Temporospatial coordination of meiotic DNA replication and recombination via DDK recruitment to replisomes.

Abstract:

:It has been long appreciated that, during meiosis, DNA replication is coordinated with the subsequent formation of the double-strand breaks (DSBs) that initiate recombination, but a mechanistic understanding of this process was elusive. We now show that, in yeast, the replisome-associated components Tof1 and Csm3 physically associate with the Dbf4-dependent Cdc7 kinase (DDK) and recruit it to the replisome, where it phosphorylates the DSB-promoting factor Mer2 in the wake of the replication fork, synchronizing replication with an early prerequisite for DSB formation. Recruiting regulatory kinases to replisomes may be a general mechanism to ensure spatial and temporal coordination of replication with other chromosomal processes.

journal_name

Cell

journal_title

Cell

authors

Murakami H,Keeney S

doi

10.1016/j.cell.2014.06.028

subject

Has Abstract

pub_date

2014-08-14 00:00:00

pages

861-873

issue

4

eissn

0092-8674

issn

1097-4172

pii

S0092-8674(14)00819-8

journal_volume

158

pub_type

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