Literature DB >> 11319258

Patterns of temperature adaptation in proteins from the bacteria Deinococcus radiodurans and Thermus thermophilus.

J H McDonald1.   

Abstract

Asymmetrical patterns of amino acid substitution in proteins of organisms living at moderate and high temperatures (mesophiles and thermophiles, respectively) are generally taken to indicate selection favoring different amino acids at different temperatures due to their biochemical properties. If that were the case, comparisons of different pairs of mesophilic and thermophilic taxa would exhibit similar patterns of substitutional asymmetry. A previous comparison of mesophilic versus thermophilic Methanococcus with mesophilic versus thermophilic Bacillus revealed several pairs of amino acids for which one amino acid was favored in thermophilic Bacillus and the other was favored in thermophilic Methanococcus. Most of this could be explained by the higher G+C content of the DNA of thermophilic Bacillus, a phenomenon not seen in the Methanococcus comparison. Here, I compared the mesophilic bacterium Deinococcus radiodurans and its thermophilic relative Thermus thermophilus, which are similar in G+C content. Of the 190 pairs of amino acids, 83 exhibited significant substitutional asymmetry, consistent with the pervasive effects of selection. Most of these significantly asymmetrical pairs of amino acids were asymmetrical in the direction predicted from the Methanococcus data, consistent with thermal adaptation resulting from universal biochemical properties of the amino acids. However, 12 pairs of amino acids exhibited asymmetry significantly different from and in the opposite direction of that found in the Methanococcus comparison, and 21 pairs of amino acids exhibited asymmetry that was significantly different from that found in the Bacillus comparison and could not be explained by the greater G+C content in thermophilic Bacillus. This suggests that selection due to universal biochemical properties of the amino acids and differences in G+C content are not the only causes of substitutional asymmetry between mesophiles and thermophiles. Instead, selection on taxon-specific properties of amino acids, such as their metabolic cost, may play a role in causing asymmetrical patterns of substitution.

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Year:  2001        PMID: 11319258     DOI: 10.1093/oxfordjournals.molbev.a003856

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  20 in total

1.  Natural selection of more designable folds: a mechanism for thermophilic adaptation.

Authors:  Jeremy L England; Boris E Shakhnovich; Eugene I Shakhnovich
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-03       Impact factor: 11.205

2.  Amino acid compositional shifts during streptophyte transitions to terrestrial habitats.

Authors:  Richard W Jobson; Yin-Long Qiu
Journal:  J Mol Evol       Date:  2010-12-14       Impact factor: 2.395

3.  Selection on synthesis cost affects interprotein amino acid usage in all three domains of life.

Authors:  Jonathan Swire
Journal:  J Mol Evol       Date:  2007-05-02       Impact factor: 2.395

4.  Important role of hydrophobic interactions in high-pressure adaptation of proteins.

Authors:  D A Afonnikov; K E Medvedev; K V Gunbin; N A Kolchanov
Journal:  Dokl Biochem Biophys       Date:  2011-07-03       Impact factor: 0.788

5.  Phosphoproteomic analysis reveals the effects of PilF phosphorylation on type IV pilus and biofilm formation in Thermus thermophilus HB27.

Authors:  Wan-Ling Wu; Jiahn-Haur Liao; Guang-Huey Lin; Miao-Hsia Lin; Ying-Che Chang; Suh-Yuen Liang; Feng-Ling Yang; Kay-Hooi Khoo; Shih-Hsiung Wu
Journal:  Mol Cell Proteomics       Date:  2013-07-04       Impact factor: 5.911

6.  PROTS: a fragment based protein thermo-stability potential.

Authors:  Yunqi Li; Jian Zhang; David Tai; C Russell Middaugh; Yang Zhang; Jianwen Fang
Journal:  Proteins       Date:  2011-10-05

7.  Comparative complete genome sequence analysis of the amino acid replacements responsible for the thermostability of Corynebacterium efficiens.

Authors:  Yousuke Nishio; Yoji Nakamura; Yutaka Kawarabayasi; Yoshihiro Usuda; Eiichiro Kimura; Shinichi Sugimoto; Kazuhiko Matsui; Akihiko Yamagishi; Hisashi Kikuchi; Kazuho Ikeo; Takashi Gojobori
Journal:  Genome Res       Date:  2003-07       Impact factor: 9.043

8.  Temperature adaptation at homologous sites in proteins from nine thermophile-mesophile species pairs.

Authors:  John H McDonald
Journal:  Genome Biol Evol       Date:  2010-07-12       Impact factor: 3.416

9.  Molecular characterization of cold adaptation of membrane proteins in the Vibrionaceae core-genome.

Authors:  Tim Kahlke; Steinar Thorvaldsen
Journal:  PLoS One       Date:  2012-12-17       Impact factor: 3.240

10.  In silico classification of proteins from acidic and neutral cytoplasms.

Authors:  Yaping Fang; C Russell Middaugh; Jianwen Fang
Journal:  PLoS One       Date:  2012-09-26       Impact factor: 3.240

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