Carignani G, Dujardin G, Slonimski P P
Mol Gen Genet. 1979 Jan 2;167(3):301-8. doi: 10.1007/BF00267423.
Fifty eight mitochondrial mutants (p + mit- mutants), all deficient in cytochrome oxidase activity and previously assigned to the genetic region oxi3 on the mitochondrial DNA, were mapped by the method of "petite deletion mapping". This procedure resulted in the identification of at least twenty one different classes of oxi3 mutants, which could be arranged in a linear order. Moreover, it provided a set of twenty three p- petite mutants, each containing a differentially deleted mit DNA segment included in the oxi3 region. The two sets of mutants, p+ oxi3- and p- oxi3+, will be of interest for a further genetic and physical analysis of this mitochondrial DNA segment which spans over about ten thousand base pairs and controls the subunit I of cytochrome oxidase.
58个线粒体突变体(p⁺ mit⁻ 突变体),均缺乏细胞色素氧化酶活性,且先前已被定位到线粒体DNA上的oxi3遗传区域,通过“小缺失图谱绘制”方法进行了定位。该程序确定了至少21种不同类别的oxi3突变体,它们可以按线性顺序排列。此外,它还提供了一组23个p⁻ 小菌落突变体,每个突变体都包含oxi3区域内差异缺失的线粒体DNA片段。这两组突变体,p⁺ oxi3⁻ 和p⁻ oxi3⁺,对于进一步对跨越约一万个碱基对并控制细胞色素氧化酶亚基I的该线粒体DNA片段进行遗传和物理分析将具有重要意义。