Dobres M, Gerbl-Rieger S, Schmelzer C, Mueller M W, Schweyen R J
Institute für Genetik und Mikrobiologie, Universität München, Federal Republic of Germany.
Curr Genet. 1985;10(4):283-90. doi: 10.1007/BF00365624.
Two cob- deletion mutants are characterized. One of them, M9410, is deleted for 911 bp of the noncoding sequences only which separate tRNAGlu and cob exon 1; it thus lacks most of the sequence encoding the 957 bp long cob leader (Bonitz et al. 1982) and some 20 bp 5' to it. The end points of this deletion coincide with 31 bp long direct repeats in wild type mtDNA. The other mutant, M9391, is deleted for all cob coding sequences and most of the cob leader sequence but it retains the 5' terminal 261 bp of this leader. Northern analysis revealed that M9410 totally lacks cob mRNA or pre-mRNA. The large deletion M9391 in contrast accumulates a 13S RNA which probably results from transcription through the junction, which ligates sequences of the cob leader to sequences of the cob-oli1 intergenic spacer.
对两个cob基因缺失突变体进行了表征。其中一个突变体M9410,仅缺失了位于tRNAGlu和cob外显子1之间的911 bp非编码序列;因此它缺少了编码957 bp长的cob前导序列的大部分序列(博尼茨等人,1982年)以及其5'端约20 bp的序列。该缺失的端点与野生型线粒体DNA中31 bp长的正向重复序列一致。另一个突变体M9391,缺失了所有cob编码序列和大部分cob前导序列,但保留了该前导序列5'端的261 bp。Northern分析表明,M9410完全缺乏cob mRNA或前体mRNA。相比之下,大缺失突变体M9391积累了一种13S RNA,这可能是由于转录通过了连接点,该连接点将cob前导序列与cob-oli1基因间隔区的序列连接起来。