Allmansberger R, Bokranz M, Kröckel L, Schallenberg J, Klein A
Department of Biology, Philipps University, Marburg, Federal Republic of Germany.
Can J Microbiol. 1989 Jan;35(1):52-7. doi: 10.1139/m89-008.
A comparative analysis of cotranscribed gene clusters comprising the structural genes mcrA, mcrB, mcrC, mcrD, and mcrG was carried out in three species of methanogens. mcrA, mcrB, and mcrG are the structural genes for the three subunits of methyl coenzyme M reductase, while the two other genes encode polypeptides of unknown functions. The degree of conservation of the mcr gene products among different species of methanogens varies. No correlation was found between the conservation of the G+C contents of the homologous genes and of the amino acid sequences of their products among the different bacteria. The comparison of RNA polymerase core subunit genes of Methanobacterium thermoautotrophicum as evolutionary markers with their equivalents in Escherichia coli, Saccharomyces cerevisiae, and Drosophila melanogaster showed that homologous polypeptide domains are encoded by different numbers of genes suggesting gene fusion of adjacent genes in the course of evolution. The archaebacterial subunits exhibit much stronger homology with their eukaryotic than with their eubacterial equivalents on the polypeptide sequence level. All the analyzed genes are preceded by ribosome binding sites of eubacterial type. In addition to known putative promoter sequences, conserved structural elements of the DNA were detected surrounding the transcription initiation sites of the mcr genes.
对包含结构基因mcrA、mcrB、mcrC、mcrD和mcrG的共转录基因簇在三种产甲烷菌中进行了比较分析。mcrA、mcrB和mcrG是甲基辅酶M还原酶三个亚基的结构基因,而另外两个基因编码功能未知的多肽。产甲烷菌不同物种间mcr基因产物的保守程度各不相同。在不同细菌中,同源基因的G+C含量与其产物氨基酸序列的保守性之间未发现相关性。将嗜热自养甲烷杆菌的RNA聚合酶核心亚基基因作为进化标记,与大肠杆菌、酿酒酵母和黑腹果蝇中的对应基因进行比较,结果表明同源多肽结构域由不同数量的基因编码,这表明在进化过程中相邻基因发生了基因融合。在多肽序列水平上,古细菌亚基与其真核生物对应亚基的同源性比与真细菌对应亚基的同源性要强得多。所有分析的基因之前都有细菌类型的核糖体结合位点。除了已知的假定启动子序列外,在mcr基因转录起始位点周围还检测到了DNA的保守结构元件。