Temporal changes in Hec1 phosphorylation control kinetochore-microtubule attachment stability during mitosis.

ABSTRACT: Precise control of the attachment strength between kinetochores and spindle microtubules is essential to preserve genomic stability. Aurora B kinase has been implicated in regulating the stability of kinetochore-microtubule attachments but its relevant kinetochore targets in cells remain unclear. Here, we identify multiple serine residues within the N-terminus of the kinetochore protein Hec1 that are phosphorylated in an Aurora-B-kinase-dependent manner during mitosis. On all identified target sites, Hec1 phosphorylation at kinetochores is high in early mitosis and decreases significantly as chromosomes bi-orient. Furthermore, once dephosphorylated, Hec1 is not highly rephosphorylated in response to loss of kinetochore-microtubule attachment or tension. We find that a subpopulation of Auro

SUBMITTER: DeLuca KF 

PROVIDER: S-EPMC3031373 | biostudies-literature | 2011 Feb

REPOSITORIES: biostudies-literature