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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Suppression of a Nuclear aep2 Mutation in Saccharomyces cerevisiae by a Base Substitution in the 5′-Untranslated Region of the Mitochondrial oli1 Gene Encoding Subunit 9 of ATP Synthase
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Suppression of a Nuclear aep2 Mutation in Saccharomyces cerevisiae by a Base Substitution in the 5′-Untranslated Region of the Mitochondrial oli1 Gene Encoding Subunit 9 of ATP Synthase

机译:通过编码ATP合酶亚基9的线粒体oli1基因的5'-非翻译区的碱基取代来抑制酿酒酵母中的核aep2突变。

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Mutations in the nuclear AEP2 gene of Saccharomyces generate greatly reduced levels of the mature form of mitochondrial oli1 mRNA, encoding subunit 9 of mitochondrial ATP synthase. A series of mutants was isolated in which the temperature-sensitive phenotype resulting from the aep2-ts1 mutation was suppressed. Three strains were classified as containing a mitochondrial suppressor: these lost the ability to suppress aep2-ts1 when their mitochondrial genome was replaced with wild-type mitochondrial DNA (mtDNA). Many other isolates were classified as containing dominant nuclear suppressors. The three mitochondrion-encoded suppressors were localized to the oli1 region of mtDNA using rho – genetic mapping techniques coupled with PCR analysis; DNA sequencing revealed, in each case, a T-to-C nucleotide transition in mtDNA 16 nucleotides upstream of the oli1 reading frame. It is inferred that the suppressing mutation in the 5′ untranslated region of oli1 mRNA restores subunit 9 biosynthesis by accommodating the modified structure of Aep2p generated by the aep2-ts1 mutation (shown here to cause the substitution of proline for leucine at residue 413 of Aep2p). This mode of mitochondrial suppression is contrasted with that mediated by heteroplasmic rearranged rho – mtDNA genomes bypassing the participation of a nuclear gene product in expression of a particular mitochondrial gene. In the present study, direct RNA-protein interactions are likely to form the basis of suppression.
机译:酿酒酵母的核AEP2基因突变产生的线粒体oli1 mRNA成熟形式的水平大大降低,编码线粒体ATP合酶的9亚基。分离出一系列突变体,其中aep2-ts1突变引起的温度敏感性表型被抑制。三种菌株被分类为含有线粒体抑制剂:当它们的线粒体基因组被野生型线粒体DNA(mtDNA)取代时,它们丧失了抑制aep2-ts1的能力。许多其他分离株被分类为含有主要的核抑制剂。使用rho-遗传作图技术结合PCR分析,将三个线粒体编码的抑制子定位到mtDNA的oli1区。 DNA测序揭示了在每种情况下oli1阅读框上游mtDNA 16个核苷酸中的T到C核苷酸过渡。推测oli1 mRNA 5'非翻译区的抑制性突变通过容纳由aep2-ts1突变产生的Aep2p的修饰结构来恢复亚基9的生物合成(此处显示在Aep2p的第413位残基上脯氨酸被亮氨酸取代) )。线粒体抑制的这种模式与异质重排的rh-mtDNA基因组介导的模式相反,该基因组绕过了核基因产物参与特定线粒体基因的表达。在本研究中,直接的RNA-蛋白质相互作用很可能构成抑制的基础。

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