Dunstan H M, Green-Willms N S, Fox T D
Section of Genetics and Development, Cornell University, Ithaca, New York 14853-2703, USA.
Genetics. 1997 Sep;147(1):87-100. doi: 10.1093/genetics/147.1.87.
We have used mutational and revertant analysis to study the elements of the 54-nucleotide COX2 5'-untranslated leader involved in translation initiation in yeast mitochondria and in activation by the COX2 translational activator. Pet111p. We generated a collection of mutants with substitutions spanning the entire COX2 5'-UTL by in vitro mutagenesis followed by mitochondrial transformation and gene replacement. The phenotypes of these mutants delimit a 31-nucleotide segment, from -16 to -46, that contains several short sequence elements necessary for COX2 5'-UTL function in translation. The sequences from -16 to -47 were shown to be partially sufficient to promote translation in a foreign context. Analysis of revertants of both the series of linker-scanning alleles and two short deletion/ insertion alleles has refined the positions of several possible functional elements of the COX2 5'-untranslated leader, including a putative RNA stem-loop structure that functionally interacts with Pet111p and an octanucleotide sequence present in all S. cerevisiae mitochondrial mRNA 5'-UTLs that is a potential rRNA binding site.
我们利用突变和回复突变分析来研究酵母线粒体中参与翻译起始以及被COX2翻译激活因子Pet111p激活的54个核苷酸的COX2 5'-非翻译前导序列的元件。我们通过体外诱变,随后进行线粒体转化和基因替换,生成了一系列跨越整个COX2 5'-UTL的取代突变体。这些突变体的表型界定了一个从-16到-46的31个核苷酸的片段,该片段包含COX2 5'-UTL在翻译中发挥功能所需的几个短序列元件。从-16到-47的序列被证明在一定程度上足以在异源环境中促进翻译。对一系列接头扫描等位基因以及两个短缺失/插入等位基因的回复突变体的分析,进一步明确了COX2 5'-非翻译前导序列几个可能的功能元件的位置,包括一个与Pet111p发生功能相互作用的假定RNA茎环结构,以及所有酿酒酵母线粒体mRNA 5'-UTL中都存在的一个八核苷酸序列,该序列是一个潜在的rRNA结合位点。