Waśkiewicz-Staniorowska B, Skała J, Jasiński M, Grenson M, Goffeau A, Ułaszewski S
Institute of Microbiology, Wroclaw University, Poland.
Yeast. 1998 Aug;14(11):1027-39. doi: 10.1002/(SICI)1097-0061(199808)14:11<1027::AID-YEA295>3.0.CO;2-S.
A 7.24 kb genomic DNA fragment from the yeast Saccharomyces cerevisiae chromosome XVI was isolated by complementation of a new temperature-sensitive mutation tsa1. We determined the nucleotide sequence of this fragment located on the right arm of chromosome XVI. Among the three, complete open reading frames: YPR041w, YPR042c and YPR043w contained within this fragment, the gene YPR041w was shown to complement the tsa1 mutation and to correspond to the TIF5 gene encoding an essential protein synthesis initiation translation factor. The YPR042c gene encodes a hypothetical protein of 1075 amino acids containing four putative transmembrane segments and is non-essential for growth. The gene YPR043c encoding the 10 kDa product, highly similar to the human protein L37a from the 60S ribosomal subunit, was found to be essential and a dominant lethal. We conclude that three tightly linked yeast genes are involved in the translation process.
通过对一种新的温度敏感突变体tsa1进行互补,从酿酒酵母第十六条染色体中分离出一个7.24 kb的基因组DNA片段。我们确定了位于第十六条染色体右臂上的该片段的核苷酸序列。在该片段包含的三个完整开放阅读框YPR041w、YPR042c和YPR043w中,基因YPR041w被证明可互补tsa1突变,并对应于编码一种必需的蛋白质合成起始翻译因子的TIF5基因。YPR042c基因编码一种含有四个假定跨膜区段的1075个氨基酸的假定蛋白质,对生长非必需。编码10 kDa产物且与来自60S核糖体亚基的人类蛋白质L37a高度相似的YPR043c基因被发现是必需的且具有显性致死性。我们得出结论,三个紧密连锁的酵母基因参与了翻译过程。