Genetisches Institut der Universität München, Maria-Ward-Strasse 1a, D-8000, München 19, Germany.
Curr Genet. 1980 Feb;1(2):155-61. doi: 10.1007/BF00446961.
Electrophoretic separation of mitochondrial RNA followed by hybridization with restriction fragments of mtDNA has been used to identify transcripts of the split gen COB which codes for apocytochrome b.In wild type a major transcript of 18S is detected besides a 10S RNA and a series of transcripts with electrophoretic mobilities higher than 18S. Mutations in coding sequences do not significantly alter this transcript pattern. In contrast, mutations in intervening sequences give rise to different patterns: The 18S RNA, the putative messenger for apocytochrome b, is lacking; depending on the intervening sequence affected by mutation, one or the other of the larger transcripts (23S, 24S, 32S, 34S) is accumulated instead. In most mutants a 10S RNA species is present; it has not been detected, however, in case of a small cluster of mutations which lead to the accumulation of the largest transcript (34S) observed, which most likely contains all coding and intervening sequences of the split gene COB.These results suggest a pathway of splicing.
采用电泳分离线粒体 RNA 并用 mtDNA 的限制酶片段进行杂交的方法,鉴定了编码细胞色素 b 脱辅基蛋白的分裂基因 COB 的转录物。在野生型中,除了 10S RNA 和一系列电泳迁移率高于 18S 的转录物外,还检测到 18S 的主要转录物。编码序列中的突变不会显著改变这种转录物模式。相比之下,内含子中的突变会产生不同的模式:缺乏 18S RNA,即细胞色素 b 的假定信使 RNA;根据受突变影响的内含子,较大的转录物(23S、24S、32S、34S)之一或另一个会累积。在大多数突变体中存在 10S RNA 种类;然而,在导致观察到最大转录物(34S)积累的一小簇突变中,未检测到该 RNA,这最有可能包含分裂基因 COB 的所有编码和内含子序列。这些结果表明存在剪接途径。