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The PCNA-Pol δ complex couples lagging strand DNA synthesis to parental histone transfer for epigenetic inheritance.
Serra-Cardona, Albert; Hua, Xu; McNutt, Seth W; Zhou, Hui; Toda, Takenori; Jia, Songtao; Chu, Feixia; Zhang, Zhiguo.
Afiliación
  • Serra-Cardona A; Institute for Cancer Genetics, Department of Pediatrics and Department of Genetics and Development, Columbia University Irving Medical Center, New York, NY 10019, USA.
  • Hua X; Institute for Cancer Genetics, Department of Pediatrics and Department of Genetics and Development, Columbia University Irving Medical Center, New York, NY 10019, USA.
  • McNutt SW; Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH 03824, USA.
  • Zhou H; Institute for Cancer Genetics, Department of Pediatrics and Department of Genetics and Development, Columbia University Irving Medical Center, New York, NY 10019, USA.
  • Toda T; Department of Biological Sciences, Columbia University, New York, NY 10027, USA.
  • Jia S; Department of Biological Sciences, Columbia University, New York, NY 10027, USA.
  • Chu F; Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH 03824, USA.
  • Zhang Z; Institute for Cancer Genetics, Department of Pediatrics and Department of Genetics and Development, Columbia University Irving Medical Center, New York, NY 10019, USA.
Sci Adv ; 10(23): eadn5175, 2024 Jun 07.
Article en En | MEDLINE | ID: mdl-38838138
ABSTRACT
Inheritance of epigenetic information is critical for maintaining cell identity. The transfer of parental histone H3-H4 tetramers, the primary carrier of epigenetic modifications on histone proteins, represents a crucial yet poorly understood step in the inheritance of epigenetic information. Here, we show the lagging strand DNA polymerase, Pol δ, interacts directly with H3-H4 and that the interaction between Pol δ and the sliding clamp PCNA regulates parental histone transfer to lagging strands, most likely independent of their roles in DNA synthesis. When combined, mutations at Pol δ and Mcm2 that compromise parental histone transfer result in a greater reduction in nucleosome occupancy at nascent chromatin than mutations in either alone. Last, PCNA contributes to nucleosome positioning on nascent chromatin. On the basis of these results, we suggest that the PCNA-Pol δ complex couples lagging strand DNA synthesis to parental H3-H4 transfer, facilitating epigenetic inheritance.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Histonas / Antígeno Nuclear de Célula en Proliferación / Epigénesis Genética / ADN Polimerasa III / Replicación del ADN Límite: Humans Idioma: En Revista: Sci Adv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Histonas / Antígeno Nuclear de Célula en Proliferación / Epigénesis Genética / ADN Polimerasa III / Replicación del ADN Límite: Humans Idioma: En Revista: Sci Adv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos