DNA-dependent protein kinase defects are linked to deficiencies in DNA repair and V(D)J recombination

被引:33
作者
Finnie, NJ
Gottlieb, TM
Blunt, T
Jeggo, PA
Jackson, SP
机构
[1] WELLCOME CRC INST,CAMBRIDGE CB2 1QR,ENGLAND
[2] UNIV CAMBRIDGE,DEPT ZOOL,CAMBRIDGE,ENGLAND
[3] UNIV SUSSEX,MRC,CELL MUTAT UNIT,BRIGHTON BN1 9RR,E SUSSEX,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1098/rstb.1996.0014
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA-dependent protein kinase is a nuclear serine/threonine kinase whose catalytic properties are expressed only when the enzyme is bound to DNA ends or other discontinuities in the DNA. DNA-PK comprises two components: one mediates binding to DNA and corresponds to the heterodimeric human autoimmune antigen Ku; the other, DNA-PK catalytic subunit (DNA-PKes), is a polypeptide of approximately 450 kDa. DNA-PR deficiencies are associated with certain mutant rodent cell lines that display defects in DNA double strand break repair and V(D)J recombination. Specifically, hamster xrs-6 cells lack Ku function, whereas murine scid and hamster V3 cells lack functional DNA-PKes. Furthermore, the phenotypes of xrs-6 and V3 cells can be corrected by the expression of the genes encoding the 80 kDa component of Ku or DNA-PKes, respectively. These results imply that DNA-PK is an important component of the DNA double strand break repair/recombination apparatus. Possible roles for DNA-PK in these processes are discussed.
引用
收藏
页码:173 / 179
页数:7
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