Kang Y W, Miller D L
Biology Program, University of Texas, Richardson 75083-0688.
Nucleic Acids Res. 1989 Nov 11;17(21):8595-609. doi: 10.1093/nar/17.21.8595.
Saccharomyces cerevisiae strain FF1210-6C/170 is respiratory deficient due to a mutation of the penultimate base of the mitochondrial tRNA(Asp) gene. We have identified a number of progeny from this strain which have reverted to respiratory sufficiency by the excision and tandem amplification of a small region of the mitochondrial (mt) DNA carrying the tRNA(Asp) gene, while also maintaining the full-length mtDNA. We have studied the structure of the mtDNA and mitochondrial transcription in a number of these heteroplasmic strains. The exact site of the recombination involved in the excision of the repeating unit of the amplified mtDNA has been determined for five of the revertants. Recombination occurs between identical sequences 4-13 base pairs in length. Each of the different repeating units of the amplified DNA retains an active promoter which has been moved to a site just upstream of the tRNA(Asp) gene by the excision/amplification. Transcripts from the heteroplasmic strains have been characterized to determine the sites of mitochondrial RNA termini. We find that in addition to the 5' and 3' processing of the tRNAs, many of the transcripts terminate at a position about 300 base pairs downstream of the gene for tRNA(Asp). We also find that 3' processing of tRNA(Asp) precursors is absent in petite strains which lack 5' processing indicating that 5' processing of tRNA(Asp) may be a prerequisite for 3' processing in this mutant.
酿酒酵母菌株FF1210 - 6C/170因线粒体天冬氨酸转运RNA(tRNAAsp)基因倒数第二个碱基发生突变而呼吸缺陷。我们已鉴定出该菌株的一些子代,它们通过切除并串联扩增携带tRNAAsp基因的线粒体(mt)DNA小区域而恢复为呼吸充足,同时还保留了全长mtDNA。我们研究了许多这些异质菌株中的mtDNA结构和线粒体转录。已确定五个回复突变体中涉及扩增mtDNA重复单元切除的重组确切位点。重组发生在长度为4 - 13个碱基对的相同序列之间。扩增DNA的每个不同重复单元都保留一个活性启动子,该启动子通过切除/扩增已移动到tRNAAsp基因上游的一个位点。已对异质菌株的转录本进行了表征,以确定线粒体RNA末端的位点。我们发现,除了tRNA的5'和3'加工外,许多转录本在tRNAAsp基因下游约300个碱基对的位置终止。我们还发现,在缺乏5'加工的小菌落菌株中不存在tRNAAsp前体的3'加工,这表明tRNAAsp的5'加工可能是该突变体中3'加工的先决条件。