Laboratory of Physiological Chemistry, State University, Bloemsingel 10, 9712 KZ, Groningen, The Netherlands.
Curr Genet. 1981 Jul;3(3):205-11. doi: 10.1007/BF00429822.
[E35], an extranuclear mutant of Neurospora crassa has all the phenotypic characteristics of the "stopper" mutants (De Vries et al. 1980). In the present work, the mitochondrial DNA as well as the mitochondrial translation products are characterized further. The primary mutational event appears to have been the deletion of about 4 kbp from the wild-type genome. Moreover, after prolonged vegetative growth the mutant accumulates an 8-μm circular mtDNA, which was demonstrated both by electronmicroscopy and by restriction enzyme analysis. Hence, the mutant contains two populations of aberrant mitochondrial DNA, the smaller of which is an amplification of the rRNA-tRNA part of the larger. We propose that the primary deletion has generated a signal in the larger DNA which can cause premature termination of replication at the deletion site, and subsequent circularization of the unfinished daughter molecule. Finally, the deleted part may contain a determinant for synthesis of a protein of 11 kDal. The function of this protein, which is not a subunit of the F0 ATPase, is not yet known.
[E35],粗糙脉孢菌的一种核外突变体,具有“阻遏突变体”(De Vries 等人,1980)的所有表型特征。在本工作中,进一步对线粒体 DNA 及其线粒体翻译产物进行了表征。初步突变事件似乎是从野生型基因组中缺失了约 4 kbp。此外,在长时间的营养生长后,突变体积累了一个 8 μm 的圆形 mtDNA,这一点通过电子显微镜和限制性内切酶分析得到了证明。因此,突变体含有两种异常的线粒体 DNA 群体,较小的群体是较大群体的 rRNA-tRNA 部分的扩增。我们提出,最初的缺失在较大的 DNA 中产生了一个信号,该信号可以导致在缺失部位复制的过早终止,并随后使未完成的子链环化。最后,缺失部分可能包含一个决定合成 11 kDal 蛋白的决定因素。该蛋白不是 F0 ATP 酶的亚基,其功能尚不清楚。