The astrin-kinastrin/SKAP complex localizes to microtubule plus ends and facilitates chromosome alignment.

Article Details

Citation

Dunsch AK, Linnane E, Barr FA, Gruneberg U

The astrin-kinastrin/SKAP complex localizes to microtubule plus ends and facilitates chromosome alignment.

J Cell Biol. 2011 Mar 21;192(6):959-68. doi: 10.1083/jcb.201008023. Epub 2011 Mar 14.

PubMed ID
21402792 [ View in PubMed
]
Abstract

Astrin is a mitotic spindle-associated protein required for the correct alignment of all chromosomes at the metaphase plate. Astrin depletion delays chromosome alignment and causes the loss of normal spindle architecture and sister chromatid cohesion before anaphase onset. Here we describe an astrin complex containing kinastrin/SKAP, a novel kinetochore and mitotic spindle protein, and three minor interaction partners: dynein light chain, Plk1, and Sgo2. Kinastrin is the major astrin-interacting protein in mitotic cells, and is required for astrin targeting to microtubule plus ends proximal to the plus tip tracking protein EB1. Cells overexpressing or depleted of kinastrin mislocalize astrin and show the same mitotic defects as astrin-depleted cells. Importantly, astrin fails to localize to and track microtubule plus ends in cells depleted of or overexpressing kinastrin. These findings suggest that microtubule plus end targeting of astrin is required for normal spindle architecture and chromosome alignment, and that perturbations of this pathway result in delayed mitosis and nonphysiological separase activation.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Serine/threonine-protein kinase PLK1P53350Details