Convergent Evolution of Hemoglobin Function in High-Altitude Andean Waterfowl Involves Limited Parallelism at the Molecular Sequence Level
A fundamental question in evolutionary genetics concerns the extent to which adaptive phenotypic convergence is attributable to convergent or parallel changes at the molecular sequence level. Here we report a comparative analysis of hemoglobin (Hb) function in eight phylogenetically replicated pairs...
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description | A fundamental question in evolutionary genetics concerns the extent to which adaptive phenotypic convergence is attributable to convergent or parallel changes at the molecular sequence level. Here we report a comparative analysis of hemoglobin (Hb) function in eight phylogenetically replicated pairs of high- and low-altitude waterfowl taxa to test for convergence in the oxygenation properties of Hb, and to assess the extent to which convergence in biochemical phenotype is attributable to repeated amino acid replacements. Functional experiments on native Hb variants and protein engineering experiments based on site-directed mutagenesis revealed the phenotypic effects of specific amino acid replacements that were responsible for convergent increases in Hb-O2 affinity in multiple high-altitude taxa. In six of the eight taxon pairs, high-altitude taxa evolved derived increases in Hb-O2 affinity that were caused by a combination of unique replacements, parallel replacements (involving identical-by-state variants with independent mutational origins in different lineages), and collateral replacements (involving shared, identical-by-descent variants derived via introgressive hybridization). In genome scans of nucleotide differentiation involving high- and low-altitude populations of three separate species, function-altering amino acid polymorphisms in the globin genes emerged as highly significant outliers, providing independent evidence for adaptive divergence in Hb function. The experimental results demonstrate that convergent changes in protein function can occur through multiple historical paths, and can involve multiple possible mutations. Most cases of convergence in Hb function did not involve parallel substitutions and most parallel substitutions did not affect Hb-O2 affinity, indicating that the repeatability of phenotypic evolution does not require parallelism at the molecular level. |
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Here we report a comparative analysis of hemoglobin (Hb) function in eight phylogenetically replicated pairs of high- and low-altitude waterfowl taxa to test for convergence in the oxygenation properties of Hb, and to assess the extent to which convergence in biochemical phenotype is attributable to repeated amino acid replacements. Functional experiments on native Hb variants and protein engineering experiments based on site-directed mutagenesis revealed the phenotypic effects of specific amino acid replacements that were responsible for convergent increases in Hb-O2 affinity in multiple high-altitude taxa. In six of the eight taxon pairs, high-altitude taxa evolved derived increases in Hb-O2 affinity that were caused by a combination of unique replacements, parallel replacements (involving identical-by-state variants with independent mutational origins in different lineages), and collateral replacements (involving shared, identical-by-descent variants derived via introgressive hybridization). In genome scans of nucleotide differentiation involving high- and low-altitude populations of three separate species, function-altering amino acid polymorphisms in the globin genes emerged as highly significant outliers, providing independent evidence for adaptive divergence in Hb function. The experimental results demonstrate that convergent changes in protein function can occur through multiple historical paths, and can involve multiple possible mutations. Most cases of convergence in Hb function did not involve parallel substitutions and most parallel substitutions did not affect Hb-O2 affinity, indicating that the repeatability of phenotypic evolution does not require parallelism at the molecular level.