A tRNATRP gene mediates the suppression of cbs2-223 previously attributed to ABC1/COQ8

被引:35
作者
Hsieh, EJ
Dinoso, JB
Clarke, CF [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
coenzyme Q; Ubiquinone; ABCl; COQ8; CBS2; mitochondria; respiration;
D O I
10.1016/j.bbrc.2004.03.096
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Saccharomyces cerevisiae gene ABC1 was originally isolated as a multicopy suppressor of a yeast strain harboring a mutation in a cytochrome b translational activator (cbs2-223). Based on this identification, Abc1p was postulated to activate the bc(1) complex and function as a chaperone of cytochrome b. ABC1 was subsequently identified as COQ8 and found to be necessary for yeast coenzyme Q synthesis. In this work we show that a segment of yeast genomic DNA containing ABC1\COQ8 and neighboring genes suppresses the respiratory and Q-deficient phenotypes of the coq6 mutant, coq6-1. COQ6 is essential for yeast coenzyme Q biosynthesis. We show that a tRNA(TRP) gene located downstream of ABC1\COQ8 mediates suppression of the cbs2-223 and coq6-1 mutations, and each is identified here as containing UGA nonsense codons. The inability of ABC1\COQ8 to suppress the cbs2-223 allele in multicopy indicates it may not be a chaperone as previously reported. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:648 / 653
页数:6
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