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α-变形菌纲及其亚群特有的蛋白质特征以及α-变形菌纲的进化模型。

Protein signatures distinctive of alpha proteobacteria and its subgroups and a model for alpha-proteobacterial evolution.

作者信息

Gupta Radhey S

机构信息

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.

出版信息

Crit Rev Microbiol. 2005;31(2):101-35. doi: 10.1080/10408410590922393.

Abstract

Alpha (alpha) proteobacteria comprise a large and metabolically diverse group. No biochemical or molecular feature is presently known that can distinguish these bacteria from other groups. The evolutionary relationships among this group, which includes numerous pathogens and agriculturally important microbes, are also not understood. Shared conserved inserts and deletions (i.e., indels or signatures) in molecular sequences provide a powerful means for identification of different groups in clear terms, and for evolutionary studies (see www.bacterialphylogeny.com). This review describes, for the first time, a large number of conserved indels in broadly distributed proteins that are distinctive and unifying characteristics of either all alpha-proteobacteria, or many of its constituent subgroups (i.e., orders, families, etc.). These signatures were identified by systematic analyses of proteins found in the Rickettsia prowazekii (RP) genome. Conserved indels that are unique to alpha-proteobacteria are present in the following proteins: Cytochrome c oxidase assembly protein Ctag, PurC, DnaB, ATP synthase alpha-subunit, exonuclease VII, prolipoprotein phosphatidylglycerol transferase, RP-400, FtsK, puruvate phosphate dikinase, cytochrome b, MutY, and homoserine dehydrogenase. The signatures in succinyl-CoA synthetase, cytochrome oxidase I, alanyl-tRNA synthetase, and MutS proteins are found in all alpha-proteobacteria, except the Rickettsiales, indicating that this group has diverged prior to the introduction of these signatures. A number of proteins contain conserved indels that are specific for Rickettsiales (XerD integrase and leucine aminopeptidase), Rickettsiaceae (Mfd, ribosomal protein L19, FtsZ, Sigma 70 and exonuclease VII), or Anaplasmataceae (Tgt and RP-314), and they distinguish these groups from all others. Signatures in DnaA, RP-057, and DNA ligase A are commonly shared by various Rhizobiales, Rhodobacterales, and Caulobacter, suggesting that these groups shared a common ancestor exclusive of other alpha-proteobacteria. A specific relationship between Rhodobacterales and Caulobacter is indicated by a large insert in the Asn-Gln amidotransferase. The Rhizobiales group of species are distinguished from others by a large insert in the Trp-tRNA synthetase. Signature sequences in a number of other proteins (viz. oxoglutarate dehydogenase, succinyl-CoA synthase, LytB, DNA gyrase A, LepA, and Ser-tRNA synthetase) serve to distinguish the Rhizobiaceae, Brucellaceae, and Phyllobacteriaceae families from Bradyrhizobiaceae and Methylobacteriaceae. Based on the distribution patterns of these signatures, it is now possible to logically deduce a model for the branching order among alpha-proteobacteria, which is as follows: Rickettsiales --> Rhodospirillales-Sphingomonadales --> Rhodobacterales-Caulobacterales --> Rhizobiales (Rhizobiaceaea-Brucellaceae-Phyllobacteriaceae, and Bradyrhizobiaceae). The deduced branching order is also consistent with the topologies in the 16 rRNA and other phylogenetic trees. Signature sequences in a number of other proteins provide evidence that alpha-proteobacteria is a late branching taxa within Bacteria, which branched after the delta,epsilon-subdivisions but prior to the beta,gamma-proteobacteria. The shared presence of many of these signatures in the mitochondrial (eukaryotic) homologs also provides evidence of the alpha-proteobacterial ancestry of mitochondria.

摘要

α-变形菌纲包含一个庞大且代谢多样的菌群。目前尚未发现能将这些细菌与其他菌群区分开来的生化或分子特征。该菌群包含众多病原体和具有农业重要性的微生物,其进化关系也尚不明确。分子序列中共享的保守插入和缺失(即插入缺失或特征序列)为明确鉴定不同菌群以及进行进化研究提供了有力手段(见www.bacterialphylogeny.com)。本综述首次描述了广泛分布的蛋白质中大量保守的插入缺失,这些是所有α-变形菌纲或其许多组成亚群(即目、科等)独特且统一的特征。这些特征序列是通过对普氏立克次体(RP)基因组中发现的蛋白质进行系统分析而确定的。α-变形菌纲特有的保守插入缺失存在于以下蛋白质中:细胞色素c氧化酶组装蛋白Ctag、PurC、DnaB、ATP合酶α亚基、核酸外切酶VII、前脂蛋白磷脂酰甘油转移酶、RP - 400、FtsK、丙酮酸磷酸二激酶、细胞色素b、MutY和高丝氨酸脱氢酶。琥珀酰辅酶A合成酶、细胞色素氧化酶I、丙氨酰 - tRNA合成酶和MutS蛋白中的特征序列存在于除立克次体目之外的所有α-变形菌纲中,这表明该目在这些特征序列出现之前就已分化。许多蛋白质含有特定于立克次体目(XerD整合酶和亮氨酸氨肽酶)、立克次体科(Mfd、核糖体蛋白L19、FtsZ、Sigma 70和核酸外切酶VII)或无形体科(Tgt和RP - 314)的保守插入缺失,它们将这些菌群与其他所有菌群区分开来。DnaA、RP - 057和DNA连接酶A中的特征序列为各种根瘤菌目、红杆菌目和柄杆菌属所共有,这表明这些菌群有一个排除其他α-变形菌纲的共同祖先。天冬酰胺 - 谷氨酰胺酰胺转移酶中的一个大插入片段表明红杆菌目和柄杆菌属之间存在特定关系。根瘤菌目物种通过色氨酸 - tRNA合成酶中的一个大插入片段与其他物种区分开来。许多其他蛋白质(如草酰戊二酸脱氢酶、琥珀酰辅酶A合成酶、LytB、DNA促旋酶A、LepA和丝氨酸 - tRNA合成酶)中的特征序列有助于将根瘤菌科、布鲁氏菌科和叶杆菌科与慢生根瘤菌科和甲基杆菌科区分开来。基于这些特征序列的分布模式,现在有可能合理推断出α-变形菌纲之间的分支顺序模型如下:立克次体目 --> 红螺菌目 - 鞘脂单胞菌目 --> 红杆菌目 - 柄杆菌目 --> 根瘤菌目(根瘤菌科 - 布鲁氏菌科 - 叶杆菌科,以及慢生根瘤菌科)。推断出的分支顺序也与16 rRNA和其他系统发育树的拓扑结构一致。许多其他蛋白质中的特征序列提供了证据,表明α-变形菌纲是细菌中较晚分支的类群,它在δ、ε亚群之后但在β、γ-变形菌纲之前分支。线粒体(真核生物)同源物中许多这些特征序列的共同存在也提供了线粒体起源于α-变形菌纲的证据。

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