| Literature DB >> 30244834 |
Haiyun Gan1, Albert Serra-Cardona1, Xu Hua1, Hui Zhou1, Karim Labib2, Chuanhe Yu3, Zhiguo Zhang4.
Abstract
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-Polα 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 Polα primase mutants that disrupt the connection of the CMG helicase to Polα 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-Polα complex to lagging-strand DNA for nucleosome assembly at the original location.Entities:
Keywords: Ctf4; DNA replication; Mcm2; Pol1; epigenetic inheritance; histone modifications; nucleosome assembly; parental histone transfer
Mesh:
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Year: 2018 PMID: 30244834 PMCID: PMC6193272 DOI: 10.1016/j.molcel.2018.09.001
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970