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Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits
In depth studies of quantitative trait loci (QTL) can provide insights to the genetic architectures of complex traits. A major effect QTL at the distal end of chicken chromosome 1 has been associated with growth traits in multiple populations. This locus was fine-mapped in a fifteen-generation chick...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455696/ https://www.ncbi.nlm.nih.gov/pubmed/32859973 http://dx.doi.org/10.1038/s42003-020-01199-3 |
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author | Wang, Yuzhe Cao, Xuemin Luo, Chenglong Sheng, Zheya Zhang, Chunyuan Bian, Cheng Feng, Chungang Li, Jinxiu Gao, Fei Zhao, Yiqiang Jiang, Ziqin Qu, Hao Shu, Dingming Carlborg, Örjan Hu, Xiaoxiang Li, Ning |
author_facet | Wang, Yuzhe Cao, Xuemin Luo, Chenglong Sheng, Zheya Zhang, Chunyuan Bian, Cheng Feng, Chungang Li, Jinxiu Gao, Fei Zhao, Yiqiang Jiang, Ziqin Qu, Hao Shu, Dingming Carlborg, Örjan Hu, Xiaoxiang Li, Ning |
author_sort | Wang, Yuzhe |
collection | PubMed |
description | In depth studies of quantitative trait loci (QTL) can provide insights to the genetic architectures of complex traits. A major effect QTL at the distal end of chicken chromosome 1 has been associated with growth traits in multiple populations. This locus was fine-mapped in a fifteen-generation chicken advanced intercross population including 1119 birds and explored in further detail using 222 sequenced genomes from 10 high/low body weight chicken stocks. We detected this QTL that, in total, contributed 14.4% of the genetic variance for growth. Further, nine mosaic precise intervals (Kb level) which contain ancestral regulatory variants were fine-mapped and we chose one of them to demonstrate the key regulatory role in the duodenum. This is the first study to break down the detail genetic architectures for the well-known QTL in chicken and provides a good example of the fine-mapping of various of quantitative traits in any species. |
format | Online Article Text |
id | pubmed-7455696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74556962020-09-03 Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits Wang, Yuzhe Cao, Xuemin Luo, Chenglong Sheng, Zheya Zhang, Chunyuan Bian, Cheng Feng, Chungang Li, Jinxiu Gao, Fei Zhao, Yiqiang Jiang, Ziqin Qu, Hao Shu, Dingming Carlborg, Örjan Hu, Xiaoxiang Li, Ning Commun Biol Article In depth studies of quantitative trait loci (QTL) can provide insights to the genetic architectures of complex traits. A major effect QTL at the distal end of chicken chromosome 1 has been associated with growth traits in multiple populations. This locus was fine-mapped in a fifteen-generation chicken advanced intercross population including 1119 birds and explored in further detail using 222 sequenced genomes from 10 high/low body weight chicken stocks. We detected this QTL that, in total, contributed 14.4% of the genetic variance for growth. Further, nine mosaic precise intervals (Kb level) which contain ancestral regulatory variants were fine-mapped and we chose one of them to demonstrate the key regulatory role in the duodenum. This is the first study to break down the detail genetic architectures for the well-known QTL in chicken and provides a good example of the fine-mapping of various of quantitative traits in any species. Nature Publishing Group UK 2020-08-28 /pmc/articles/PMC7455696/ /pubmed/32859973 http://dx.doi.org/10.1038/s42003-020-01199-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Yuzhe Cao, Xuemin Luo, Chenglong Sheng, Zheya Zhang, Chunyuan Bian, Cheng Feng, Chungang Li, Jinxiu Gao, Fei Zhao, Yiqiang Jiang, Ziqin Qu, Hao Shu, Dingming Carlborg, Örjan Hu, Xiaoxiang Li, Ning Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits |
title | Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits |
title_full | Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits |
title_fullStr | Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits |
title_full_unstemmed | Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits |
title_short | Multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a QTL affecting chicken growth traits |
title_sort | multiple ancestral haplotypes harboring regulatory mutations cumulatively contribute to a qtl affecting chicken growth traits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455696/ https://www.ncbi.nlm.nih.gov/pubmed/32859973 http://dx.doi.org/10.1038/s42003-020-01199-3 |
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