A mechanism for preventing asymmetric histone segregation onto replicating DNA strands

Chuanhe Yu, Haiyun Gan, Albert Serra-Cardona, Lin Zhang, Songlin Gan, Sushma Sharma, Erik Johansson, Andrei Chabes, Rui Ming Xu, Zhiguo Zhang

Research output: Contribution to journalArticlepeer-review

157 Scopus citations

Abstract

How parental histone (H3-H4)2 tetramers, the primary carriers of epigenetic modifications, are transferred onto leading and lagging strands of DNA replication forks for epigenetic inheritance remains elusive. Here we show that parental (H3-H4)2 tetramers are assembled into nucleosomes onto both leading and lagging strands, with a slight preference for lagging strands. The lagging-strand preference increases markedly in budding yeast cells lacking Dpb3 and Dpb4, two subunits of the leading strand DNA polymerase, Pol e, owing to the impairment of parental (H3-H4)2 transfer to leading strands. Dpb3-Dpb4 binds H3-H4 in vitro and participates in the inheritance of heterochromatin. These results indicate that different proteins facilitate the transfer of parental (H3-H4)2 onto leading versus lagging strands and that Dbp3-Dpb4 plays an important role in this poorly understood process.

Original languageEnglish (US)
Pages (from-to)1386-1389
Number of pages4
JournalScience
Volume361
Issue number6409
DOIs
StatePublished - Sep 28 2018
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2018 American Association for the Advancement of Science. All rights reserved.

Fingerprint

Dive into the research topics of 'A mechanism for preventing asymmetric histone segregation onto replicating DNA strands'. Together they form a unique fingerprint.

Cite this