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Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines
The Drosophila melanogaster Genetic Reference Panel (DGRP) is a community resource of 205 sequenced inbred lines, derived to improve our understanding of the effects of naturally occurring genetic variation on molecular and organismal phenotypes. We used an integrated genotyping strategy to identify...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079974/ https://www.ncbi.nlm.nih.gov/pubmed/24714809 http://dx.doi.org/10.1101/gr.171546.113 |
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author | Huang, Wen Massouras, Andreas Inoue, Yutaka Peiffer, Jason Ràmia, Miquel Tarone, Aaron M. Turlapati, Lavanya Zichner, Thomas Zhu, Dianhui Lyman, Richard F. Magwire, Michael M. Blankenburg, Kerstin Carbone, Mary Anna Chang, Kyle Ellis, Lisa L. Fernandez, Sonia Han, Yi Highnam, Gareth Hjelmen, Carl E. Jack, John R. Javaid, Mehwish Jayaseelan, Joy Kalra, Divya Lee, Sandy Lewis, Lora Munidasa, Mala Ongeri, Fiona Patel, Shohba Perales, Lora Perez, Agapito Pu, LingLing Rollmann, Stephanie M. Ruth, Robert Saada, Nehad Warner, Crystal Williams, Aneisa Wu, Yuan-Qing Yamamoto, Akihiko Zhang, Yiqing Zhu, Yiming Anholt, Robert R.H. Korbel, Jan O. Mittelman, David Muzny, Donna M. Gibbs, Richard A. Barbadilla, Antonio Johnston, J. Spencer Stone, Eric A. Richards, Stephen Deplancke, Bart Mackay, Trudy F.C. |
author_facet | Huang, Wen Massouras, Andreas Inoue, Yutaka Peiffer, Jason Ràmia, Miquel Tarone, Aaron M. Turlapati, Lavanya Zichner, Thomas Zhu, Dianhui Lyman, Richard F. Magwire, Michael M. Blankenburg, Kerstin Carbone, Mary Anna Chang, Kyle Ellis, Lisa L. Fernandez, Sonia Han, Yi Highnam, Gareth Hjelmen, Carl E. Jack, John R. Javaid, Mehwish Jayaseelan, Joy Kalra, Divya Lee, Sandy Lewis, Lora Munidasa, Mala Ongeri, Fiona Patel, Shohba Perales, Lora Perez, Agapito Pu, LingLing Rollmann, Stephanie M. Ruth, Robert Saada, Nehad Warner, Crystal Williams, Aneisa Wu, Yuan-Qing Yamamoto, Akihiko Zhang, Yiqing Zhu, Yiming Anholt, Robert R.H. Korbel, Jan O. Mittelman, David Muzny, Donna M. Gibbs, Richard A. Barbadilla, Antonio Johnston, J. Spencer Stone, Eric A. Richards, Stephen Deplancke, Bart Mackay, Trudy F.C. |
author_sort | Huang, Wen |
collection | PubMed |
description | The Drosophila melanogaster Genetic Reference Panel (DGRP) is a community resource of 205 sequenced inbred lines, derived to improve our understanding of the effects of naturally occurring genetic variation on molecular and organismal phenotypes. We used an integrated genotyping strategy to identify 4,853,802 single nucleotide polymorphisms (SNPs) and 1,296,080 non-SNP variants. Our molecular population genomic analyses show higher deletion than insertion mutation rates and stronger purifying selection on deletions. Weaker selection on insertions than deletions is consistent with our observed distribution of genome size determined by flow cytometry, which is skewed toward larger genomes. Insertion/deletion and single nucleotide polymorphisms are positively correlated with each other and with local recombination, suggesting that their nonrandom distributions are due to hitchhiking and background selection. Our cytogenetic analysis identified 16 polymorphic inversions in the DGRP. Common inverted and standard karyotypes are genetically divergent and account for most of the variation in relatedness among the DGRP lines. Intriguingly, variation in genome size and many quantitative traits are significantly associated with inversions. Approximately 50% of the DGRP lines are infected with Wolbachia, and four lines have germline insertions of Wolbachia sequences, but effects of Wolbachia infection on quantitative traits are rarely significant. The DGRP complements ongoing efforts to functionally annotate the Drosophila genome. Indeed, 15% of all D. melanogaster genes segregate for potentially damaged proteins in the DGRP, and genome-wide analyses of quantitative traits identify novel candidate genes. The DGRP lines, sequence data, genotypes, quality scores, phenotypes, and analysis and visualization tools are publicly available. |
format | Online Article Text |
