination between cohesin and heterochromatin factors to effectively maintain gene silencing.

Annotation

GO cellular component

GO:0000785 - chromatin

Genes:

GO:0099115 - chromosome, subtelomeric region

Genes:

GO:0031934 - mating-type region heterochromatin

Genes:

GO:0005721 - pericentric heterochromatin

Genes:

Multi-locus phenotype

FYPO:0002827 - decreased chromatin silencing at silent mating-type cassette

Genes:

Genotypes:

FYPO:0006670 - meiotic cell cycle entry in haploid cell

Genes:

Genotypes:

FYPO:0002336 - normal chromatin silencing at silent mating-type cassette

Genes:

Genotypes:

FYPO:0005865 - normal histone H3-K9 methylation at silent mating-type cassette during vegetative growth

Genes:

Genotypes:

Single locus phenotype

FYPO:0007376 - abolished epigenetic heterochromatin inheritance

Genes:

Genotypes:

FYPO:0003074 - abolished protein localization to pericentric heterochromatin during vegetative growth

Genes:

Genotypes:

FYPO:0002827 - decreased chromatin silencing at silent mating-type cassette

Genes:

Genotypes:

FYPO:0000877 - decreased histone H3-K9 dimethylation at centromere during vegetative growth

Genes:

Genotypes:

FYPO:0002355 - decreased histone H3-K9 dimethylation at silent mating-type cassette during vegetative growth

Genes:

Genotypes:

FYPO:0004137 - decreased histone H3-K9 dimethylation at subtelomeric heterochromatin during vegetative growth

Genes:

Genotypes:

FYPO:0005845 - decreased histone H3-K9 trimethylation at silent mating-type cassette during vegetative growth

Genes:

Genotypes:

FYPO:0006670 - meiotic cell cycle entry in haploid cell

Genes:

Genotypes:

FYPO:0002336 - normal chromatin silencing at silent mating-type cassette

Genes:

Genotypes:

FYPO:0007278 - normal protein localization to euchromatin

Genes:

Genotypes: