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Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes

BACKGROUND: Type II antifreeze protein (AFP) from the rainbow smelt, Osmerus mordax, is a calcium-dependent C-type lectin homolog, similar to the AFPs from herring and sea raven. While C-type lectins are ubiquitous, type II AFPs are only found in a few species in three widely separated branches of t...

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Autores principales: Graham, Laurie A, Li, Jieying, Davidson, William S, Davies, Peter L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499448/
https://www.ncbi.nlm.nih.gov/pubmed/23009612
http://dx.doi.org/10.1186/1471-2148-12-190
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author Graham, Laurie A
Li, Jieying
Davidson, William S
Davies, Peter L
author_facet Graham, Laurie A
Li, Jieying
Davidson, William S
Davies, Peter L
author_sort Graham, Laurie A
collection PubMed
description BACKGROUND: Type II antifreeze protein (AFP) from the rainbow smelt, Osmerus mordax, is a calcium-dependent C-type lectin homolog, similar to the AFPs from herring and sea raven. While C-type lectins are ubiquitous, type II AFPs are only found in a few species in three widely separated branches of teleost fishes. Furthermore, several other non-homologous AFPs are found in intervening species. We have previously postulated that this sporadic distribution has resulted from lateral gene transfer. The alternative hypothesis, that the AFP evolved from a lectin present in a shared ancestor and that this gene was lost in most species, is not favored because both the exon and intron sequences are highly conserved. RESULTS: Here we have sequenced and annotated a 160 kb smelt BAC clone containing a centrally-located AFP gene along with 14 other genes. Quantitative PCR indicates that there is but a single copy of this gene within the smelt genome, which is atypical for fish AFP genes. The corresponding syntenic region has been identified and searched in a number of other species and found to be devoid of lectin or AFP sequences. Unlike the introns of the AFP gene, the intronic sequences of the flanking genes are not conserved between species. As well, the rate and pattern of mutation in the AFP gene are radically different from those seen in other smelt and herring genes. CONCLUSIONS: These results provide stand-alone support for an example of lateral gene transfer between vertebrate species. They should further inform the debate about genetically modified organisms by showing that gene transfer between ‘higher’ eukaryotes can occur naturally. Analysis of the syntenic regions from several fishes strongly suggests that the smelt acquired the AFP gene from the herring.
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spelling pubmed-34994482012-11-16 Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes Graham, Laurie A Li, Jieying Davidson, William S Davies, Peter L BMC Evol Biol Research Article BACKGROUND: Type II antifreeze protein (AFP) from the rainbow smelt, Osmerus mordax, is a calcium-dependent C-type lectin homolog, similar to the AFPs from herring and sea raven. While C-type lectins are ubiquitous, type II AFPs are only found in a few species in three widely separated branches of teleost fishes. Furthermore, several other non-homologous AFPs are found in intervening species. We have previously postulated that this sporadic distribution has resulted from lateral gene transfer. The alternative hypothesis, that the AFP evolved from a lectin present in a shared ancestor and that this gene was lost in most species, is not favored because both the exon and intron sequences are highly conserved. RESULTS: Here we have sequenced and annotated a 160 kb smelt BAC clone containing a centrally-located AFP gene along with 14 other genes. Quantitative PCR indicates that there is but a single copy of this gene within the smelt genome, which is atypical for fish AFP genes. The corresponding syntenic region has been identified and searched in a number of other species and found to be devoid of lectin or AFP sequences. Unlike the introns of the AFP gene, the intronic sequences of the flanking genes are not conserved between species. As well, the rate and pattern of mutation in the AFP gene are radically different from those seen in other smelt and herring genes. CONCLUSIONS: These results provide stand-alone support for an example of lateral gene transfer between vertebrate species. They should further inform the debate about genetically modified organisms by showing that gene transfer between ‘higher’ eukaryotes can occur naturally. Analysis of the syntenic regions from several fishes strongly suggests that the smelt acquired the AFP gene from the herring. BioMed Central 2012-09-25 /pmc/articles/PMC3499448/ /pubmed/23009612 http://dx.doi.org/10.1186/1471-2148-12-190 Text en Copyright ©2012 Graham 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
Graham, Laurie A
Li, Jieying
Davidson, William S
Davies, Peter L
Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes
title Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes
title_full Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes
title_fullStr Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes
title_full_unstemmed Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes
title_short Smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes
title_sort smelt was the likely beneficiary of an antifreeze gene laterally transferred between fishes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499448/
https://www.ncbi.nlm.nih.gov/pubmed/23009612
http://dx.doi.org/10.1186/1471-2148-12-190
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