Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages

<p>Abstract</p> <p>Background</p> <p>Gene duplication provides opportunities for lineage diversification and evolution of developmental novelties. Duplicated genes generally either disappear by accumulation of mutations (nonfunctionalization), or are preserved either by...

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Main Authors: Cañestro Cristian, Bassham Susan, Postlethwait John H
Format: Article
Language:English
Published: BMC 2008-08-01
Series:BMC Biology
Online Access:http://www.biomedcentral.com/1741-7007/6/35
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spelling doaj-97fbbfec38f640028931a767543e3a492020-11-25T00:37:53ZengBMCBMC Biology1741-70072008-08-01613510.1186/1741-7007-6-35Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineagesCañestro CristianBassham SusanPostlethwait John H<p>Abstract</p> <p>Background</p> <p>Gene duplication provides opportunities for lineage diversification and evolution of developmental novelties. Duplicated genes generally either disappear by accumulation of mutations (nonfunctionalization), or are preserved either by the origin of positively selected functions in one or both duplicates (neofunctionalization), or by the partitioning of original gene subfunctions between the duplicates (subfunctionalization). The Pax2/5/8 family of important developmental regulators has undergone parallel expansion among chordate groups. After the divergence of urochordate and vertebrate lineages, two rounds of independent gene duplications resulted in the <it>Pax2, Pax5</it>, and <it>Pax8 </it>genes of most vertebrates (the sister group of the urochordates), and an additional duplication provided the <it>pax2a </it>and <it>pax2b </it>duplicates in teleost fish. Separate from the vertebrate genome expansions, a duplication also created two <it>Pax2/5/8 </it>genes in the common ancestor of ascidian and larvacean urochordates.</p> <p>Results</p> <p>To better understand mechanisms underlying the evolution of duplicated genes, we investigated, in the larvacean urochordate <it>Oikopleura dioica</it>, the embryonic gene expression patterns of <it>Pax2/5/8 </it>paralogs. We compared the larvacean and ascidian expression patterns to infer modular subfunctions present in the single pre-duplication <it>Pax2/5/8 </it>gene of stem urochordates, and we compared vertebrate and urochordate expression to infer the suite of <it>Pax2/5/8 </it>gene subfunctions in the common ancestor of olfactores (vertebrates + urochordates). Expression pattern differences of larvacean and ascidian Pax2/5/8 orthologs in the endostyle, pharynx and hindgut suggest that some ancestral gene functions have been partitioned differently to the duplicates in the two urochordate lineages. Novel expression in the larvacean heart may have resulted from the neofunctionalization of a <it>Pax2/5/8 </it>gene in the urochordates. Expression of larvacean <it>Pax2/5/8 </it>in the endostyle, in sites of epithelial remodeling, and in sensory tissues evokes like functions of <it>Pax2</it>, <it>Pax5 </it>and <it>Pax8 </it>in vertebrate embryos, and may indicate ancient origins for these functions in the chordate common ancestor.</p> <p>Conclusion</p> <p>Comparative analysis of expression patterns of chordate Pax2/5/8 duplicates, rooted on the single-copy <it>Pax2/5/8 </it>gene of amphioxus, whose lineage diverged basally among chordates, provides new insights into the evolution and development of the heart, thyroid, pharynx, stomodeum and placodes in chordates; supports the controversial conclusion that the atrial siphon of ascidians and the otic placode in vertebrates are homologous; and backs the notion that <it>Pax2/5/8 </it>functioned in ancestral chordates to engineer epithelial fusions and perforations, including gill slit openings.</p> http://www.biomedcentral.com/1741-7007/6/35
collection DOAJ
language English
format Article
sources DOAJ
author Cañestro Cristian
Bassham Susan
Postlethwait John H
spellingShingle Cañestro Cristian
Bassham Susan
Postlethwait John H
Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages
BMC Biology
author_facet Cañestro Cristian
Bassham Susan
Postlethwait John H
author_sort Cañestro Cristian
title Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages
title_short Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages
title_full Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages
title_fullStr Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages
title_full_unstemmed Evolution of developmental roles of <it>Pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages
title_sort evolution of developmental roles of <it>pax2/5/8 </it>paralogs after independent duplication in urochordate and vertebrate lineages
publisher BMC
series BMC Biology
issn 1741-7007
publishDate 2008-08-01
description <p>Abstract</p> <p>Background</p> <p>Gene duplication provides opportunities for lineage diversification and evolution of developmental novelties. Duplicated genes generally either disappear by accumulation of mutations (nonfunctionalization), or are preserved either by the origin of positively selected functions in one or both duplicates (neofunctionalization), or by the partitioning of original gene subfunctions between the duplicates (subfunctionalization). The Pax2/5/8 family of important developmental regulators has undergone parallel expansion among chordate groups. After the divergence of urochordate and vertebrate lineages, two rounds of independent gene duplications resulted in the <it>Pax2, Pax5</it>, and <it>Pax8 </it>genes of most vertebrates (the sister group of the urochordates), and an additional duplication provided the <it>pax2a </it>and <it>pax2b </it>duplicates in teleost fish. Separate from the vertebrate genome expansions, a duplication also created two <it>Pax2/5/8 </it>genes in the common ancestor of ascidian and larvacean urochordates.</p> <p>Results</p> <p>To better understand mechanisms underlying the evolution of duplicated genes, we investigated, in the larvacean urochordate <it>Oikopleura dioica</it>, the embryonic gene expression patterns of <it>Pax2/5/8 </it>paralogs. We compared the larvacean and ascidian expression patterns to infer modular subfunctions present in the single pre-duplication <it>Pax2/5/8 </it>gene of stem urochordates, and we compared vertebrate and urochordate expression to infer the suite of <it>Pax2/5/8 </it>gene subfunctions in the common ancestor of olfactores (vertebrates + urochordates). Expression pattern differences of larvacean and ascidian Pax2/5/8 orthologs in the endostyle, pharynx and hindgut suggest that some ancestral gene functions have been partitioned differently to the duplicates in the two urochordate lineages. Novel expression in the larvacean heart may have resulted from the neofunctionalization of a <it>Pax2/5/8 </it>gene in the urochordates. Expression of larvacean <it>Pax2/5/8 </it>in the endostyle, in sites of epithelial remodeling, and in sensory tissues evokes like functions of <it>Pax2</it>, <it>Pax5 </it>and <it>Pax8 </it>in vertebrate embryos, and may indicate ancient origins for these functions in the chordate common ancestor.</p> <p>Conclusion</p> <p>Comparative analysis of expression patterns of chordate Pax2/5/8 duplicates, rooted on the single-copy <it>Pax2/5/8 </it>gene of amphioxus, whose lineage diverged basally among chordates, provides new insights into the evolution and development of the heart, thyroid, pharynx, stomodeum and placodes in chordates; supports the controversial conclusion that the atrial siphon of ascidians and the otic placode in vertebrates are homologous; and backs the notion that <it>Pax2/5/8 </it>functioned in ancestral chordates to engineer epithelial fusions and perforations, including gill slit openings.</p>
url http://www.biomedcentral.com/1741-7007/6/35
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