Zhuravleva G A, Moskalenko S E, Murina O A, Inge-Vechtomov S G
Genetika. 2007 Oct;43(10):1363-71.
Nonlethal nonsense mutations obtained earlier in the essential gene SUP45 encoding the translation termination eRFI factor in the yeast Saccharomyces cerevisiae were further characterized. Strains carrying these mutations retain the viability, since the full-length eRF1 protein is present in these strains, although in decreased amounts as compared to wild-type cells, together with a truncated eRF1. All nonsense mutations are likely to be located in a weak termination context, because a change in the stop codon UGAA (in the case of mutation sup45-107) to UAGA (sup45-107.2) led to the alteration of the local context from a weak to strong and to the lethality of the strain carrying sup45-107.2. All nonsense mutations studied are characterized by thermosensitivity expressed as cell mortality after cultivation at 37 degrees C. When grown under nonpermissive conditions (37 degrees C), cells of nonsense mutants sup45-104, sup45-105. and sup45-107 display a decrease in the amount of the truncated eRF1 protein without reduction in the amount of the full-length eRF1 protein. The results of this study suggest that the N-terminal eRF1 fragment is indispensable for cell viability of nonsense mutants due to the involvement in termination of translation.
对酿酒酵母中编码翻译终止因子eRF1的必需基因SUP45早期获得的非致死性无义突变进行了进一步表征。携带这些突变的菌株仍具有活力,因为这些菌株中存在全长eRF1蛋白,尽管与野生型细胞相比数量减少,同时还有截短的eRF1。所有无义突变可能都位于弱终止背景中,因为终止密码子UGAA(在突变sup45 - 107的情况下)变为UAGA(sup45 - 107.2)导致局部背景从弱变为强,并导致携带sup45 - 107.2的菌株致死。所研究的所有无义突变的特征都是热敏感性,表现为在37℃培养后的细胞死亡率。在非允许条件(37℃)下生长时,无义突变体sup45 - 104、sup45 - 105和sup45 - 107的细胞中截短的eRF1蛋白量减少,而全长eRF1蛋白量没有减少。这项研究的结果表明,由于参与翻译终止,N端eRF1片段对于无义突变体的细胞活力是不可或缺的。