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Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case

BACKGROUND: In understanding the evolutionary process of vertebrates, cyclostomes (hagfishes and lamprey) occupy crucial positions. Resolving molecular phylogenetic relationships of cyclostome genes with gnathostomes (jawed vertebrates) genes is indispensable in deciphering both the species tree and...

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Autores principales: Qiu, Huan, Hildebrand, Falk, Kuraku, Shigehiro, Meyer, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141671/
https://www.ncbi.nlm.nih.gov/pubmed/21699680
http://dx.doi.org/10.1186/1471-2164-12-325
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author Qiu, Huan
Hildebrand, Falk
Kuraku, Shigehiro
Meyer, Axel
author_facet Qiu, Huan
Hildebrand, Falk
Kuraku, Shigehiro
Meyer, Axel
author_sort Qiu, Huan
collection PubMed
description BACKGROUND: In understanding the evolutionary process of vertebrates, cyclostomes (hagfishes and lamprey) occupy crucial positions. Resolving molecular phylogenetic relationships of cyclostome genes with gnathostomes (jawed vertebrates) genes is indispensable in deciphering both the species tree and gene trees. However, molecular phylogenetic analyses, especially those including lamprey genes, have produced highly discordant results between gene families. To efficiently scrutinize this problem using partial genome assemblies of early vertebrates, we focused on the potassium voltage-gated channel, shaker-related (KCNA) family, whose members are mostly single-exon. RESULTS: Seven sea lamprey KCNA genes as well as six elephant shark genes were identified, and their orthologies to bony vertebrate subgroups were assessed. In contrast to robustly supported orthology of the elephant shark genes to gnathostome subgroups, clear orthology of any sea lamprey gene could not be established. Notably, sea lamprey KCNA sequences displayed unique codon usage pattern and amino acid composition, probably associated with exceptionally high GC-content in their coding regions. This lamprey-specific property of coding sequences was also observed generally for genes outside this gene family. CONCLUSIONS: Our results suggest that secondary modifications of sequence properties unique to the lamprey lineage may be one of the factors preventing robust orthology assessments of lamprey genes, which deserves further genome-wide validation. The lamprey lineage-specific alteration of protein-coding sequence properties needs to be taken into consideration in tackling the key questions about early vertebrate evolution.
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spelling pubmed-31416712011-07-23 Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case Qiu, Huan Hildebrand, Falk Kuraku, Shigehiro Meyer, Axel BMC Genomics Research Article BACKGROUND: In understanding the evolutionary process of vertebrates, cyclostomes (hagfishes and lamprey) occupy crucial positions. Resolving molecular phylogenetic relationships of cyclostome genes with gnathostomes (jawed vertebrates) genes is indispensable in deciphering both the species tree and gene trees. However, molecular phylogenetic analyses, especially those including lamprey genes, have produced highly discordant results between gene families. To efficiently scrutinize this problem using partial genome assemblies of early vertebrates, we focused on the potassium voltage-gated channel, shaker-related (KCNA) family, whose members are mostly single-exon. RESULTS: Seven sea lamprey KCNA genes as well as six elephant shark genes were identified, and their orthologies to bony vertebrate subgroups were assessed. In contrast to robustly supported orthology of the elephant shark genes to gnathostome subgroups, clear orthology of any sea lamprey gene could not be established. Notably, sea lamprey KCNA sequences displayed unique codon usage pattern and amino acid composition, probably associated with exceptionally high GC-content in their coding regions. This lamprey-specific property of coding sequences was also observed generally for genes outside this gene family. CONCLUSIONS: Our results suggest that secondary modifications of sequence properties unique to the lamprey lineage may be one of the factors preventing robust orthology assessments of lamprey genes, which deserves further genome-wide validation. The lamprey lineage-specific alteration of protein-coding sequence properties needs to be taken into consideration in tackling the key questions about early vertebrate evolution. BioMed Central 2011-06-23 /pmc/articles/PMC3141671/ /pubmed/21699680 http://dx.doi.org/10.1186/1471-2164-12-325 Text en Copyright ©2011 Qiu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Qiu, Huan
Hildebrand, Falk
Kuraku, Shigehiro
Meyer, Axel
Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case
title Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case
title_full Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case
title_fullStr Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case
title_full_unstemmed Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case
title_short Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case
title_sort unresolved orthology and peculiar coding sequence properties of lamprey genes: the kcna gene family as test case
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141671/
https://www.ncbi.nlm.nih.gov/pubmed/21699680
http://dx.doi.org/10.1186/1471-2164-12-325
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