Journal
MOLECULAR CELL
Volume 72, Issue 1, Pages 140-+Publisher
CELL PRESS
DOI: 10.1016/j.molcel.2018.09.001
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Funding
- NIH [R35GM118015]
- MRC [MC_UU_12016/13]
- Wellcome Trust [102943/Z/13/Z]
- Wellcome Trust [102943/Z/13/Z] Funding Source: Wellcome Trust
- MRC [MC_UU_00018/4, MC_UU_12016/13] Funding Source: UKRI
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Although essential for epigenetic inheritance, the transfer of parental histone (H3-H4)(2) tetramers that contain epigenetic modifications to replicating DNA strands is poorly understood. Here, we show that the Mcm2-Ctf4-Pol alpha axis facilitates the transfer of parental (H3-H4)(2) tetramers to lagging-strand DNA at replication forks. Mutating the conserved histone-binding domain of the Mcm2 subunit of the CMG (Cdc45-MCM-GINS) DNA helicase, which translocates along the leading-strand template, results in a marked enrichment of parental (H3-H4)(2) on leading strand, due to the impairment of the transfer of parental (H3-H4)(2) to lagging strands. Similar effects are observed in Ctf4 and Pol alpha primase mutants that disrupt the connection of the CMG helicase to Pol alpha that resides on lagging-strand template. Our results support a model whereby parental (H3-H4)(2) complexes displaced from nucleosomes by DNA unwinding at replication forks are transferred by the CMG-Ctf4-Pol alpha complex to lagging-strand DNA for nucleosome assembly at the original location.
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