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Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus

The increased transcription of the Cyp6g1 gene of Drosophila melanogaster, and consequent resistance to insecticides such as DDT, is a widely cited example of adaptation mediated by cis-regulatory change. A fragment of an Accord transposable element inserted upstream of the Cyp6g1 gene is causally a...

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Autores principales: Schmidt, Joshua M., Good, Robert T., Appleton, Belinda, Sherrard, Jayne, Raymant, Greta C., Bogwitz, Michael R., Martin, Jon, Daborn, Phillip J., Goddard, Mike E., Batterham, Philip, Robin, Charles
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891717/
https://www.ncbi.nlm.nih.gov/pubmed/20585622
http://dx.doi.org/10.1371/journal.pgen.1000998
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author Schmidt, Joshua M.
Good, Robert T.
Appleton, Belinda
Sherrard, Jayne
Raymant, Greta C.
Bogwitz, Michael R.
Martin, Jon
Daborn, Phillip J.
Goddard, Mike E.
Batterham, Philip
Robin, Charles
author_facet Schmidt, Joshua M.
Good, Robert T.
Appleton, Belinda
Sherrard, Jayne
Raymant, Greta C.
Bogwitz, Michael R.
Martin, Jon
Daborn, Phillip J.
Goddard, Mike E.
Batterham, Philip
Robin, Charles
author_sort Schmidt, Joshua M.
collection PubMed
description The increased transcription of the Cyp6g1 gene of Drosophila melanogaster, and consequent resistance to insecticides such as DDT, is a widely cited example of adaptation mediated by cis-regulatory change. A fragment of an Accord transposable element inserted upstream of the Cyp6g1 gene is causally associated with resistance and has spread to high frequencies in populations around the world since the 1940s. Here we report the existence of a natural allelic series at this locus of D. melanogaster, involving copy number variation of Cyp6g1, and two additional transposable element insertions (a P and an HMS-Beagle). We provide evidence that this genetic variation underpins phenotypic variation, as the more derived the allele, the greater the level of DDT resistance. Tracking the spatial and temporal patterns of allele frequency changes indicates that the multiple steps of the allelic series are adaptive. Further, a DDT association study shows that the most resistant allele, Cyp6g1-[BP], is greatly enriched in the top 5% of the phenotypic distribution and accounts for ∼16% of the underlying phenotypic variation in resistance to DDT. In contrast, copy number variation for another candidate resistance gene, Cyp12d1, is not associated with resistance. Thus the Cyp6g1 locus is a major contributor to DDT resistance in field populations, and evolution at this locus features multiple adaptive steps occurring in rapid succession.
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spelling pubmed-28917172010-06-28 Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus Schmidt, Joshua M. Good, Robert T. Appleton, Belinda Sherrard, Jayne Raymant, Greta C. Bogwitz, Michael R. Martin, Jon Daborn, Phillip J. Goddard, Mike E. Batterham, Philip Robin, Charles PLoS Genet Research Article The increased transcription of the Cyp6g1 gene of Drosophila melanogaster, and consequent resistance to insecticides such as DDT, is a widely cited example of adaptation mediated by cis-regulatory change. A fragment of an Accord transposable element inserted upstream of the Cyp6g1 gene is causally associated with resistance and has spread to high frequencies in populations around the world since the 1940s. Here we report the existence of a natural allelic series at this locus of D. melanogaster, involving copy number variation of Cyp6g1, and two additional transposable element insertions (a P and an HMS-Beagle). We provide evidence that this genetic variation underpins phenotypic variation, as the more derived the allele, the greater the level of DDT resistance. Tracking the spatial and temporal patterns of allele frequency changes indicates that the multiple steps of the allelic series are adaptive. Further, a DDT association study shows that the most resistant allele, Cyp6g1-[BP], is greatly enriched in the top 5% of the phenotypic distribution and accounts for ∼16% of the underlying phenotypic variation in resistance to DDT. In contrast, copy number variation for another candidate resistance gene, Cyp12d1, is not associated with resistance. Thus the Cyp6g1 locus is a major contributor to DDT resistance in field populations, and evolution at this locus features multiple adaptive steps occurring in rapid succession. Public Library of Science 2010-06-24 /pmc/articles/PMC2891717/ /pubmed/20585622 http://dx.doi.org/10.1371/journal.pgen.1000998 Text en Schmidt et al. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Schmidt, Joshua M.
Good, Robert T.
Appleton, Belinda
Sherrard, Jayne
Raymant, Greta C.
Bogwitz, Michael R.
Martin, Jon
Daborn, Phillip J.
Goddard, Mike E.
Batterham, Philip
Robin, Charles
Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus
title Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus
title_full Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus
title_fullStr Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus
title_full_unstemmed Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus
title_short Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus
title_sort copy number variation and transposable elements feature in recent, ongoing adaptation at the cyp6g1 locus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2891717/
https://www.ncbi.nlm.nih.gov/pubmed/20585622
http://dx.doi.org/10.1371/journal.pgen.1000998
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