Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genes

<p>Abstract</p> <p>Background</p> <p>Gene duplication followed by functional divergence has long been hypothesized to be the main source of molecular novelty. Convincing examples of neofunctionalization, however, remain rare. Snake venom phospholipase A<sub>2 <...

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Main Author: Lynch Vincent J
Format: Article
Language:English
Published: BMC 2007-01-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/7/2
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spelling doaj-60a9ac7a4f7a4c2fb1c07ce1c702dba32021-09-02T14:38:56ZengBMCBMC Evolutionary Biology1471-21482007-01-0171210.1186/1471-2148-7-2Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genesLynch Vincent J<p>Abstract</p> <p>Background</p> <p>Gene duplication followed by functional divergence has long been hypothesized to be the main source of molecular novelty. Convincing examples of neofunctionalization, however, remain rare. Snake venom phospholipase A<sub>2 </sub>genes are members of large multigene families with many diverse functions, thus they are excellent models to study the emergence of novel functions after gene duplications.</p> <p>Results</p> <p>Here, I show that positive Darwinian selection and neofunctionalization is common in snake venom phospholipase A<sub>2 </sub>genes. The pattern of gene duplication and positive selection indicates that adaptive molecular evolution occurs immediately after duplication events as novel functions emerge and continues as gene families diversify and are refined. Surprisingly, adaptive evolution of group-I phospholipases in elapids is also associated with speciation events, suggesting adaptation of the phospholipase arsenal to novel prey species after niche shifts. Mapping the location of sites under positive selection onto the crystal structure of phospholipase A<sub>2 </sub>identified regions evolving under diversifying selection are located on the molecular surface and are likely protein-protein interactions sites essential for toxin functions.</p> <p>Conclusion</p> <p>These data show that increases in genomic complexity (through gene duplications) can lead to phenotypic complexity (venom composition) and that positive Darwinian selection is a common evolutionary force in snake venoms. Finally, regions identified under selection on the surface of phospholipase A<sub>2 </sub>enzymes are potential candidate sites for structure based antivenin design.</p> http://www.biomedcentral.com/1471-2148/7/2
collection DOAJ
language English
format Article
sources DOAJ
author Lynch Vincent J
spellingShingle Lynch Vincent J
Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genes
BMC Evolutionary Biology
author_facet Lynch Vincent J
author_sort Lynch Vincent J
title Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genes
title_short Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genes
title_full Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genes
title_fullStr Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genes
title_full_unstemmed Inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase A<sub>2 </sub>genes
title_sort inventing an arsenal: adaptive evolution and neofunctionalization of snake venom phospholipase a<sub>2 </sub>genes
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2007-01-01
description <p>Abstract</p> <p>Background</p> <p>Gene duplication followed by functional divergence has long been hypothesized to be the main source of molecular novelty. Convincing examples of neofunctionalization, however, remain rare. Snake venom phospholipase A<sub>2 </sub>genes are members of large multigene families with many diverse functions, thus they are excellent models to study the emergence of novel functions after gene duplications.</p> <p>Results</p> <p>Here, I show that positive Darwinian selection and neofunctionalization is common in snake venom phospholipase A<sub>2 </sub>genes. The pattern of gene duplication and positive selection indicates that adaptive molecular evolution occurs immediately after duplication events as novel functions emerge and continues as gene families diversify and are refined. Surprisingly, adaptive evolution of group-I phospholipases in elapids is also associated with speciation events, suggesting adaptation of the phospholipase arsenal to novel prey species after niche shifts. Mapping the location of sites under positive selection onto the crystal structure of phospholipase A<sub>2 </sub>identified regions evolving under diversifying selection are located on the molecular surface and are likely protein-protein interactions sites essential for toxin functions.</p> <p>Conclusion</p> <p>These data show that increases in genomic complexity (through gene duplications) can lead to phenotypic complexity (venom composition) and that positive Darwinian selection is a common evolutionary force in snake venoms. Finally, regions identified under selection on the surface of phospholipase A<sub>2 </sub>enzymes are potential candidate sites for structure based antivenin design.</p>
url http://www.biomedcentral.com/1471-2148/7/2
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