Repression of CENP-A assembly in metaphase requires HJURP phosphorylation and inhibition by M18BP1

Abstract

Centromeres are the foundation for mitotic kinetochore assembly and thus are essential for chromosome segregation. Centromeres are epigenetically defined by nucleosomes containing the histone H3 variant CENP-A. CENP-A nucleosome assembly is uncoupled from replication and occurs in G1 but how cells control this timing is incompletely understood. The formation of CENP-A nucleosomes in vertebrates requires CENP-C and the Mis18 complex which recruit the CENP-A chaperone HJURP to centromeres. Using a cell-free system for centromere assembly in X. laevis egg extracts, we discover two activities that inhibit CENP-A assembly in metaphase. HJURP phosphorylation prevents the interaction between HJURP and CENP-C in metaphase, blocking the delivery of soluble CENP-A to centromeres. Non-phosphorylatable mutants of HJURP constitutively bind CENP-C in metaphase but are not sufficient for new CENP-A assembly. We find that the M18BP1.S subunit of the Mis18 complex also binds to CENP-C to competitively inhibit HJURPs access to centromeres. Removal of these two inhibitory activities causes CENP-A assembly in metaphase. SUMMARYVertebrate CENP-A assembly is normally restricted to G1 phase. Two inhibitory activities, phosphorylation of HJURP and competitive binding of M18BP1.S to CENP-C, block HJURPs access to the metaphase centromere. Removal of these inhibitory activities causes CENP-A assembly in metaphase.