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Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01

BACKGROUND: A landmark in soybean research, Glyma1.01, the first whole genome sequence of variety Williams 82 (Glycine max L. Merr.) was completed in 2010 and is widely used. However, because the assembly was primarily built based on the linkage maps constructed with a limited number of markers and...

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Autores principales: Song, Qijian, Jenkins, Jerry, Jia, Gaofeng, Hyten, David L., Pantalone, Vince, Jackson, Scott A., Schmutz, Jeremy, Cregan, Perry B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704267/
https://www.ncbi.nlm.nih.gov/pubmed/26739042
http://dx.doi.org/10.1186/s12864-015-2344-0
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author Song, Qijian
Jenkins, Jerry
Jia, Gaofeng
Hyten, David L.
Pantalone, Vince
Jackson, Scott A.
Schmutz, Jeremy
Cregan, Perry B.
author_facet Song, Qijian
Jenkins, Jerry
Jia, Gaofeng
Hyten, David L.
Pantalone, Vince
Jackson, Scott A.
Schmutz, Jeremy
Cregan, Perry B.
author_sort Song, Qijian
collection PubMed
description BACKGROUND: A landmark in soybean research, Glyma1.01, the first whole genome sequence of variety Williams 82 (Glycine max L. Merr.) was completed in 2010 and is widely used. However, because the assembly was primarily built based on the linkage maps constructed with a limited number of markers and recombinant inbred lines (RILs), the assembled sequence, especially in some genomic regions with sparse numbers of anchoring markers, needs to be improved. Molecular markers are being used by researchers in the soybean community, however, with the updating of the Glyma1.01 build based on the high-resolution linkage maps resulting from this research, the genome positions of these markers need to be mapped. RESULTS: Two high density genetic linkage maps were constructed based on 21,478 single nucleotide polymorphism loci mapped in the Williams 82 x G. soja (Sieb. & Zucc.) PI479752 population with 1083 RILs and 11,922 loci mapped in the Essex x Williams 82 population with 922 RILs. There were 37 regions or single markers where marker order in the two populations was in agreement but was not consistent with the physical position in the Glyma1.01 build. In addition, 28 previously unanchored scaffolds were positioned. Map data were used to identify false joins in the Glyma1.01 assembly and the corresponding scaffolds were broken and reassembled to the new assembly, Wm82.a2.v1. Based upon the plots of the genetic on physical distance of the loci, the euchromatic and heterochromatic regions along each chromosome in the new assembly were delimited. Genomic positions of the commonly used markers contained in BARCSOYSSR_1.0 database and the SoySNP50K BeadChip were updated based upon the Wm82.a2.v1 assembly. CONCLUSIONS: The information will facilitate the study of recombination hot spots in the soybean genome, identification of genes or quantitative trait loci controlling yield, seed quality and resistance to biotic or abiotic stresses as well as other genetic or genomic research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2344-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-47042672016-01-08 Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01 Song, Qijian Jenkins, Jerry Jia, Gaofeng Hyten, David L. Pantalone, Vince Jackson, Scott A. Schmutz, Jeremy Cregan, Perry B. BMC Genomics Research Article BACKGROUND: A landmark in soybean research, Glyma1.01, the first whole genome sequence of variety Williams 82 (Glycine max L. Merr.) was completed in 2010 and is widely used. However, because the assembly was primarily built based on the linkage maps constructed with a limited number of markers and recombinant inbred lines (RILs), the assembled sequence, especially in some genomic regions with sparse numbers of anchoring markers, needs to be improved. Molecular markers are being used by researchers in the soybean community, however, with the updating of the Glyma1.01 build based on the high-resolution linkage maps resulting from this research, the genome positions of these markers need to be mapped. RESULTS: Two high density genetic linkage maps were constructed based on 21,478 single nucleotide polymorphism loci mapped in the Williams 82 x G. soja (Sieb. & Zucc.) PI479752 population with 1083 RILs and 11,922 loci mapped in the Essex x Williams 82 population with 922 RILs. There were 37 regions or single markers where marker order in the two populations was in agreement but was not consistent with the physical position in the Glyma1.01 build. In addition, 28 previously unanchored scaffolds were positioned. Map data were used to identify false joins in the Glyma1.01 assembly and the corresponding scaffolds were broken and reassembled to the new assembly, Wm82.a2.v1. Based upon the plots of the genetic on physical distance of the loci, the euchromatic and heterochromatic regions along each chromosome in the new assembly were delimited. Genomic positions of the commonly used markers contained in BARCSOYSSR_1.0 database and the SoySNP50K BeadChip were updated based upon the Wm82.a2.v1 assembly. CONCLUSIONS: The information will facilitate the study of recombination hot spots in the soybean genome, identification of genes or quantitative trait loci controlling yield, seed quality and resistance to biotic or abiotic stresses as well as other genetic or genomic research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-2344-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-06 /pmc/articles/PMC4704267/ /pubmed/26739042 http://dx.doi.org/10.1186/s12864-015-2344-0 Text en © Song et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Song, Qijian
Jenkins, Jerry
Jia, Gaofeng
Hyten, David L.
Pantalone, Vince
Jackson, Scott A.
Schmutz, Jeremy
Cregan, Perry B.
Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01
title Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01
title_full Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01
title_fullStr Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01
title_full_unstemmed Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01
title_short Construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly Glyma1.01
title_sort construction of high resolution genetic linkage maps to improve the soybean genome sequence assembly glyma1.01
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704267/
https://www.ncbi.nlm.nih.gov/pubmed/26739042
http://dx.doi.org/10.1186/s12864-015-2344-0
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