Literature DB >> 16713575

In vivo molecular evolution reveals biophysical origins of organismal fitness.

Rafael Couñago1, Stephen Chen, Yousif Shamoo.   

Abstract

In nature, evolution occurs through the continuous adaptation of a population to its environment. At the molecular level, adaptive changes in protein sequence and expression impact organismal fitness and, consequently, dictate population dynamics. Here, we have used a "weak link" method to favor variations in one gene, allowing adaptation to thermostability to be studied in molecular detail as bacteria were grown continuously for approximately 1500 generations. Surprisingly, only six mutant alleles, representing less than 1% of the possible missense mutations, were observed, suggesting a highly constrained molecular landscape during protein evolution. The changes in organismal fitness were linked directly to incremental increases in enzyme stability and activity maxima and corresponded to the narrow temperature ranges where each mutant enjoyed success within the overall population. Thus, continuous evolution of a single gene permits a quantitative approach that extends from the phenotypes of the microbial populations to their underlying biophysical basis.

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Year:  2006        PMID: 16713575     DOI: 10.1016/j.molcel.2006.04.012

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  50 in total

1.  Experimental evolution of adenylate kinase reveals contrasting strategies toward protein thermostability.

Authors:  Corwin Miller; Milya Davlieva; Corey Wilson; Kristopher I White; Rafael Couñago; Gang Wu; Jeffrey C Myers; Pernilla Wittung-Stafshede; Yousif Shamoo
Journal:  Biophys J       Date:  2010-08-04       Impact factor: 4.033

2.  Thermal adaptation of viruses and bacteria.

Authors:  Peiqiu Chen; Eugene I Shakhnovich
Journal:  Biophys J       Date:  2010-04-07       Impact factor: 4.033

3.  Evolution of a single gene highlights the complexity underlying molecular descriptions of fitness.

Authors:  Matthew I Peña; Elizabeth Van Itallie; Matthew R Bennett; Yousif Shamoo
Journal:  Chaos       Date:  2010-06       Impact factor: 3.642

4.  How mutational epistasis impairs predictability in protein evolution and design.

Authors:  Charlotte M Miton; Nobuhiko Tokuriki
Journal:  Protein Sci       Date:  2016-01-22       Impact factor: 6.725

5.  Thermostability/infectivity defect caused by deletion of the core protein V gene in human adenovirus type 5 is rescued by thermo-selectable mutations in the core protein X precursor.

Authors:  Hideyo Ugai; Anton V Borovjagin; Long P Le; Minghui Wang; David T Curiel
Journal:  J Mol Biol       Date:  2006-12-06       Impact factor: 5.469

Review 6.  Genetic constraints on protein evolution.

Authors:  Manel Camps; Asael Herman; Ern Loh; Lawrence A Loeb
Journal:  Crit Rev Biochem Mol Biol       Date:  2007 Sep-Oct       Impact factor: 8.250

7.  Bioinformatic method for protein thermal stabilization by structural entropy optimization.

Authors:  Euiyoung Bae; Ryan M Bannen; George N Phillips
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-08       Impact factor: 11.205

8.  Lethal mutagenesis in viruses and bacteria.

Authors:  Peiqiu Chen; Eugene I Shakhnovich
Journal:  Genetics       Date:  2009-07-20       Impact factor: 4.562

9.  Zipping and unzipping of adenylate kinase: atomistic insights into the ensemble of open<-->closed transitions.

Authors:  Oliver Beckstein; Elizabeth J Denning; Juan R Perilla; Thomas B Woolf
Journal:  J Mol Biol       Date:  2009-09-12       Impact factor: 5.469

10.  Functional and metabolic effects of adaptive glycerol kinase (GLPK) mutants in Escherichia coli.

Authors:  M Kenyon Applebee; Andrew R Joyce; Tom M Conrad; Donald W Pettigrew; Bernhard Ø Palsson
Journal:  J Biol Chem       Date:  2011-05-06       Impact factor: 5.157

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