Gao G, Kapushoc S T, Simpson A M, Thiemann O H, Simpson L
Howard Hughes Medical Institute, University of California, Los Angeles, 90095, USA.
RNA. 2001 Sep;7(9):1335-47. doi: 10.1017/s1355838201018076.
Guide RNAs (gRNAs) are encoded both in the maxicircle and minicircle components of the mitochondrial DNA of trypanosomatid protozoa. These RNAs mediate the precise insertion and deletion of U residues in transcripts of the maxicircle DNA. We showed previously that the old UC laboratory strain of Leishmania tarentolae apparently lost more than 40 minicircle-encoded gRNAs that are present in the recently isolated LEM125 strain (Thiemann et al., EMBO J, 1994, 13:5689-5700]. We have further analyzed the population of minicircle-encoded gRNAs in the LEM125 strain. Sau3AI and MspI minicircle libraries were constructed and screened for novel gRNAs by negative colony hybridization. This search yielded 20 minicircles encoding new gRNAs that covered most of the remaining gaps in the editing cascades of the ND8, ND9, G4, and G5 genes, and in addition, more than 30 minicircles containing either unassigned or undetectable gRNA genes. We also completely sequenced 34 of the 45 minicircle sequence classes encoding previously identified gRNAs. A total of 19 pairs of redundant gRNAs, which are gRNAs of different sequences covering the same editing blocks, were identified. The gRNAs in each redundant pair generally had different relative abundances and different extents of mismatches with edited sequences. Alignments of the minicircles encoding redundant gRNAs yielded 59 to 93% matching nucleotides, suggesting an origin from duplication of ancestral minicircles and subsequent genetic drift. We propose a functional explanation for the existence of redundant gRNAs in this strain.
引导RNA(gRNA)由锥虫原生动物线粒体DNA的大环和小环成分编码。这些RNA介导大环DNA转录本中U残基的精确插入和缺失。我们之前表明,利什曼原虫的旧UC实验室菌株显然丢失了最近分离的LEM125菌株中存在的40多种小环编码的gRNA(Thiemann等人,《欧洲分子生物学组织杂志》,1994年,13:5689 - 5700)。我们进一步分析了LEM125菌株中小环编码的gRNA群体。构建了Sau3AI和MspI小环文库,并通过阴性菌落杂交筛选新的gRNA。该搜索产生了20个编码新gRNA的小环,它们覆盖了ND8、ND9、G4和G5基因编辑级联中大部分剩余的缺口,此外,还有30多个包含未分配或不可检测gRNA基因的小环。我们还对45个编码先前鉴定的gRNA的小环序列类别中的34个进行了全序列测定。总共鉴定出19对冗余gRNA,即覆盖相同编辑块的不同序列的gRNA。每个冗余对中的gRNA通常具有不同的相对丰度和与编辑序列不同程度的错配。编码冗余gRNA的小环比对产生59%至93%的匹配核苷酸,表明其起源于祖先小环的复制和随后的遗传漂变。我们对该菌株中冗余gRNA的存在提出了一种功能解释。