Yasuhira S, Simpson L
Howard Hughes Medical Institute, University of California, Los Angeles 90095-1662, USA.
RNA. 1996 Nov;2(11):1153-60.
Trypanoplasma borreli belongs to the bodonid/cryptobiid group of kinetoplastid protozoa, which represents a sister group to the trypanosomatids. RNA transcripts from several mitochondrial genes in this organism undergo the trypanosomatid type of uridine addition/deletion RNA editing. A guide RNA (gRNA) cDNA library was constructed and five gRNAs were identified, one for editing the ribosomal protein S12 mRNA, three for editing the cytochrome oxidase subunit I mRNA, and one for editing the cytochrome b mRNA. All of the gRNAs contained nonencoded oligo[U] sequences at the 3' end, as is common with gRNAs in trypanosomatids, but also contained nonencoded oligo[U] sequences at the 5' end. The mechanism for addition of the 5' nonencoded oligo[U] sequence and the function of this sequence are unknown. The T. borreli gRNAs were shorter (25-35 nt, excluding the 5' oligo[U]) than gRNAs in trypanosomatids (45-50 nt), indicating a smaller size of editing blocks in this organism. Genomic sequences for two gRNAs were cloned and sequenced. These two gRNA-encoding sequences were shown to originate from the 180-kb Component I molecules, which represent a possible homologue of minicircle DNA in trypanosomatids, and not from the 80-kb Component II molecules, which contain the structural genes and cryptogenes.
博氏锥虫属于动质体原生动物的波豆虫/隐滴虫类群,该类群是锥虫类的姐妹群。该生物体中几个线粒体基因的RNA转录本经历锥虫类的尿苷添加/缺失RNA编辑。构建了一个向导RNA(gRNA)cDNA文库,并鉴定出5种gRNA,一种用于编辑核糖体蛋白S12 mRNA,三种用于编辑细胞色素氧化酶亚基I mRNA,一种用于编辑细胞色素b mRNA。所有gRNA在3'端都含有非编码的寡聚[U]序列,这与锥虫类中的gRNA相同,但在5'端也含有非编码的寡聚[U]序列。5'非编码寡聚[U]序列的添加机制及其功能尚不清楚。博氏锥虫的gRNA比锥虫类中的gRNA短(25 - 35个核苷酸,不包括5'寡聚[U]),表明该生物体中编辑块的大小较小。克隆并测序了两种gRNA的基因组序列。这两个编码gRNA的序列显示源自180 kb的组分I分子,其代表锥虫类中微小环DNA的可能同源物,而非源自含有结构基因和隐蔽基因的80 kb组分II分子。