Aurora A-dependent CENP-A phosphorylation at inner centromeres protects bioriented chromosomes against cohesion fatigue
Grégory Eot-Houllier (),
Laura Magnaghi-Jaulin,
Géraldine Fulcrand,
François-Xavier Moyroud,
Solange Monier and
Christian Jaulin ()
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Grégory Eot-Houllier: Université Rennes 1
Laura Magnaghi-Jaulin: Université Rennes 1
Géraldine Fulcrand: Université Rennes 1
François-Xavier Moyroud: Université Rennes 1
Solange Monier: Université Rennes 1
Christian Jaulin: Université Rennes 1
Nature Communications, 2018, vol. 9, issue 1, 1-13
Abstract:
Abstract Sustained spindle tension applied to sister centromeres during mitosis eventually leads to uncoordinated loss of sister chromatid cohesion, a phenomenon known as “cohesion fatigue.” We report that Aurora A-dependent phosphorylation of serine 7 of the centromere histone variant CENP-A (p-CENP-AS7) protects bioriented chromosomes against cohesion fatigue. Expression of a non-phosphorylatable version of CENP-A (CENP-AS7A) weakens sister chromatid cohesion only when sister centromeres are under tension, providing the first evidence of a regulated mechanism involved in protection against passive cohesion loss. Consistent with this observation, p-CENP-AS7 is detected at the inner centromere where it forms a discrete domain. The depletion or inhibition of Aurora A phenocopies the expression of CENP-AS7A and we show that Aurora A is recruited to centromeres in a Bub1-dependent manner. We propose that Aurora A-dependent phosphorylation of CENP-A at the inner centromere protects chromosomes against tension-induced cohesion fatigue until the last kinetochore is attached to spindle microtubules.
Date: 2018
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04089-9
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DOI: 10.1038/s41467-018-04089-9
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