Hsk1-Dfp1 is required for heterochromatin-mediated cohesion at centromeres

Heterochromatin performs a central role in chromosome segregation and stability by promoting cohesion at centromeres(1,2). Establishment of both heterochromatin-mediated silencing and cohesion requires passage through S phase, although the mechanism is unknown(3,4). Here we demonstrate that Schizosaccharomyces pombe Hsk1 (CDC7), a conserved Dbf4-dependent protein kinase (DDK) that regulates replication initiation(5), interacts with and phosphorylates the heterochromatin protein 1 (HP1) equivalent Swi6 (ref. 6). Hsk1 and its regulatory subunit Dfp1 function downstream of Swi6 localization to promote heterochromatin function and cohesion specifically at centromeres. This role for Hsk1-Dfp1 is separable from its replication initiation activity, providing a temporal link between S phase and centromere cohesion that is mediated by heterochromatin.