Springer E, Sachs M S, Woese C R, Boone D R
Department of Environmental Science and Engineering, Oregon Graduate Institute of Science & Technology, Portland 97291-1000, USA.
Int J Syst Bacteriol. 1995 Jul;45(3):554-9. doi: 10.1099/00207713-45-3-554.
Representatives of the family Methanosarcinaceae were analyzed phylogenetically by comparing partial sequences of their methyl-coenzyme M reductase (mcrI) genes. A 490-bp fragment from the A subunit of the gene was selected, amplified by the PCR, cloned, and sequenced for each of 25 strains belonging to the Methanosarcinaceae. The sequences obtained were aligned with the corresponding portions of five previously published sequences, and all of the sequences were compared to determine phylogenetic distances by Fitch distance matrix methods. We prepared analogous trees based on 16S rRNA sequences; these trees corresponded closely to the mcrI trees, although the mcrI sequences of pairs of organisms had 3.01 +/- 0.541 times more changes than the respective pairs of 16S rRNA sequences, suggesting that the mcrI fragment evolved about three times more rapidly than the 16S rRNA gene. The qualitative similarity of the mcrI and 16S rRNA trees suggests that transfer of genetic information between dissimilar organisms has not significantly affected these sequences, although we found inconsistencies between some mcrI distances that we measured and and previously published DNA reassociation data. It is unlikely that multiple mcrI isogenes were present in the organisms that we examined, because we found no major discrepancies in multiple determinations of mcrI sequences from the same organism. Our primers for the PCR also match analogous sites in the previously published mcrII sequences, but all of the sequences that we obtained from members of the Methanosarcinaceae were more closely related to mcrI sequences than to mcrII sequences, suggesting that members of the Methanosarcinaceae do not have distinct mcrII genes.
通过比较甲烷八叠球菌科(Methanosarcinaceae)成员的甲基辅酶M还原酶(mcrI)基因的部分序列,对该科进行了系统发育分析。从该基因的A亚基中选取了一个490bp的片段,通过PCR进行扩增、克隆,并对属于甲烷八叠球菌科的25个菌株中的每一个进行测序。将获得的序列与之前发表的5个序列的相应部分进行比对,并通过菲奇距离矩阵法比较所有序列以确定系统发育距离。我们基于16S rRNA序列构建了类似的树;这些树与mcrI树密切对应,尽管成对生物体的mcrI序列的变化比相应的成对16S rRNA序列多3.01±0.541倍,这表明mcrI片段的进化速度比16S rRNA基因快约三倍。mcrI和16S rRNA树的定性相似性表明,不同生物体之间的遗传信息转移并未对这些序列产生显著影响,尽管我们发现我们测量的一些mcrI距离与之前发表的DNA重结合数据之间存在不一致。我们检测的生物体中不太可能存在多个mcrI同基因,因为我们从同一生物体的多次mcrI序列测定中未发现重大差异。我们用于PCR的引物也与之前发表的mcrII序列中的类似位点匹配,但我们从甲烷八叠球菌科成员获得的所有序列与mcrI序列的关系比与mcrII序列的关系更密切,这表明甲烷八叠球菌科成员没有明显的mcrII基因。