Souza A E, Shu H H, Read L K, Myler P J, Stuart K D
Seattle Biomedical Research Institute, Washington 98109-1651.
Mol Cell Biol. 1993 Nov;13(11):6832-40. doi: 10.1128/mcb.13.11.6832-6840.1993.
Several genes of the Trypanosoma brucei mitochondrial genome (the maxicircle) encode mRNAs that are so extensively altered by RNA editing that the gene cannot be identified by analysis of the DNA sequence. The 322-nucleotide preedited RNA of one of these genes, CR2, is converted into a 647-nucleotide transcript by the addition of 345 uridines and the deletion of 20 genomically encoded uridines. The fully edited transcript has an open reading frame that predicts a 194-amino-acid protein. This protein, which we name ND9 (NADH dehydrogenase subunit 9), has homology to a subunit of NADH dehydrogenase (respiratory complex I). Seven guide RNAs that can specify edited CR2 sequence have been identified. Steady-state levels of unedited ND9 transcripts are greater in bloodstream than in procyclic forms, but edited ND9 mRNA is present in similar abundance in both life cycle stages.
布氏锥虫线粒体基因组(大环状DNA)中的几个基因所编码的mRNA会因RNA编辑而发生广泛改变,以至于无法通过DNA序列分析来识别该基因。其中一个基因CR2的322个核苷酸的未编辑RNA,通过添加345个尿苷和删除20个基因组编码的尿苷,被转化为一个647个核苷酸的转录本。完全编辑后的转录本有一个开放阅读框,预测会产生一种194个氨基酸的蛋白质。我们将这种蛋白质命名为ND9(NADH脱氢酶亚基9),它与NADH脱氢酶(呼吸复合体I)的一个亚基具有同源性。已经鉴定出7种能够指定编辑后CR2序列的引导RNA。未编辑的ND9转录本在血流形式中的稳态水平高于前循环形式,但编辑后的ND9 mRNA在两个生命周期阶段中的丰度相似。