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.
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UNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94143 USA
CHA, TA
ALBERTS, BM
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UNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94143 USA
机构:
Univ Gothenburg, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, Sweden
Karolinska Inst, Div Metab Dis, SE-14186 Stockholm, SwedenUniv Gothenburg, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, Sweden
Wanrooij, Paulina H.
Uhler, Jay P.
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Univ Gothenburg, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, SwedenUniv Gothenburg, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, Sweden
Uhler, Jay P.
Shi, Yonghong
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Univ Gothenburg, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, Sweden
Karolinska Inst, Div Metab Dis, SE-14186 Stockholm, SwedenUniv Gothenburg, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, Sweden