Conserved sequence box II directs transcription termination and primer formation in mitochondriaw2

被引:102
作者
Pham, Xuan Hoi [1 ]
Farge, Geraldine [1 ]
Shi, Yonghong [1 ]
Gaspari, Martina [1 ]
Gustafsson, Claes M. [1 ]
Falkenberg, Maria [1 ]
机构
[1] Novum, Karolinska Inst, Div Metab Dis, Dept Lab Med, SE-14186 Stockholm, Sweden
关键词
BACTERIOPHAGE-T7; DEOXYRIBONUCLEIC-ACID; DNA-REPLICATION; MAMMALIAN-CELLS; RNASE-H; PURIFIED PROTEINS; PRIMARY ORIGIN; HUMAN MTDNA; IN-VITRO; POLYMERASE; INITIATION;
D O I
10.1074/jbc.M602429200
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 human mitochondrial transcription machinery generates the RNA primers needed for initiation of heavy strand DNA synthesis. Most DNA replication events from the heavy strand origin are prematurely terminated, forming a persistent RNA-DNA hybrid, which remains annealed to the parental DNA strand. This triple-stranded structure is called the D-loop and encompasses the conserved sequence box II, a DNA element required for proper primer formation. We here use a purified recombinant mitochondrial transcription system and demonstrate that conserved sequence box II is a sequence-dependent transcription termination element in vitro. Transcription from the light strand promoter is prematurely terminated at positions 300-282 in the mitochondrial genome, which coincide with the major RNA-DNA transition points in the D-loop of human mitochondria. Based on our findings, we propose a model for primer formation at the origin of heavy strand DNA replication.
引用
收藏
页码:24647 / 24652
页数:6
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