Köck J, Evers R, Cornelissen A W
Max-Planck-Institut für Biologie, Molecular Parasitology Unit, Tübingen, FRG.
Nucleic Acids Res. 1988 Sep 26;16(18):8753-72. doi: 10.1093/nar/16.18.8753.
As the first step in the analysis of the transcription process in the African trypanosome, Trypanosoma brucei, we have started to characterise the trypanosomal RNA polymerases. We have previously described the gene encoding the largest subunit of RNA polymerase II and found that two almost identical RNA polymerase II genes are encoded within the genome of T. brucei. Here we present the identification, cloning and sequence analysis of the gene encoding the largest subunit of RNA polymerase III. This gene contains a single open reading frame encoding a polypeptide with a Mr of 170 kD. In total, eight encoding a polypeptide with a Mr of 170 kD. In total, eight highly conserved regions with significant homology to those previously reported in other eukaryotic RNA polymerase largest subunits were identified. Some of these domains contain functional sites, which are conserved among all eukaryotic largest subunit genes analysed thus far. Since these domains make up a large part of each polypeptide, independent of the RNA polymerase class, these data strongly support the hypothesis that these domains provide a major part of the transcription machinery of the RNA polymerase complex. The additional domains which are uniquely present in the largest subunit of RNA polymerase I and II, respectively, two large hydrophylic insertions and a C-terminal extension, might be a determining factor in specific transcription of the gene classes.
作为分析非洲锥虫(布氏锥虫)转录过程的第一步,我们已开始对锥虫RNA聚合酶进行特性描述。我们之前描述过编码RNA聚合酶II最大亚基的基因,并发现布氏锥虫基因组中编码了两个几乎相同的RNA聚合酶II基因。在此,我们展示了对编码RNA聚合酶III最大亚基基因的鉴定、克隆及序列分析。该基因包含一个单一的开放阅读框,编码一个分子量为170 kD的多肽。总共鉴定出八个与其他真核生物RNA聚合酶最大亚基中先前报道的区域具有显著同源性的高度保守区域。其中一些结构域包含功能位点,这些位点在迄今为止分析的所有真核生物最大亚基基因中都是保守的。由于这些结构域构成了每个多肽的很大一部分,与RNA聚合酶类别无关,这些数据有力地支持了这样一种假说,即这些结构域构成了RNA聚合酶复合物转录机制的主要部分。分别在RNA聚合酶I和II最大亚基中独特存在的额外结构域,即两个大的亲水性插入序列和一个C末端延伸,可能是基因类别特异性转录的决定因素。