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影响酿酒酵母主要甘氨酸转运RNA的移码抑制突变。

Frameshift suppressor mutations affecting the major glycine transfer RNAs of Saccharomyces cerevisiae.

作者信息

Mendenhall M D, Leeds P, Fen H, Mathison L, Zwick M, Sleiziz C, Culbertson M R

出版信息

J Mol Biol. 1987 Mar 5;194(1):41-58. doi: 10.1016/0022-2836(87)90714-5.

Abstract

Mutations have been identified in Saccharomyces cerevisiae glycine tRNA genes that result in suppression of +1 frameshift mutations in glycine codons. Wild-type and suppressor alleles of genes encoding the two major glycine tRNAs, tRNA(GCC) and tRNA(UCC), were examined in this study. The genes were identified by genetic complementation and by hybridization to a yeast genomic library using purified tRNA probes. tRNA(UCC) is encoded by three genes, whereas approximately 15 genes encode tRNA(GCC). The frameshift suppressor genes suf1+, suf4+ and suf6+ were shown to encode the wild-type tRNA(UCC) tRNA. The suf1+ and suf4+ genes were identical in DNA sequence, whereas the suf6+ gene, whose DNA sequence was not determined, was shown by a hybridization experiment to encode tRNA(UCC). The ultraviolet light-induced SU F1-1 and spontaneous SU F4-1 suppressor mutations were each shown to differ from wild-type at two positions in the anticodon, including a +1 base-pair insertion and a base-pair substitution. These changes resulted in a CCCC four-base anticodon rather than the CCU three-base anticodon found in wild-type. The RNA sequence of tRNA(UCC) was shown to contain a modified uridine in the wobble position. Mutant tRNA(CCCC) isolated from a SU F1-1 strain lacked this modification. Three unlinked genes that encode wild-type tRNA(GCC), suf20+, trn2, and suf17+, were identical in DNA sequence to the previously described suf16+ frameshift suppressor gene. Spontaneous suppressor mutations at the SU F20 and SU F17 loci were analyzed. The SU F20-2 suppressor allele contained a CCCC anticodon. This allele was derived in two serial selections through two independent mutational events, a +1 base insertion and a base substitution in the anticodon. Presumably, the original suppressor allele, SU F20-1, contained the single base insertion. The SU F17-1 suppressor allele also contained a CCCC anticodon resulting from two mutations, a +1 insertion and a base substitution. However, this allele contained an additional base substitution at position 33 adjacent to the 5' side of the four-base anticodon. The possible origin and significance of multiple mutations leading to frameshift suppression is discussed.

摘要

在酿酒酵母甘氨酸tRNA基因中已鉴定出导致甘氨酸密码子中+1移码突变抑制的突变。本研究检测了编码两种主要甘氨酸tRNA(tRNA(GCC)和tRNA(UCC))的基因的野生型和抑制等位基因。通过遗传互补以及使用纯化的tRNA探针与酵母基因组文库杂交来鉴定这些基因。tRNA(UCC)由三个基因编码,而大约15个基因编码tRNA(GCC)。移码抑制基因suf1+、suf4+和suf6+被证明编码野生型tRNA(UCC)。suf1+和suf4+基因的DNA序列相同,而suf6+基因(其DNA序列未确定)通过杂交实验被证明编码tRNA(UCC)。紫外线诱导的SU F1-1和自发的SU F4-1抑制突变在反密码子的两个位置上均与野生型不同,包括一个+1碱基对插入和一个碱基对替换。这些变化导致了一个CCCC四碱基反密码子,而不是野生型中的CCU三碱基反密码子。tRNA(UCC)的RNA序列显示在摆动位置含有一个修饰的尿苷。从SU F1-1菌株中分离出的突变tRNA(CCCC)缺乏这种修饰。三个编码野生型tRNA(GCC)的不连锁基因suf20+、trn2和suf17+,其DNA序列与先前描述的suf16+移码抑制基因相同。分析了SU F20和SU F17位点的自发抑制突变。SU F20-2抑制等位基因含有一个CCCC反密码子。该等位基因通过两个独立的突变事件在两次连续选择中产生,一个是反密码子中的+1碱基插入和一个碱基替换。推测原始抑制等位基因SU F20-1含有单个碱基插入。SU F17-1抑制等位基因也含有一个由两个突变产生的CCCC反密码子,一个是+1插入和一个碱基替换。然而,该等位基因在四碱基反密码子5'侧相邻的33位还含有一个额外的碱基替换。讨论了导致移码抑制的多个突变的可能起源和意义。

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