Glerum D M, Shtanko A, Tzagoloff A, Gorman N, Sinclair P R
Department of Biological Sciences, Columbia University, New York, NY 10027, USA.
Yeast. 1996 Nov;12(14):1421-5. doi: 10.1002/(SICI)1097-0061(199611)12:14%3C1421::AID-YEA38%3E3.0.CO;2-W.
A respiratory-defective mutant (C54) of Saccharomyces cerevisiae was found to have a phenotype consistent with a mutation in either mitochondrial protoporphyrinogen oxidase or ferrochelatase. The mutant is grossly deficient in hemes, accumulates protoporphyrin and is rescued by exogenous heme. The increased levels of protoporphyrin at the expense of heme is indicative of a block in one of the two last steps of the heme biosynthetic pathway. Complementation of C54 by a known ferrochelatase mutant suggested that the defect was most likely in HEM14 encoding protoporphyrinogen oxidase. A plasmid capable of complementing C54 was obtained by transformation with a yeast genomic plasmid library. A partial sequence of the insert identified the gene as reading frame YER014 of yeast chromosome V (GenBank Accession Number U18778). This reading frame codes for a protein homologous to human protoporphyrinogen oxidase. Disruption of this gene elicits a respiratory defect and accumulation of protoporphyrin. The phenotype of the null mutant together with the homology of YER014p to human protoporphyrinogen oxidase provide compelling evidence that YER014 is HEM14.
酿酒酵母的一个呼吸缺陷型突变体(C54)被发现具有与线粒体原卟啉原氧化酶或亚铁螯合酶突变相一致的表型。该突变体严重缺乏血红素,积累原卟啉,并且可被外源性血红素拯救。以血红素为代价的原卟啉水平升高表明血红素生物合成途径的最后两步之一存在阻断。已知的亚铁螯合酶突变体对C54的互补作用表明,缺陷最可能存在于编码原卟啉原氧化酶的HEM14中。通过用酵母基因组质粒文库转化获得了一个能够互补C54的质粒。插入片段的部分序列将该基因鉴定为酵母染色体V的阅读框YER014(GenBank登录号U18778)。这个阅读框编码一种与人类原卟啉原氧化酶同源的蛋白质。该基因的破坏引发呼吸缺陷和原卟啉积累。无效突变体的表型以及YER014p与人类原卟啉原氧化酶的同源性提供了令人信服的证据,证明YER014就是HEM14。