Multiple genes, including a member of the AAA family, are essential for degradation of unassembled subunit 2 of cytochrome c oxidase in yeast mitochondria
Multiple genes, including a member of the AAA family, are essential for degradation of unassembled subunit 2 of cytochrome c oxidase in yeast mitochondria
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多个基因,包括 AAA 家族的成员,对于酵母线粒体中细胞色素 c 氧化酶未组装的亚基 2 的降解至关重要
DOI:
--
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发表时间:
1995
影响因子:
5.3
通讯作者:
Andakira Ohashi
中科院分区:
文献类型:
--
作者:
Toshiki Nakai;T. Yasuhara;Yukio Fujiki;Andakira Ohashi
Cytochrome c oxidase consists of three mitochondrion- and several nucleus-encoded subunits. We previously found that in a mutant of Saccharomyces cerevisiae lacking nucleus-encoded subunit 4 of this enzyme (CoxIV), subunits 2 and 3 (CoxII and CoxIII), both encoded by the mitochondrial DNA, were unstable and rapidly degraded in mitochondria, presumably because the subunits cannot assemble normally. To analyze the molecular machinery involved in this proteolytic pathway, we obtained four mutants defective in the degradation of unassembled CoxII (osd mutants) by screening CoxIV-deficient cells for the accumulation of CoxII. All of the mutants were recessive and were classified into three different complementation groups. Tetrad analyses revealed that the phenotype of each mutant was caused by a single nuclear mutation. These results suggest strongly that at least three nuclear genes (the OSD genes) are required for this degradation system. Interestingly, degradation of CoxIII was not affected in the mutants, implying that the two subunits are degraded by distinct pathways. We also cloned the OSD1 gene by complementation of the temperature sensitivity of osd1-1 mutants with a COXIV+ genetic background on a nonfermentable glycerol medium. We found it to encode a member of a family (the AAA family) of putative ATPases, which proved to be identical to recently described YME1 and YTA11. Immunological analyses revealed that Osd1 protein is localized to the mitochondrial inner membrane. Disruption of the predicted ATP-binding cassette by site-directed mutagenesis eliminated biological activities, thereby underscoring the importance of ATP for function.
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DOI:
10.1016/s0021-9258(17)42340-4
发表时间:
1994-01
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
L. van Dyck;D. Pearce;F. Sherman
通讯作者:
L. van Dyck;D. Pearce;F. Sherman
DOI:
--
发表时间:
1985
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Watabe,S;Kimura,T
通讯作者:
Kimura,T
影响因子:
3.3
作者:
Thorsness,PE;Fox,TD
通讯作者:
Fox,TD
DOI:
10.1073/pnas.85.21.7852
发表时间:
1988-11-01
影响因子:
11.1
作者:
BLOCK, MR;GLICK, BS;ROTHMAN, JE
通讯作者:
ROTHMAN, JE
DOI:
--
发表时间:
1993
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Taanman,JW;Capaldi,RA
通讯作者:
Capaldi,RA