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The ATR-Activation Domain of TopBP1 Is Required for the Suppression of Origin Firing during the S Phase.
Sokka, Miiko; Koalick, Dennis; Hemmerich, Peter; Syväoja, Juhani E; Pospiech, Helmut.
Afiliação
  • Sokka M; Department of Biology, University of Eastern Finland, FI-80101 Joensuu, Finland. miiko_sokka@brown.edu.
  • Koalick D; Institute of Biomedicine, University of Eastern Finland, FI-70211 Kuopio, Finland. miiko_sokka@brown.edu.
  • Hemmerich P; Leibniz Institute on Aging-Fritz Lipmann Institute, DE-07745 Jena, Germany. dennis.koalick@yahoo.com.
  • Syväoja JE; Leibniz Institute on Aging-Fritz Lipmann Institute, DE-07745 Jena, Germany. peter.hemmerich@leibniz-fli.de.
  • Pospiech H; Institute of Biomedicine, University of Eastern Finland, FI-70211 Kuopio, Finland. juhani.syvaoja@live.com.
Int J Mol Sci ; 19(8)2018 Aug 13.
Article em En | MEDLINE | ID: mdl-30104465
The mammalian DNA replication program is controlled at two phases, the licensing of potential origins of DNA replication in early gap 1 (G1), and the selective firing of a subset of licenced origins in the synthesis (S) phase. Upon entry into the S phase, serine/threonine-protein kinase ATR (ATR) is required for successful completion of the DNA replication program by limiting unnecessary dormant origin activation. Equally important is its activator, DNA topoisomerase 2-binding protein 1 (TopBP1), which is also required for the initiation of DNA replication after a rise in S-phase kinase levels. However, it is unknown how the ATR activation domain of TopBP1 affects DNA replication dynamics. Using human cells conditionally expressing a TopBP1 mutant deficient for ATR activation, we show that functional TopBP1 is required in suppressing local dormant origin activation. Our results demonstrate a regulatory role for TopBP1 in the local balancing of replication fork firing within the S phase.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Proteínas de Transporte / Proteínas de Ligação a DNA Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Proteínas de Transporte / Proteínas de Ligação a DNA Idioma: En Ano de publicação: 2018 Tipo de documento: Article