Synaptonemal complex protein SYCP3 impairs mitotic recombination by interfering with BRCA2

被引:37
|
作者
Hosoya, Noriko [1 ]
Okajima, Miyuki [1 ]
Kinomura, Aiko [2 ,3 ]
Fujii, Yoshihiro [1 ]
Hiyama, Takashi [2 ,4 ]
Sun, Jiying [3 ]
Tashiro, Satoshi [3 ]
Miyagawa, Kiyoshi [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Ctr Dis Biol & Integrat Med, Lab Mol Radiol, Tokyo 1130033, Japan
[2] Hiroshima Univ, Dept Human Genet, Hiroshima 7348553, Japan
[3] Hiroshima Univ, Res Inst Radiat Biol & Med, Dept Cellular Biol, Hiroshima 7348553, Japan
[4] Hiroshima Univ, Grad Sch Biomed Sci, Dept Surg, Hiroshima 7348553, Japan
基金
日本学术振兴会;
关键词
chromosomal instability; homologous recombination; meiosis-specific protein; FOCUS FORMATION; REPAIR; RAD51; CELLS; INHIBITION; TUMORS;
D O I
10.1038/embor.2011.221
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
The meiosis-specific synaptonemal complex protein SYCP3 has been reported to be aberrantly expressed in tumours. However, in contrast to its well-defined function in meiosis, its possible role in mitotic cells is entirely unknown. Here, we show that SYCP3 is expressed in a range of primary tumours and that it impairs chromosomal integrity in mitotic cells. Expression of SYCP3 inhibits the homologous recombination (HR) pathway mediated by RAD51, inducing hypersensitivity to DNA-damaging agents such as a poly(ADP-ribose) polymerase (PARP) inhibitor and chromosomal instability. SYCP3 forms a complex with BRCA2 and inhibits its role in HR. These findings highlight a new mechanism for chromosomal instability in cancer and extend the range of PARP-inhibitor sensitive tumours to those expressing SYCP3.
引用
收藏
页码:44 / 51
页数:8
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