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Both DNA Polymerases δ and ε Contact Active and Stalled Replication Forks Differently.
Yu, Chuanhe; Gan, Haiyun; Zhang, Zhiguo.
Afiliação
  • Yu C; Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, USA.
  • Gan H; Institute for Cancer Genetics, Department of Pediatrics, and Department of Genetics and Development, Columbia University, Irving Cancer Research Center, New York, New York, USA.
  • Zhang Z; Institute for Cancer Genetics, Department of Pediatrics, and Department of Genetics and Development, Columbia University, Irving Cancer Research Center, New York, New York, USA zz2401@cumc.columbia.edu.
Mol Cell Biol ; 37(21)2017 Nov 01.
Article em En | MEDLINE | ID: mdl-28784720
ABSTRACT
Three DNA polymerases, polymerases α, δ, and ε (Pol α, Pol δ, and Pol ε), are responsible for eukaryotic genome duplication. When DNA replication stress is encountered, DNA synthesis stalls until the stress is ameliorated. However, it is not known whether there is a difference in the association of each polymerase with active and stalled replication forks. Here, we show that each DNA polymerase has a distinct pattern of association with active and stalled replication forks. Pol α is enriched at extending Okazaki fragments of active and stalled forks. In contrast, although Pol δ contacts the nascent lagging strands of active and stalled forks, it binds to only the matured (and not elongating) Okazaki fragments of stalled forks. Pol ε has greater contact with the nascent single-stranded DNA (ssDNA) of the leading strand on active forks than on stalled forks. We propose that the configuration of DNA polymerases at stalled forks facilitates the resumption of DNA synthesis after stress removal.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / DNA Fúngico / DNA Polimerase II / DNA Polimerase III Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / DNA Fúngico / DNA Polimerase II / DNA Polimerase III Idioma: En Ano de publicação: 2017 Tipo de documento: Article