Phosphorylation and Activation of 13S Condensin by Cdc2 in Vitro

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Abstract

13S condensin is a multisubunit protein complex essential for mitotic chromosome condensation in Xenopus egg extracts.Purified 13S condensin introduces positive supercoils into DNA in the presence of topoisomerase I and adenosine triphosphate in vitro. The supercoiling activity of 13S condensin was regulated by mitosis-specific phosphorylation. Immunodepletion, in vitro phosphorylation, and peptide-mapping experiments indicated that Cdc2 is likely to be the kinase that phosphorylates and activates 13S condensin. Multiple Cdc2 phosphorylation sites are clustered in the carboxyl-terminal domain of the XCAP-D2 (Xenopus chromosome-associated polypeptide D2) subunit. These results suggest that phosphorylation of 13S condensin by Cdc2 may trigger mitotic chromosome condensation in vitro.

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