Literature DB >> 15986834

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

Radhey S Gupta1.   

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.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15986834     DOI: 10.1080/10408410590922393

Source DB:  PubMed          Journal:  Crit Rev Microbiol        ISSN: 1040-841X            Impact factor:   7.624


  20 in total

Review 1.  Molecular signatures for the main phyla of photosynthetic bacteria and their subgroups.

Authors:  Radhey S Gupta
Journal:  Photosynth Res       Date:  2010-04-23       Impact factor: 3.573

2.  Application of the character compatibility approach to generalized molecular sequence data: branching order of the proteobacterial subdivisions.

Authors:  Radhey S Gupta; Peter H A Sneath
Journal:  J Mol Evol       Date:  2006-12-09       Impact factor: 2.395

3.  A robust species tree for the alphaproteobacteria.

Authors:  Kelly P Williams; Bruno W Sobral; Allan W Dickerman
Journal:  J Bacteriol       Date:  2007-05-04       Impact factor: 3.490

4.  Viral distribution and life strategies in the Bach Dang Estuary, Vietnam.

Authors:  Yvan Bettarel; Thierry Bouvier; Martin Agis; Corinne Bouvier; Thuoc Van Chu; Marine Combe; Xavier Mari; Minh Ngoc Nghiem; Thuy Thanh Nguyen; Thu The Pham; Olivier Pringault; Emma Rochelle-Newall; Jean-Pascal Torréton; Huy Quang Tran
Journal:  Microb Ecol       Date:  2011-03-09       Impact factor: 4.552

5.  Discrete Responses to Limitation for Iron and Manganese in Agrobacterium tumefaciens: Influence on Attachment and Biofilm Formation.

Authors:  Jason E Heindl; Michael E Hibbing; Jing Xu; Ramya Natarajan; Aaron M Buechlein; Clay Fuqua
Journal:  J Bacteriol       Date:  2015-12-28       Impact factor: 3.490

6.  Cell cycle progression in Caulobacter requires a nucleoid-associated protein with high AT sequence recognition.

Authors:  Dante P Ricci; Michael D Melfi; Keren Lasker; David L Dill; Harley H McAdams; Lucy Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-19       Impact factor: 11.205

7.  The diversity and evolution of cell cycle regulation in alpha-proteobacteria: a comparative genomic analysis.

Authors:  Matteo Brilli; Marco Fondi; Renato Fani; Alessio Mengoni; Lorenzo Ferri; Marco Bazzicalupo; Emanuele G Biondi
Journal:  BMC Syst Biol       Date:  2010-04-28

Review 8.  A review of Brucella infection in marine mammals, with special emphasis on Brucella pinnipedialis in the hooded seal (Cystophora cristata).

Authors:  Ingebjørg H Nymo; Morten Tryland; Jacques Godfroid
Journal:  Vet Res       Date:  2011-08-05       Impact factor: 3.683

9.  Ancient Bacterial Class Alphaproteobacteria Cytochrome P450 Monooxygenases Can Be Found in Other Bacterial Species.

Authors:  Nomfundo Nzuza; Tiara Padayachee; Puleng Rosinah Syed; Justyna Dorota Kryś; Wanping Chen; Dominik Gront; David R Nelson; Khajamohiddin Syed
Journal:  Int J Mol Sci       Date:  2021-05-24       Impact factor: 5.923

10.  Meta-analysis of general bacterial subclades in whole-genome phylogenies using tree topology profiling.

Authors:  Thomas Meinel; Antje Krause
Journal:  Evol Bioinform Online       Date:  2012-08-07       Impact factor: 1.625

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.