Novel functional requirements for non-homologous DNA end joining in Schizosaccharomyces pombe

被引:132
作者
Manolis, KG
Nimmo, ER
Hartsuiker, E
Carr, AM
Jeggo, PA [1 ]
Allshire, RC
机构
[1] Univ Sussex, MRC, Cell Mutat Unit, Brighton BN1 9RR, E Sussex, England
[2] Western Gen Hosp, Human Genet Unit, MRC, Canc Res Campaign Project, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
DNA ligase IV; Ku70; Mre11; silencing; telomere length;
D O I
10.1093/emboj/20.1.210
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA double strand break (DSB) repair by non-homologous end joining (NHEJ) in mammalian cells requires the Ku70-Ku80 heterodimer, the DNA-PK catalytic subunit DNA-PKcs, as well as DNA ligase IV and Xrcc4, NHEJ of plasmid DSBs in Saccharomyces cerevisiae requires Ku, Xrcc4 and DNA ligase IV, as well as Mre11, Rad50, Xrs2 and DNA damage checkpoint proteins. Saccharomyces cerevisiae Ku is also required for telomere length maintenance and transcriptional silencing, We have characterized NHEJ in Schizosaccharomyces pombe using an extrachromosomal assay and find that, as anticipated, it is Ku70 and DNA ligase IV dependent. Unexpectedly, we find that Rad32, Rad50 (the S.pombe homologues of Mre11 and Rad50, respectively) and checkpoint proteins are not required for NHEJ. Furthermore, although S.pombe Ku70 is required for maintenance of telomere length, it is dispensable for transcriptional silencing at telomeres and is located throughout the nucleus rather than concentrated at the telomeres, Together, these results provide insight into the mechanism of NHEJ and contrast significantly with recent studies in S. cerevisiae.
引用
收藏
页码:210 / 221
页数:12
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