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A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis
The Chinese mitten crab Eriocheir sinensis is the most economically important cultivated crab species in China, and its genome has a high number of chromosomes (2n = 146). To obtain sufficient markers for construction of a dense genetic map for this species, we employed the recently developed specif...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206627/ https://www.ncbi.nlm.nih.gov/pubmed/28045132 http://dx.doi.org/10.1038/srep39826 |
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author | Qiu, Gao-Feng Xiong, Liang-Wei Han, Zhi-Ke Liu, Zhi-Qiang Feng, Jian-Bin Wu, Xu-Gan Yan, Yin-Long Shen, Hong Huang, Long Chen, Li |
author_facet | Qiu, Gao-Feng Xiong, Liang-Wei Han, Zhi-Ke Liu, Zhi-Qiang Feng, Jian-Bin Wu, Xu-Gan Yan, Yin-Long Shen, Hong Huang, Long Chen, Li |
author_sort | Qiu, Gao-Feng |
collection | PubMed |
description | The Chinese mitten crab Eriocheir sinensis is the most economically important cultivated crab species in China, and its genome has a high number of chromosomes (2n = 146). To obtain sufficient markers for construction of a dense genetic map for this species, we employed the recently developed specific-locus amplified fragment sequencing (SLAF-seq) method for large-scale SNPs screening and genotyping in a F1 full-sib family of 149 individuals. SLAF-seq generated 127,677 polymorphic SNP markers, of which 20,803 valid markers were assigned into five segregation types and were used together with previous SSR markers for linkage map construction. The final integrated genetic map included 17,680 SNP and 629 SSR markers on the 73 linkage groups (LG), and spanned 14,894.9 cM with an average marker interval of 0.81 cM. QTL mapping localized three significant growth-related QTL to a 1.2 cM region in LG53 as well as 146 sex-linked markers in LG48. Genome-wide QTL-association analysis further identified four growth-related QTL genes named LNX2, PAK2, FMRFamide and octopamine receptors. These genes are involved in a variety of different signaling pathways including cell proliferation and growth. The map and SNP markers described here will be a valuable resource for the E. sinensis genome project and selective breeding programs. |
format | Online Article Text |
id | pubmed-5206627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52066272017-01-04 A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis Qiu, Gao-Feng Xiong, Liang-Wei Han, Zhi-Ke Liu, Zhi-Qiang Feng, Jian-Bin Wu, Xu-Gan Yan, Yin-Long Shen, Hong Huang, Long Chen, Li Sci Rep Article The Chinese mitten crab Eriocheir sinensis is the most economically important cultivated crab species in China, and its genome has a high number of chromosomes (2n = 146). To obtain sufficient markers for construction of a dense genetic map for this species, we employed the recently developed specific-locus amplified fragment sequencing (SLAF-seq) method for large-scale SNPs screening and genotyping in a F1 full-sib family of 149 individuals. SLAF-seq generated 127,677 polymorphic SNP markers, of which 20,803 valid markers were assigned into five segregation types and were used together with previous SSR markers for linkage map construction. The final integrated genetic map included 17,680 SNP and 629 SSR markers on the 73 linkage groups (LG), and spanned 14,894.9 cM with an average marker interval of 0.81 cM. QTL mapping localized three significant growth-related QTL to a 1.2 cM region in LG53 as well as 146 sex-linked markers in LG48. Genome-wide QTL-association analysis further identified four growth-related QTL genes named LNX2, PAK2, FMRFamide and octopamine receptors. These genes are involved in a variety of different signaling pathways including cell proliferation and growth. The map and SNP markers described here will be a valuable resource for the E. sinensis genome project and selective breeding programs. Nature Publishing Group 2017-01-03 /pmc/articles/PMC5206627/ /pubmed/28045132 http://dx.doi.org/10.1038/srep39826 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Qiu, Gao-Feng Xiong, Liang-Wei Han, Zhi-Ke Liu, Zhi-Qiang Feng, Jian-Bin Wu, Xu-Gan Yan, Yin-Long Shen, Hong Huang, Long Chen, Li A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis |
title | A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis |
title_full | A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis |
title_fullStr | A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis |
title_full_unstemmed | A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis |
title_short | A second generation SNP and SSR integrated linkage map and QTL mapping for the Chinese mitten crab Eriocheir sinensis |
title_sort | second generation snp and ssr integrated linkage map and qtl mapping for the chinese mitten crab eriocheir sinensis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206627/ https://www.ncbi.nlm.nih.gov/pubmed/28045132 http://dx.doi.org/10.1038/srep39826 |
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