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Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean

KEY MESSAGE: We identified and characterized a mutant of soybean stachyose synthase gene controlling reduced stachyose content which benefit the soybean seed composition breeding program in the future. ABSTRACT: It has been shown that in soybean, increased sucrose and reduced raffinose family oligos...

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Autores principales: Qiu, Dan, Vuong, Tri, Valliyodan, Babu, Shi, Haiying, Guo, Binhui, Shannon, J. Grover, Nguyen, Henry T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624830/
https://www.ncbi.nlm.nih.gov/pubmed/26179337
http://dx.doi.org/10.1007/s00122-015-2575-0
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author Qiu, Dan
Vuong, Tri
Valliyodan, Babu
Shi, Haiying
Guo, Binhui
Shannon, J. Grover
Nguyen, Henry T.
author_facet Qiu, Dan
Vuong, Tri
Valliyodan, Babu
Shi, Haiying
Guo, Binhui
Shannon, J. Grover
Nguyen, Henry T.
author_sort Qiu, Dan
collection PubMed
description KEY MESSAGE: We identified and characterized a mutant of soybean stachyose synthase gene controlling reduced stachyose content which benefit the soybean seed composition breeding program in the future. ABSTRACT: It has been shown that in soybean, increased sucrose and reduced raffinose family oligosaccharides would have a positive impact on the world’s feed industry by improving digestibility and feed efficiency. We searched for new sources of modified oligosaccharide content in a subset of the USDA Soybean Germplasm Collection and then identified plant introduction (PI) 603176A as having ultra-low stachyose content (0.5 %). We identified a 33-bp deletion mutant in the putative stachyose synthase gene (STS gene, Glyma19g40550) of PI 603176A. A co-dominate indel marker was successfully developed from this 33-bp deletion area and was genetically mapped into two F(2:3) populations and a F(4:5) population, which associated with low stachyose content in the progeny lines. These observations provided strong evidence that the STS gene is responsible for stachyose biosynthesis in the soybean plant. Expression of the sts gene remained at the normal level, suggesting the loss of function in the gene is due to defective protein function. This gene-based perfect genetic marker for low stachyose content can be useful for marker-assisted selection in soybean molecular breeding programs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-015-2575-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-46248302015-11-03 Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean Qiu, Dan Vuong, Tri Valliyodan, Babu Shi, Haiying Guo, Binhui Shannon, J. Grover Nguyen, Henry T. Theor Appl Genet Original Article KEY MESSAGE: We identified and characterized a mutant of soybean stachyose synthase gene controlling reduced stachyose content which benefit the soybean seed composition breeding program in the future. ABSTRACT: It has been shown that in soybean, increased sucrose and reduced raffinose family oligosaccharides would have a positive impact on the world’s feed industry by improving digestibility and feed efficiency. We searched for new sources of modified oligosaccharide content in a subset of the USDA Soybean Germplasm Collection and then identified plant introduction (PI) 603176A as having ultra-low stachyose content (0.5 %). We identified a 33-bp deletion mutant in the putative stachyose synthase gene (STS gene, Glyma19g40550) of PI 603176A. A co-dominate indel marker was successfully developed from this 33-bp deletion area and was genetically mapped into two F(2:3) populations and a F(4:5) population, which associated with low stachyose content in the progeny lines. These observations provided strong evidence that the STS gene is responsible for stachyose biosynthesis in the soybean plant. Expression of the sts gene remained at the normal level, suggesting the loss of function in the gene is due to defective protein function. This gene-based perfect genetic marker for low stachyose content can be useful for marker-assisted selection in soybean molecular breeding programs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-015-2575-0) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2015-07-16 2015 /pmc/articles/PMC4624830/ /pubmed/26179337 http://dx.doi.org/10.1007/s00122-015-2575-0 Text en © The Author(s) 2015 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.
spellingShingle Original Article
Qiu, Dan
Vuong, Tri
Valliyodan, Babu
Shi, Haiying
Guo, Binhui
Shannon, J. Grover
Nguyen, Henry T.
Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean
title Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean
title_full Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean
title_fullStr Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean
title_full_unstemmed Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean
title_short Identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean
title_sort identification and characterization of a stachyose synthase gene controlling reduced stachyose content in soybean
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624830/
https://www.ncbi.nlm.nih.gov/pubmed/26179337
http://dx.doi.org/10.1007/s00122-015-2575-0
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