id | pubmed-4079974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40799742014-07-17 Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines Huang, Wen Massouras, Andreas Inoue, Yutaka Peiffer, Jason Ràmia, Miquel Tarone, Aaron M. Turlapati, Lavanya Zichner, Thomas Zhu, Dianhui Lyman, Richard F. Magwire, Michael M. Blankenburg, Kerstin Carbone, Mary Anna Chang, Kyle Ellis, Lisa L. Fernandez, Sonia Han, Yi Highnam, Gareth Hjelmen, Carl E. Jack, John R. Javaid, Mehwish Jayaseelan, Joy Kalra, Divya Lee, Sandy Lewis, Lora Munidasa, Mala Ongeri, Fiona Patel, Shohba Perales, Lora Perez, Agapito Pu, LingLing Rollmann, Stephanie M. Ruth, Robert Saada, Nehad Warner, Crystal Williams, Aneisa Wu, Yuan-Qing Yamamoto, Akihiko Zhang, Yiqing Zhu, Yiming Anholt, Robert R.H. Korbel, Jan O. Mittelman, David Muzny, Donna M. Gibbs, Richard A. Barbadilla, Antonio Johnston, J. Spencer Stone, Eric A. Richards, Stephen Deplancke, Bart Mackay, Trudy F.C. Genome Res Resource The Drosophila melanogaster Genetic Reference Panel (DGRP) is a community resource of 205 sequenced inbred lines, derived to improve our understanding of the effects of naturally occurring genetic variation on molecular and organismal phenotypes. We used an integrated genotyping strategy to identify 4,853,802 single nucleotide polymorphisms (SNPs) and 1,296,080 non-SNP variants. Our molecular population genomic analyses show higher deletion than insertion mutation rates and stronger purifying selection on deletions. Weaker selection on insertions than deletions is consistent with our observed distribution of genome size determined by flow cytometry, which is skewed toward larger genomes. Insertion/deletion and single nucleotide polymorphisms are positively correlated with each other and with local recombination, suggesting that their nonrandom distributions are due to hitchhiking and background selection. Our cytogenetic analysis identified 16 polymorphic inversions in the DGRP. Common inverted and standard karyotypes are genetically divergent and account for most of the variation in relatedness among the DGRP lines. Intriguingly, variation in genome size and many quantitative traits are significantly associated with inversions. Approximately 50% of the DGRP lines are infected with Wolbachia, and four lines have germline insertions of Wolbachia sequences, but effects of Wolbachia infection on quantitative traits are rarely significant. The DGRP complements ongoing efforts to functionally annotate the Drosophila genome. Indeed, 15% of all D. melanogaster genes segregate for potentially damaged proteins in the DGRP, and genome-wide analyses of quantitative traits identify novel candidate genes. The DGRP lines, sequence data, genotypes, quality scores, phenotypes, and analysis and visualization tools are publicly available. Cold Spring Harbor Laboratory Press 2014-07 /pmc/articles/PMC4079974/ /pubmed/24714809 http://dx.doi.org/10.1101/gr.171546.113 Text en © 2014 Huang et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0. |
spellingShingle | Resource Huang, Wen Massouras, Andreas Inoue, Yutaka Peiffer, Jason Ràmia, Miquel Tarone, Aaron M. Turlapati, Lavanya Zichner, Thomas Zhu, Dianhui Lyman, Richard F. Magwire, Michael M. Blankenburg, Kerstin Carbone, Mary Anna Chang, Kyle Ellis, Lisa L. Fernandez, Sonia Han, Yi Highnam, Gareth Hjelmen, Carl E. Jack, John R. Javaid, Mehwish Jayaseelan, Joy Kalra, Divya Lee, Sandy Lewis, Lora Munidasa, Mala Ongeri, Fiona Patel, Shohba Perales, Lora Perez, Agapito Pu, LingLing Rollmann, Stephanie M. Ruth, Robert Saada, Nehad Warner, Crystal Williams, Aneisa Wu, Yuan-Qing Yamamoto, Akihiko Zhang, Yiqing Zhu, Yiming Anholt, Robert R.H. Korbel, Jan O. Mittelman, David Muzny, Donna M. Gibbs, Richard A. Barbadilla, Antonio Johnston, J. Spencer Stone, Eric A. Richards, Stephen Deplancke, Bart Mackay, Trudy F.C. Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines |
title | Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines |
title_full | Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines |
title_fullStr | Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines |
title_full_unstemmed | Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines |
title_short | Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines |
title_sort | natural variation in genome architecture among 205 drosophila melanogaster genetic reference panel lines |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079974/ https://www.ncbi.nlm.nih.gov/pubmed/24714809 http://dx.doi.org/10.1101/gr.171546.113 |
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