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从延伸因子1α的蛋白质系统发育推断共生原生生物纤细前胃虫(修正:纤细迪纳氏虫)在白蚁黑胸散白蚁后肠中的系统发育位置

Phylogenetic position of symbiotic protist Dinenympha [correction of Dinemympha] exilis in the hindgut of the termite Reticulitermes speratus inferred from the protein phylogeny of elongation factor 1 alpha.

作者信息

Moriya S, Ohkuma M, Kudo T

机构信息

Laboratory of Microbiology, Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.

出版信息

Gene. 1998 Apr 14;210(2):221-7. doi: 10.1016/s0378-1119(98)00078-x.

DOI:10.1016/s0378-1119(98)00078-x
PMID:9573371
Abstract

The phylogenetic position of the symbiotic oxymonad Dinenympha exilis, found in the hindgut of the lower termite Reticulitermes speratus, was determined by analysis of translation elongation factor 1 alpha (EF-1 alpha). cDNA corresponding to a major part of the amino acid coding region of EF-1 alpha mRNA was amplified by the reverse transcription polymerase chain reaction (RT-PCR) method from total mRNA of termite hindgut microorganisms without cultivation. The product was cloned into a plasmid vector, pGEM-T, and the clones were isolated and sequenced. One of the EF-1 alpha clones isolated was assigned to the protist D. exilis by whole-cell in-situ hybridization using a specific oligonucleotide probe with enzymatic signal amplification. The deduced amino acid sequence was aligned with those of other eukaryotic and archaeabacterial EF-1 alpha s, and the phylogenetic relationships among early branching eukaryotes were inferred by using the distance matrix method and the maximum parsimony method. The phylogenetic analysis indicated that the D. exilis offshoot occurred before mitochondria-containing organisms and D. exilis branched out after the diplomonads clade. These results indicate that the oxymonad D. exilis is one of the early branching organisms and suggest that the oxymonads form a lineage independent of other early branching organisms.

摘要

在低等白蚁黄胸散白蚁(Reticulitermes speratus)后肠中发现的共生尖毛虫(Dinenympha exilis)的系统发育位置,是通过对翻译延伸因子1α(EF-1α)进行分析来确定的。对应于EF-1α mRNA氨基酸编码区主要部分的cDNA,采用逆转录聚合酶链反应(RT-PCR)方法,从未经培养的白蚁后肠微生物总mRNA中扩增得到。产物被克隆到质粒载体pGEM-T中,分离克隆并进行测序。通过使用带有酶促信号放大的特异性寡核苷酸探针进行全细胞原位杂交,将分离得到的一个EF-1α克隆鉴定为原生生物D. exilis。推导得到的氨基酸序列与其他真核生物和古细菌的EF-1α序列进行比对,并使用距离矩阵法和最大简约法推断早期分支真核生物之间的系统发育关系。系统发育分析表明,D. exilis分支出现在含线粒体生物之前,且D. exilis在双滴虫类分支之后分支出来。这些结果表明尖毛虫D. exilis是早期分支生物之一,并提示尖毛虫类形成了一个独立于其他早期分支生物的谱系。

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