Beckmann J D, Ljungdahl P O, Lopez J L, Trumpower B L
J Biol Chem. 1987 Jun 25;262(18):8901-9.
The nuclear gene encoding the Rieske iron-sulfur protein of the cytochrome bc1 complex of the mitochondrial respiratory chain has been isolated and characterized from Saccharomyces cerevisiae. We used a segment of the iron-sulfur protein gene from Neurospora crassa (Harnisch, U., Weiss, H., and Sebald, W. (1985) Eur. J. Biochem. 149, 95-99) to detect the yeast gene by Southern analysis. Five different but overlapping clones were then isolated by probing a yeast genomic library carried on YEp 13 by colony lift hybridization. Several approaches confirmed that the isolated DNA contained the gene for the Rieske iron-sulfur protein. The yeast gene, which contains no introns, can be expressed in Escherichia coli. A 900-base pair HindIII-EcoRI fragment was subcloned into pUC19 and directed the synthesis of immunodetectable protein. The gene was also identified by disruption of its chromosomal copy by homologous integration. A 400 base pair PstI-EcoRI fragment cloned adjacent to a HIS3 marker in pUC18 was used as an integrating vector. HIS+ transformants were obtained which were unable to grow on the nonfermentable carbon source glycerol. Southern analysis of the respiration deficient (gly-) strains confirmed that the chromosomal copy of the gene was disrupted, and immunoblots of extracts of the transformants indicated a lack of iron-sulfur protein. A respiration-deficient integrant was transformed to GLY+ by a 2-kilobase pair HindIII-BglII fragment, including a complete copy of the gene, carried on a multicopy episomal vector. Immunoblots with monoclonal antibodies to the iron-sulfur protein indicated overproduction of the protein in the complemented strain and revealed expression of approximately equal amounts of mature iron-sulfur protein and of a protein approximately 3 kDa larger than the mature protein in the complemented strain. A 1.2-kilobase pair segment of DNA from the clone which complemented the disrupted strains was sequenced and found to contain an open reading frame of 645 nucleotides, capable of encoding a 21,946-dalton protein. The gene is flanked by consensus signal sequences for initiation and termination which are common in yeast and is preceded by a possible upstream activating sequence. Amino acid sequence analysis of the amino-terminal end of the mature iron-sulfur protein agreed exactly with that predicted by the nucleotide sequence starting at Lys-31.(ABSTRACT TRUNCATED AT 400 WORDS)
编码线粒体呼吸链细胞色素bc1复合物中铁硫蛋白的核基因已从酿酒酵母中分离并鉴定。我们用来自粗糙脉孢菌的铁硫蛋白基因片段(哈尼斯奇,U.,魏斯,H.,和泽巴尔德,W.(1985年)欧洲生物化学杂志149卷,95 - 99页)通过Southern印迹分析来检测酵母基因。然后通过菌落杂交筛选携带在YEp 13上的酵母基因组文库,分离出五个不同但重叠的克隆。几种方法证实分离得到的DNA含有铁硫蛋白基因。该酵母基因不含内含子,能在大肠杆菌中表达。一个900碱基对的HindIII - EcoRI片段被亚克隆到pUC19中,并指导合成可免疫检测的蛋白。该基因也通过同源整合破坏其染色体拷贝而被鉴定。一个克隆在pUC18中与HIS3标记相邻的400碱基对的PstI - EcoRI片段被用作整合载体。获得了在非发酵碳源甘油上不能生长的HIS +转化体。对呼吸缺陷(gly -)菌株的Southern印迹分析证实该基因的染色体拷贝被破坏,对转化体提取物的免疫印迹表明缺乏铁硫蛋白。一个呼吸缺陷整合体被一个包含该基因完整拷贝且携带在多拷贝附加型载体上的2千碱基对的HindIII - BglII片段转化为GLY +。用针对铁硫蛋白的单克隆抗体进行免疫印迹表明在互补菌株中该蛋白过量产生,并揭示在互补菌株中成熟铁硫蛋白和比成熟蛋白大约大3 kDa的一种蛋白表达量大致相等。对互补了破坏菌株的克隆中的一个1.2千碱基对的DNA片段进行测序,发现它含有一个645个核苷酸的开放阅读框,能够编码一个21,946道尔顿的蛋白。该基因两侧是酵母中常见的起始和终止共有信号序列,并且前面有一个可能的上游激活序列。对成熟铁硫蛋白氨基末端的氨基酸序列分析与从赖氨酸 - 31开始的核苷酸序列预测完全一致。(摘要截短至400字)