Human DNA2 Is a Mitochondrial Nuclease/Helicase for Efficient Processing of DNA Replication and Repair Intermediates

被引:182
作者
Zheng, Li [1 ,2 ]
Zhou, Mian [1 ,2 ]
Guo, Zhigang [1 ,2 ]
Lu, Huiming [1 ,2 ]
Qian, Limin [1 ,2 ]
Dai, Huifang [1 ,2 ]
Qiu, Junzhuan [1 ,2 ]
Yakubovskaya, Elena [3 ]
Bogenhagen, Daniel F. [3 ]
Demple, Bruce [4 ]
Shen, Binghui [1 ,2 ]
机构
[1] City Hope Natl Med Ctr, Dept Radiat Biol, Duarte, CA 91010 USA
[2] Beckman Res Inst, Duarte, CA 91010 USA
[3] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
[4] Harvard Univ, Sch Med, Dept Genet & Complex Dis, Boston, MA 02115 USA
关键词
D O I
10.1016/j.molcel.2008.09.024
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
DNA2, a helicase/nuclease family member, plays versatile roles in processing DNA intermediates during DNA replication and repair. Yeast Dna2 (yDna2) is essential in RNA primer removal during nuclear DNA replication and is important in repairing UV damage, base damage, and double-strand breaks. Our data demonstrate that, surprisingly, human DNA2 (hDNA2) does not localize to nuclei, as it lacks a nuclear localization signal equivalent to that present in yDna2. Instead, hDNA2 migrates to the mitochondria, interacts with mitochondrial DNA polymerase gamma, and significantly stimulates polymerase activity. We further demonstrate that hDNA2 and flap endonuclease 1 synergistically process intermediate 5' flap structures occurring in DNA replication and long-patch base excision repair (LP-BER) in mitochondria. Depletion of hDNA2 from a mitochondrial extract reduces its efficiency in RNA primer removal and LP-BER. Taken together, our studies illustrate an evolutionarily diversified role of hDNA2 in mitochondrial DNA replication and repair in a mammalian system.
引用
收藏
页码:325 / 336
页数:12
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