RNase mitochondrial RNA processing correctly cleaves a novel R loop at the mitochondrial DNA leading-strand origin of replication

被引:64
|
作者
Lee, DY [1 ]
Clayton, DA [1 ]
机构
[1] STANFORD UNIV, SCH MED, BECKMAN CTR MOL & GENET MED, DEPT DEV BIOL, STANFORD, CA 94305 USA
关键词
replication priming; mitochondrial RNA processing; R loop; RNA-DNA hybrid; RNase MRP;
D O I
10.1101/gad.11.5.582
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The precursor primer RNA for mammalian mitochondrial DNA leading-strand replication remains as a persistent R loop formed during transcription through the mitochondrial DNA control region. We have examined model R loops, which exist in a novel and physiologically accurate preprimer conformation, as potential substrates for mammalian RNase mitochondrial RNA processing (MRP). Mouse RNase MRP accurately cleaves an R loop containing the mouse mitochondrial DNA origin. The multiple cleavage sites on the R-loop substrate match the priming sites observed in vivo, suggesting that RNase MRP alone is capable of generating virtually all of the leading-strand replication primers.
引用
收藏
页码:582 / 592
页数:11
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