期刊论文详细信息
FEBS Letters
ATP13, a nuclear gene of Saccharomyces cerevisiae essential for the expression of subunit 9 of the mitochondrial ATPase
Douglas, Michael G.1  Tzagoloff, Alexander2  Ackerman, Sharon H.2  Gellefors, Pär1  Gatti, Domenico L.2 
[1] Department of Biochemistry, University of North Carolina, Chapel Hill, NC 27599, USA;Department of Biological Sciences, Columbia University, New York, NY 10027, USA
关键词: Yeast;    Mitochondrion;    ATP13;    ATPase;    Subunit 9;    Translation;    pet mutant;    respiratory deficient mutant of yeast with a genetic lesion in a nuclear gene;    ϱ° mutant;    respiratory deficient mutant of yeast lacking mitochondrial DNA;    DBM;    diazobenyloxymethyl;    kb;    kilobase (pairs);    bp;    base pairs;   
DOI  :  10.1016/0014-5793(91)80124-L
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

The respiratory deficient nuclear mutant of Saccharomyces cerevisiae, N9-168, assigned to complementation group G95 was previously shown to lack subunit 9, one of the three mitochondrially encoded subunits of the F0 component of the mitochondrial ATPase. As a consequence of the structural defect in F0, the ATPase activity of G95 mutants is not inhibited by rutamycin. The absence of subunit 9 in N9-168 has been correlated with a lower steady-state level of its mRNA and an increase in higher molecular weight precursor transcripts. These results suggest that the mutation is most likely to affect either translation of the ??? mRNA or processing or the primary transcript. We have isolated a nuclear gene, designated ATP13, which complements the respiratory defect and restores rutamycin-sensitive ATPase in G95 mutants. Disruption of ATP13 induces a respiratory deficiency which is not complemented by G95 mutants. The nucleotide sequence of ATP13 indicates a primary translation product with an M??? of 42 897. The protein has a basic amino terminal signal sequence that is cleaved upon import into mitochondria. No significant primary structure homology is detected with any protein in the most recent libraries.

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