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1005681</identifier><identifier>PMID: 26637114</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adaptation, Physiological - genetics ; alpha-Globins - chemistry ; alpha-Globins - genetics ; alpha-Globins - metabolism ; Altitude ; Animals ; beta-Globins - chemistry ; beta-Globins - genetics ; beta-Globins - metabolism ; Birds - blood ; Birds - genetics ; Birds - physiology ; Blood ; DNA sequencing ; Evolution & development ; Evolution, Molecular ; Experiments ; Genetic aspects ; Genotype & phenotype ; Hemoglobin ; Hemoglobins - chemistry ; Hemoglobins - genetics ; Methods ; Nucleotide sequencing ; Oxygen - metabolism ; Phenotype ; Phylogeny ; Polymorphism, Genetic ; Proteins ; Sequence Analysis, DNA ; Studies ; Waterfowl</subject><ispartof>PLoS genetics, 2015-12, Vol.11 (12), p.e1005681</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Natarajan et al 2015 Natarajan et al</rights><rights>2015 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Natarajan C, Projecto-Garcia J, Moriyama H, Weber RE, Muñoz-Fuentes V, Green AJ, et al. (2015) Convergent Evolution of Hemoglobin Function in High-Altitude Andean Waterfowl Involves Limited Parallelism at the Molecular Sequence Level. 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Here we report a comparative analysis of hemoglobin (Hb) function in eight phylogenetically replicated pairs of high- and low-altitude waterfowl taxa to test for convergence in the oxygenation properties of Hb, and to assess the extent to which convergence in biochemical phenotype is attributable to repeated amino acid replacements. Functional experiments on native Hb variants and protein engineering experiments based on site-directed mutagenesis revealed the phenotypic effects of specific amino acid replacements that were responsible for convergent increases in Hb-O2 affinity in multiple high-altitude taxa. In six of the eight taxon pairs, high-altitude taxa evolved derived increases in Hb-O2 affinity that were caused by a combination of unique replacements, parallel replacements (involving identical-by-state variants with independent mutational origins in different lineages), and collateral replacements (involving shared, identical-by-descent variants derived via introgressive hybridization). In genome scans of nucleotide differentiation involving high- and low-altitude populations of three separate species, function-altering amino acid polymorphisms in the globin genes emerged as highly significant outliers, providing independent evidence for adaptive divergence in Hb function. The experimental results demonstrate that convergent changes in protein function can occur through multiple historical paths, and can involve multiple possible mutations. Most cases of convergence in Hb function did not involve parallel substitutions and most parallel substitutions did not affect Hb-O2 affinity, indicating that the repeatability of phenotypic evolution does not require parallelism at the molecular level.</description><subject>Adaptation, Physiological - genetics</subject><subject>alpha-Globins - chemistry</subject><subject>alpha-Globins - genetics</subject><subject>alpha-Globins - metabolism</subject><subject>Altitude</subject><subject>Animals</subject><subject>beta-Globins - chemistry</subject><subject>beta-Globins - genetics</subject><subject>beta-Globins - metabolism</subject><subject>Birds - blood</subject><subject>Birds - genetics</subject><subject>Birds - physiology</subject><subject>Blood</subject><subject>DNA sequencing</subject><subject>Evolution & development</subject><subject>Evolution, Molecular</subject><subject>Experiments</subject><subject>Genetic aspects</subject><subject>Genotype & phenotype</subject><subject>Hemoglobin</subject><subject>Hemoglobins - chemistry</subject><subject>Hemoglobins - genetics</subject><subject>Methods</subject><subject>Nucleotide sequencing</subject><subject>Oxygen - metabolism</subject><subject>Phenotype</subject><subject>Phylogeny</subject><subject>Polymorphism, Genetic</subject><subject>Proteins</subject><subject>Sequence Analysis, DNA</subject><subject>Studies</subject><subject>Waterfowl</subject><issn>1553-7404</issn><issn>1553-7390</issn><issn>1553-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVk11v0zAUhiMEYqPwDxBYQkLiosWO87WbSVW10UqFIcbHpXXiHKeuHLvEToG_wK_GW7uplbgA5SLWyXMeR699kuQ5oxPGS_Z27YbegplsWrQTRmleVOxBcsrynI_LjGYPD9YnyRPv15TyvDorHycnaVFEBctOk98zZ7fYR0cgF1tnhqCdJU6ROXauNa7WllwOVt6W43qu29V4aoIOQ4NkahsES75BwF65H4YsbHRs0ZOl7nTAhnyEHoxBo31HIJCwQvLeGZSDgZ5c4_cBrUSyxC2ap8kjBcbjs_17lHy5vPg8m4-XV-8Ws-lyLMsiC-OqUWkpC6UyxaqmQgCOqmApz4taKpkWleKKYprzGiRwKnlVA2RY1_IsTzPKR8nLnXdjnBf7GL1g0c5LWjAeicWOaBysxabXHfS_hAMtbguubwX0QUuDIk1zJc_Kpok_kJVYA1LeKFUUkkMOUEbX-X63oe6wkTHomMiR9PiL1SvRuq3IipKmlEXBq52ghbiftspFTHbaSzHNcpZzWsZjHiWTv1DxabDT0llUOtaPGt4cNUQm4M_QwuC9WFx_-g_2w7-zV1-P2dcH7ArBhJXf30F_DGY7UPbO-x7VfX6MiptpuDtGcTMNYj8Nse3FYfb3TXfXn_8BnnYIUQ</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Natarajan, Chandrasekhar</creator><creator>Projecto-Garcia, Joana</creator><creator>Moriyama, Hideaki</creator><creator>Weber, Roy E</creator><creator>Muñoz-Fuentes, Violeta</creator><creator>Green, Andy J</creator><creator>Kopuchian, Cecilia</creator><creator>Tubaro, Pablo L</creator><creator>Alza, Luis</creator><creator>Bulgarella, Mariana</creator><creator>Smith, Matthew M</creator><creator>Wilson, Robert E</creator><creator>Fago, Angela</creator><creator>McCracken, Kevin G</creator><creator>Storz, Jay F</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20151201</creationdate><title>Convergent Evolution of Hemoglobin Function in High-Altitude Andean Waterfowl Involves Limited Parallelism at the Molecular Sequence Level</title><author>Natarajan, Chandrasekhar ; Projecto-Garcia, Joana ; Moriyama, Hideaki ; Weber, Roy E ; Muñoz-Fuentes, Violeta ; Green, Andy J ; Kopuchian, Cecilia ; Tubaro, Pablo L ; Alza, Luis ; Bulgarella, Mariana ; Smith, Matthew M ; Wilson, Robert E ; Fago, Angela ; McCracken, Kevin G ; Storz, Jay F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c764t-8df27c6ff4f18d8eaa3ef612356bcfc268f3f0e253baca30c38baa4ebbc952403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adaptation, Physiological - genetics</topic><topic>alpha-Globins - chemistry</topic><topic>alpha-Globins - genetics</topic><topic>alpha-Globins - metabolism</topic><topic>Altitude</topic><topic>Animals</topic><topic>beta-Globins - chemistry</topic><topic>beta-Globins - genetics</topic><topic>beta-Globins - metabolism</topic><topic>Birds - blood</topic><topic>Birds - genetics</topic><topic>Birds - physiology</topic><topic>Blood</topic><topic>DNA sequencing</topic><topic>Evolution & development</topic><topic>Evolution, Molecular</topic><topic>Experiments</topic><topic>Genetic aspects</topic><topic>Genotype & phenotype</topic><topic>Hemoglobin</topic><topic>Hemoglobins - chemistry</topic><topic>Hemoglobins - genetics</topic><topic>Methods</topic><topic>Nucleotide sequencing</topic><topic>Oxygen - metabolism</topic><topic>Phenotype</topic><topic>Phylogeny</topic><topic>Polymorphism, Genetic</topic><topic>Proteins</topic><topic>Sequence Analysis, DNA</topic><topic>Studies</topic><topic>Waterfowl</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Natarajan, Chandrasekhar</creatorcontrib><creatorcontrib>Projecto-Garcia, Joana</creatorcontrib><creatorcontrib>Moriyama, Hideaki</creatorcontrib><creatorcontrib>Weber, Roy E</creatorcontrib><creatorcontrib>Muñoz-Fuentes, Violeta</creatorcontrib><creatorcontrib>Green, Andy J</creatorcontrib><creatorcontrib>Kopuchian, Cecilia</creatorcontrib><creatorcontrib>Tubaro, Pablo L</creatorcontrib><creatorcontrib>Alza, Luis</creatorcontrib><creatorcontrib>Bulgarella, Mariana</creatorcontrib><creatorcontrib>Smith, Matthew