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Migrating bubble synthesis promotes mutagenesis through lesions in its template
Authors:Beth Osia  Jerzy Twarowski  Tyler Jackson  Kirill Lobachev  Liping Liu  Anna Malkova
Affiliation:Department of Biology, University of Iowa, Iowa City, IA,  52245, USA;Department of Cancer Genetics and Epigenetics, City of Hope, Duarte, CA,  91010, USA;Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX,  77030, USA;School of Biological Sciences, Georgia Institute of Technology, Atlanta, GE,  30332, USA
Abstract:Break-induced replication (BIR) proceeds via a migrating D-loop for hundreds of kilobases and is highly mutagenic. Previous studies identified long single-stranded (ss) nascent DNA that accumulates during leading strand synthesis to be a target for DNA damage and a primary source of BIR-induced mutagenesis. Here, we describe a new important source of mutagenic ssDNA formed during BIR: the ssDNA template for leading strand BIR synthesis formed during D-loop migration. Specifically, we demonstrate that this D-loop bottom template strand (D-BTS) is susceptible to APOBEC3A (A3A)-induced DNA lesions leading to mutations associated with BIR. Also, we demonstrate that BIR-associated ssDNA promotes an additional type of genetic instability: replication slippage between microhomologies stimulated by inverted DNA repeats. Based on our results we propose that these events are stimulated by both known sources of ssDNA formed during BIR, nascent DNA formed by leading strand synthesis, and the D-BTS that we describe here. Together we report a new source of mutagenesis during BIR that may also be shared by other homologous recombination pathways driven by D-loop repair synthesis.
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