Lelandais C, Albert B, Gutierres S, De Paepe R, Godelle B, Vedel F, Chétrit P
Institut de Biotechnologie des Plantes, Université Paris-Sud, 91405 Orsay Cedex, France.
Genetics. 1998 Oct;150(2):873-82. doi: 10.1093/genetics/150.2.873.
Previous analyses suggested that the Nicotiana sylvestris CMSII mutant carried a large deletion in its mitochondrial genome. Here, we show by cosmid mapping that the deletion is 60 kb in length and contains several mitochondrial genes or ORFs, including the complex I nad7 gene. However, due to the presence of large duplications in the progenitor mitochondrial genome, the only unique gene that appears to be deleted is nad7. RNA gel blot data confirm the absence of nad7 expression, strongly suggesting that the molecular basis for the CMSII abnormal phenotype, poor growth and male sterility, is the altered complex I structure. The CMSII mitochondrial genome appears to consist essentially of one of two subgenomes resulting from recombination between direct short repeats. In the progenitor mitochondrial genome both recombination products are detected by PCR and, reciprocally, the parental fragments are detected at the substoichiometric level in the mutant. The CMSII mtDNA organization has been maintained through six sexual generations.
先前的分析表明,野生烟草CMSII突变体的线粒体基因组存在大片段缺失。在此,我们通过粘粒作图显示,该缺失长度为60 kb,包含几个线粒体基因或开放阅读框(ORF),包括复合体I的nad7基因。然而,由于祖先线粒体基因组中存在大量重复序列,唯一似乎被删除的独特基因是nad7。RNA凝胶印迹数据证实不存在nad7表达,强烈表明CMSII异常表型、生长不良和雄性不育的分子基础是复合体I结构改变。CMSII线粒体基因组似乎基本上由直接短重复序列之间重组产生的两个亚基因组之一组成。在祖先线粒体基因组中,通过PCR可检测到两种重组产物,相反,在突变体中以亚化学计量水平检测到亲本片段。CMSII线粒体DNA的组织形式已通过六个有性世代得以维持。