Gadgil R, Barthelemy J, Lewis T, Leffak M
Department of Biochemistry and Molecular Biology, Boonshoft School of Medicine, Wright State University, Dayton, OH 45435, USA.
Department of Biochemistry and Molecular Biology, Boonshoft School of Medicine, Wright State University, Dayton, OH 45435, USA.
Biophys Chem. 2017 Jun;225:38-48. doi: 10.1016/j.bpc.2016.11.007. Epub 2016 Nov 22.
Microsatellites are short, tandemly repeated DNA motifs of 1-6 nucleotides, also termed simple sequence repeats (SRSs) or short tandem repeats (STRs). Collectively, these repeats comprise approximately 3% of the human genome Subramanian et al. (2003), Lander and Lander (2001) [1,2], and represent a large reservoir of loci highly prone to mutations Sun et al. (2012), Ellegren (2004) [3,4] that contribute to human evolution and disease. Microsatellites are known to stall and reverse replication forks in model systems Pelletier et al. (2003), Samadashwily et al. (1997), Kerrest et al. (2009) [5-7], and are hotspots of chromosomal double strand breaks (DSBs). We briefly review the relationship of these repeated sequences to replication stalling and genome instability, and present recent data on the impact of replication stress on DNA fragility at microsatellites in vivo.
微卫星是由1至6个核苷酸组成的短串联重复DNA基序,也被称为简单序列重复(SSRs)或短串联重复序列(STRs)。这些重复序列共同构成了人类基因组的约3% (Subramanian等人,2003年;Lander和Lander,2001年 [1,2]),代表了一个极易发生突变的基因座库(Sun等人,2012年;Ellegren,2004年 [3,4]),这些突变对人类进化和疾病产生影响。已知微卫星在模型系统中会使复制叉停滞并逆转(Pelletier等人,2003年;Samadashwily等人,1997年;Kerrest等人,2009年 [5-7]),并且是染色体双链断裂(DSBs)的热点区域。我们简要回顾这些重复序列与复制停滞和基因组不稳定性之间的关系,并展示关于体内复制应激对微卫星处DNA脆性影响的最新数据。