Kang Y W, Miller D L
Biology Programs, University of Texas at Dallas, Richardson 75083-0688.
Mol Gen Genet. 1988 Aug;213(2-3):425-34. doi: 10.1007/BF00339612.
We isolated revertants capable of respiration from the respiratory deficient yeast mutant, FF1210-6C/170, which displays greatly decreased mitochondrial protein synthesis due to a single base substitution at the penultimate base of the tRNAAsp gene on mitochondrial (mt) DNA. Three classical types of revertant were identified: (1) same-site revertants; (2) intragenic revertants which restore the base pairing in the acceptor stem of the mitochondrial tRNAAsp; and (3) extragenic suppressors located in nuclear DNA. In addition a fourth type of revertant was identified in which the mutant tRNAAsp is amplified due to the maintenance of both the original mutant mtDNA and a modified form of the mutant mtDNA in which only a small region around the tRNAAsp gene is retained and amplified. The latter form resembles the mtDNA in vegetative petite (rho-) strains which normally segregates rapidly from the wild-type mtDNA. Each revertant type was characterized genetically and by both DNA sequence analysis of the mitochondrial tRNAAsp gene and analysis of the quantity and size of RNA containing the tRNAAsp sequence. These results indicate that the mitochondrial tRNAAsp of the mutant retains a low level of activity and that the presence of the terminal base pair in tRNAAsp is a determinant of both tRNAAsp function and the maintenance of wild-type levels of tRNAAsp.
我们从呼吸缺陷型酵母突变体FF1210 - 6C/170中分离出了能够进行呼吸作用的回复突变体。该突变体由于线粒体(mt)DNA上天冬氨酸tRNA(tRNAAsp)基因倒数第二个碱基处的单个碱基替换,导致线粒体蛋白质合成大幅减少。我们鉴定出了三种经典类型的回复突变体:(1)同一位点回复突变体;(2)恢复线粒体tRNAAsp接受臂碱基配对的基因内回复突变体;(3)位于核DNA中的基因外抑制子。此外,还鉴定出了第四种类型的回复突变体,其中突变的tRNAAsp由于原始突变型mtDNA和突变型mtDNA的一种修饰形式的同时存在而被扩增,在这种修饰形式中,仅tRNAAsp基因周围的一小区域被保留并扩增。后一种形式类似于营养型小菌落(rho-)菌株中的mtDNA,其通常会迅速从野生型mtDNA中分离出来。每种回复突变体类型都通过遗传学方法进行了表征,并对线粒体tRNAAsp基因进行了DNA序列分析,同时分析了含有tRNAAsp序列的RNA的数量和大小。这些结果表明,突变体的线粒体tRNAAsp保留了低水平的活性,并且tRNAAsp中末端碱基对的存在是tRNAAsp功能以及野生型tRNAAsp水平维持的一个决定因素。