Hsieh Edward J, Dinoso Jason B, Clarke Catherine F
Department of Chemistry and Biochemistry and the Molecular Biology Institute, University of California, Los Angeles, CA 90095, USA.
Biochem Biophys Res Commun. 2004 Apr 30;317(2):648-53. doi: 10.1016/j.bbrc.2004.03.096.
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 bc1 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.
酿酒酵母基因ABC1最初是作为一个多拷贝抑制子被分离出来的,该抑制子存在于一个细胞色素b翻译激活因子(cbs2-223)发生突变的酵母菌株中。基于这一鉴定结果,推测Abc1p可激活bc1复合体并作为细胞色素b的伴侣蛋白发挥作用。ABC1随后被鉴定为COQ8,并发现它是酵母辅酶Q合成所必需的。在本研究中,我们发现一段包含ABC1/COQ8及相邻基因的酵母基因组DNA可抑制coq6突变体coq6-1的呼吸缺陷和Q缺陷表型。COQ6对酵母辅酶Q生物合成至关重要。我们发现位于ABC1/COQ8下游的一个tRNA(TRP)基因介导了对cbs2-223和coq6-1突变的抑制,并且在此处鉴定出这两个基因均含有UGA无义密码子。ABC1/COQ8无法以多拷贝形式抑制cbs2-223等位基因,这表明它可能并非如先前报道的那样是一种伴侣蛋白。