A 105-KDA PROTEIN IS REQUIRED FOR YEAST MITOCHONDRIAL RNASE-P ACTIVITY

被引:78
作者
MORALES, MJ [1 ]
DANG, YL [1 ]
LOU, YC [1 ]
SULO, P [1 ]
MARTIN, NC [1 ]
机构
[1] UNIV LOUISVILLE, DEPT BIOCHEM, LOUISVILLE, KY 40292 USA
关键词
D O I
10.1073/pnas.89.20.9875
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
RNase P from the mitochondria of Saccharomyces cerevisiae was purified to near homogeneity >1800-fold with a yield of 1.6% from mitochondrial extracts. The most abundant protein in the purified fractions is, at 105 kDa, considerably larger than the 14-kDa bacterial RNase P protein subunits. Oligonucleotides designed from the amino-terminal sequence of the 105-kDa protein were used to identify and isolate the 105-kDa protein-encoding gene. Strains carrying a disruption of the gene for the 105-kDa protein are viable but respiratory deficient and accumulate mitochondrial tRNA precursors with 5' extensions. As this is the second gene known to be necessary for yeast mitochondrial RNase P activity, we have named it RPM2 (for RNase P mitochondrial).
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页码:9875 / 9879
页数:5
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