M</creatorcontrib><creatorcontrib>Wilson, Robert E</creatorcontrib><creatorcontrib>Fago, Angela</creatorcontrib><creatorcontrib>McCracken, Kevin G</creatorcontrib><creatorcontrib>Storz, Jay F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Natarajan, Chandrasekhar</au><au>Projecto-Garcia, Joana</au><au>Moriyama, Hideaki</au><au>Weber, Roy E</au><au>Muñoz-Fuentes, Violeta</au><au>Green, Andy J</au><au>Kopuchian, Cecilia</au><au>Tubaro, Pablo L</au><au>Alza, Luis</au><au>Bulgarella, Mariana</au><au>Smith, Matthew M</au><au>Wilson, Robert E</au><au>Fago, Angela</au><au>McCracken, Kevin G</au><au>Storz, Jay F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convergent Evolution of Hemoglobin Function in High-Altitude Andean Waterfowl Involves Limited Parallelism at the Molecular Sequence Level</atitle><jtitle>PLoS genetics</jtitle><addtitle>PLoS Genet</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>11</volume><issue>12</issue><spage>e1005681</spage><pages>e1005681-</pages><issn>1553-7404</issn><issn>1553-7390</issn><eissn>1553-7404</eissn><abstract>A fundamental question in evolutionary genetics concerns the extent to which adaptive phenotypic convergence is attributable to convergent or parallel changes at the molecular sequence level. Here we report a comparative analysis of hemoglobin (Hb) function in eight phylogenetically replicated pairs of high- and low-altitude waterfowl taxa to test for convergence in the oxygenation properties of Hb, and to assess the extent to which convergence in biochemical phenotype is attributable to repeated amino acid replacements. Functional experiments on native Hb variants and protein engineering experiments based on site-directed mutagenesis revealed the phenotypic effects of specific amino acid replacements that were responsible for convergent increases in Hb-O2 affinity in multiple high-altitude taxa. In six of the eight taxon pairs, high-altitude taxa evolved derived increases in Hb-O2 affinity that were caused by a combination of unique replacements, parallel replacements (involving identical-by-state variants with independent mutational origins in different lineages), and collateral replacements (involving shared, identical-by-descent variants derived via introgressive hybridization). In genome scans of nucleotide differentiation involving high- and low-altitude populations of three separate species, function-altering amino acid polymorphisms in the globin genes emerged as highly significant outliers, providing independent evidence for adaptive divergence in Hb function. The experimental results demonstrate that convergent changes in protein function can occur through multiple historical paths, and can involve multiple possible mutations. Most cases of convergence in Hb function did not involve parallel substitutions and most parallel substitutions did not affect Hb-O2 affinity, indicating that the repeatability of phenotypic evolution does not require parallelism at the molecular level.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26637114</pmid><doi>10.1371/journal.pgen.1005681</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation, Physiological - genetics alpha-Globins - chemistry alpha-Globins - genetics alpha-Globins - metabolism Altitude Animals beta-Globins - chemistry beta-Globins - genetics beta-Globins - metabolism Birds - blood Birds - genetics Birds - physiology Blood DNA sequencing Evolution & development Evolution, Molecular Experiments Genetic aspects Genotype & phenotype Hemoglobin Hemoglobins - chemistry Hemoglobins - genetics Methods Nucleotide sequencing Oxygen - metabolism Phenotype Phylogeny Polymorphism, Genetic Proteins Sequence Analysis, DNA Studies Waterfowl |
title | Convergent Evolution of Hemoglobin Function in High-Altitude Andean Waterfowl Involves Limited Parallelism at the Molecular Sequence Level |
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