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Enhanced cross-species utility of conserved microsatellite markers in shorebirds

BACKGROUND: Microsatellite markers are popular genetic markers frequently used in forensic biology. Despite their popularity, the characterisation of polymorphic microsatellite loci and development of suitable markers takes considerable effort. Newly-available genomic databases make it feasible to i...

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Autores principales: Küpper, Clemens, Burke, Terry, Székely, Tamás, Dawson, Deborah A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2588463/
https://www.ncbi.nlm.nih.gov/pubmed/18950482
http://dx.doi.org/10.1186/1471-2164-9-502
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author Küpper, Clemens
Burke, Terry
Székely, Tamás
Dawson, Deborah A
author_facet Küpper, Clemens
Burke, Terry
Székely, Tamás
Dawson, Deborah A
author_sort Küpper, Clemens
collection PubMed
description BACKGROUND: Microsatellite markers are popular genetic markers frequently used in forensic biology. Despite their popularity, the characterisation of polymorphic microsatellite loci and development of suitable markers takes considerable effort. Newly-available genomic databases make it feasible to identify conserved genetic markers. We examined the utility and characteristics of conserved microsatellite markers in Charadriiformes (plovers, sandpipers, gulls and auks). This order harbours many species with diverse breeding systems, life histories and extraordinary migration biology whose genetics warrant investigation. However, research has been largely restrained by the limited availability of genetic markers. To examine the utility of conserved microsatellite loci as genetic markers we collated a database of Charadriiformes microsatellites, searched for homologues in the chicken genome and tested conserved markers for amplification and polymorphism in a range of charadriiform species. RESULTS: Sixty-eight (42%) of 161 charadriiform microsatellite loci were assigned to a single location in the chicken genome based on their E-value. Fifty-five primers designed from conserved microsatellite loci with an E-value of E-10 or lower amplified across a wider range of charadriiform species than a control group of primers from ten anonymous microsatellite loci. Twenty-three of 24 examined conserved markers were polymorphic, each in on average 3 of 12 species tested. CONCLUSION: Genomic sequence databases are useful tools to identify conserved genetic markers including those located in non-coding regions. By maximising primer sequence similarity between source species and database species, markers can be further improved and provide additional markers to study the molecular ecology of populations of non-model organisms.
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spelling pubmed-25884632008-11-27 Enhanced cross-species utility of conserved microsatellite markers in shorebirds Küpper, Clemens Burke, Terry Székely, Tamás Dawson, Deborah A BMC Genomics Methodology Article BACKGROUND: Microsatellite markers are popular genetic markers frequently used in forensic biology. Despite their popularity, the characterisation of polymorphic microsatellite loci and development of suitable markers takes considerable effort. Newly-available genomic databases make it feasible to identify conserved genetic markers. We examined the utility and characteristics of conserved microsatellite markers in Charadriiformes (plovers, sandpipers, gulls and auks). This order harbours many species with diverse breeding systems, life histories and extraordinary migration biology whose genetics warrant investigation. However, research has been largely restrained by the limited availability of genetic markers. To examine the utility of conserved microsatellite loci as genetic markers we collated a database of Charadriiformes microsatellites, searched for homologues in the chicken genome and tested conserved markers for amplification and polymorphism in a range of charadriiform species. RESULTS: Sixty-eight (42%) of 161 charadriiform microsatellite loci were assigned to a single location in the chicken genome based on their E-value. Fifty-five primers designed from conserved microsatellite loci with an E-value of E-10 or lower amplified across a wider range of charadriiform species than a control group of primers from ten anonymous microsatellite loci. Twenty-three of 24 examined conserved markers were polymorphic, each in on average 3 of 12 species tested. CONCLUSION: Genomic sequence databases are useful tools to identify conserved genetic markers including those located in non-coding regions. By maximising primer sequence similarity between source species and database species, markers can be further improved and provide additional markers to study the molecular ecology of populations of non-model organisms. BioMed Central 2008-10-24 /pmc/articles/PMC2588463/ /pubmed/18950482 http://dx.doi.org/10.1186/1471-2164-9-502 Text en Copyright © 2008 Küpper 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 Methodology Article
Küpper, Clemens
Burke, Terry
Székely, Tamás
Dawson, Deborah A
Enhanced cross-species utility of conserved microsatellite markers in shorebirds
title Enhanced cross-species utility of conserved microsatellite markers in shorebirds
title_full Enhanced cross-species utility of conserved microsatellite markers in shorebirds
title_fullStr Enhanced cross-species utility of conserved microsatellite markers in shorebirds
title_full_unstemmed Enhanced cross-species utility of conserved microsatellite markers in shorebirds
title_short Enhanced cross-species utility of conserved microsatellite markers in shorebirds
title_sort enhanced cross-species utility of conserved microsatellite markers in shorebirds
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2588463/
https://www.ncbi.nlm.nih.gov/pubmed/18950482
http://dx.doi.org/10.1186/1471-2164-9-502
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