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Reference - PMID:25579976 - Phosphorylation of cohesin Rec11/SA3 by casein kinase 1 promotes homologous recombination by assembling the meiotic chromosome axis.

Reference summary

PubMed ID
PMID:25579976
Title
Phosphorylation of cohesin Rec11/SA3 by casein kinase 1 promotes homologous recombination by assembling the meiotic chromosome axis.
Authors
Sakuno T, Watanabe Y
Citation
Dev Cell 2015 Jan 26;32(2):220-30
Publication year
2015
Abstract
In meiosis, cohesin is required for sister chromatid cohesion, as well as meiotic chromosome axis assembly and recombination. However, mechanisms underlying the multifunctional nature of cohesin remain elusive. Here, we show that fission yeast casein kinase 1 (CK1) plays a crucial role in assembling the meiotic chromosome axis (so-called linear element: LinE) and promoting recombination. An in vitro phosphorylation screening assay identified meiotic cohesin subunit Rec11/SA3 as an excellent substrate of CK1. The phosphorylation of Rec11 by CK1 mediates the interaction with the Rec10/Red1/SCP2 axis component, a key step in meiotic chromosome axis assembly, and is dispensable for sister chromatid cohesion. Crucially, the expression of Rec11-Rec10 fusion protein nearly completely bypasses the requirement for CK1 or cohesin phosphorylation for LinE assembly and recombination. This study uncovers a central mechanism of the cohesin-dependent assembly of the meiotic chromosome axis and recombination apparatus that acts independently of sister chromatid cohesion.

Annotation

GO biological process

GO:0030999 - linear element assembly

Genes:

GO:0090006 - regulation of linear element assembly

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GO cellular component

GO:0000785 - chromatin

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GO:0005634 - nucleus

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GO molecular function

GO:0005515 - protein binding

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GO:0004674 - protein serine/threonine kinase activity

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Modification

MOD:00046 - O-phospho-L-serine

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MOD:00696 - phosphorylated residue

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Multi-locus phenotype

FYPO:0003564 - abnormal meiotic DNA double-strand break formation

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Genotypes:

FYPO:0002957 - abnormal protein localization to nucleus during meiosis

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Genotypes:

FYPO:0002485 - decreased intergenic meiotic recombination

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Genotypes:

FYPO:0002219 - normal chromosome disjunction at meiosis I

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Genotypes:

FYPO:0004667 - normal meiotic sister chromatid cohesion at centromere

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Genotypes:

FYPO:0005634 - sister kinetochore dissociation in meiotic metaphase I with equational sister chromatid segregation in meiosis I

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Single locus phenotype

FYPO:0000197 - abnormal horsetail movement

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Genotypes:

FYPO:0002890 - abnormal horsetail nucleus morphology

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Genotypes:

FYPO:0004585 - abnormal linear element morphology

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Genotypes:

FYPO:0003564 - abnormal meiotic DNA double-strand break formation

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Genotypes:

FYPO:0000705 - abolished protein-protein interaction

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Genotypes:

FYPO:0002485 - decreased intergenic meiotic recombination

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Genotypes:

FYPO:0003615 - decreased meiotic DNA double-strand break formation

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Genotypes:

FYPO:0002093 - decreased meiotic sister chromatid cohesion

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Genotypes:

FYPO:0006423 - decreased meiotic sister chromatid cohesion at centromere during meiosis I

Genes:

Genotypes:

FYPO:0005576 - decreased protein localization to chromatin during meiotic cell cycle

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Genotypes:

FYPO:0005577 - decreased protein phosphorylation during meiotic cell cycle

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Genotypes:

FYPO:0002219 - normal chromosome disjunction at meiosis I

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Genotypes:

FYPO:0003835 - normal horsetail movement

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FYPO:0003562 - normal horsetail nucleus morphology

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Genotypes:

FYPO:0005578 - normal intergenic meiotic recombination

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Genotypes:

FYPO:0003891 - normal intragenic meiotic recombination

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Genotypes:

FYPO:0004667 - normal meiotic sister chromatid cohesion at centromere

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Genotypes: