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Development of high amylose wheat through TILLING
BACKGROUND: Wheat (Triticum spp.) is an important source of food worldwide and the focus of considerable efforts to identify new combinations of genetic diversity for crop improvement. In particular, wheat starch composition is a major target for changes that could benefit human health. Starches wit...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424102/ https://www.ncbi.nlm.nih.gov/pubmed/22584013 http://dx.doi.org/10.1186/1471-2229-12-69 |
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author | Slade, Ann J McGuire, Cate Loeffler, Dayna Mullenberg, Jessica Skinner, Wayne Fazio, Gia Holm, Aaron Brandt, Kali M Steine, Michael N Goodstal, John F Knauf, Vic C |
author_facet | Slade, Ann J McGuire, Cate Loeffler, Dayna Mullenberg, Jessica Skinner, Wayne Fazio, Gia Holm, Aaron Brandt, Kali M Steine, Michael N Goodstal, John F Knauf, Vic C |
author_sort | Slade, Ann J |
collection | PubMed |
description | BACKGROUND: Wheat (Triticum spp.) is an important source of food worldwide and the focus of considerable efforts to identify new combinations of genetic diversity for crop improvement. In particular, wheat starch composition is a major target for changes that could benefit human health. Starches with increased levels of amylose are of interest because of the correlation between higher amylose content and elevated levels of resistant starch, which has been shown to have beneficial effects on health for combating obesity and diabetes. TILLING (Targeting Induced Local Lesions in Genomes) is a means to identify novel genetic variation without the need for direct selection of phenotypes. RESULTS: Using TILLING to identify novel genetic variation in each of the A and B genomes in tetraploid durum wheat and the A, B and D genomes in hexaploid bread wheat, we have identified mutations in the form of single nucleotide polymorphisms (SNPs) in starch branching enzyme IIa genes (SBEIIa). Combining these new alleles of SBEIIa through breeding resulted in the development of high amylose durum and bread wheat varieties containing 47-55% amylose and having elevated resistant starch levels compared to wild-type wheat. High amylose lines also had reduced expression of SBEIIa RNA, changes in starch granule morphology and altered starch granule protein profiles as evaluated by mass spectrometry. CONCLUSIONS: We report the use of TILLING to develop new traits in crops with complex genomes without the use of transgenic modifications. Combined mutations in SBEIIa in durum and bread wheat varieties resulted in lines with significantly increased amylose and resistant starch contents. |
format | Online Article Text |
id | pubmed-3424102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34241022012-08-22 Development of high amylose wheat through TILLING Slade, Ann J McGuire, Cate Loeffler, Dayna Mullenberg, Jessica Skinner, Wayne Fazio, Gia Holm, Aaron Brandt, Kali M Steine, Michael N Goodstal, John F Knauf, Vic C BMC Plant Biol Research Article BACKGROUND: Wheat (Triticum spp.) is an important source of food worldwide and the focus of considerable efforts to identify new combinations of genetic diversity for crop improvement. In particular, wheat starch composition is a major target for changes that could benefit human health. Starches with increased levels of amylose are of interest because of the correlation between higher amylose content and elevated levels of resistant starch, which has been shown to have beneficial effects on health for combating obesity and diabetes. TILLING (Targeting Induced Local Lesions in Genomes) is a means to identify novel genetic variation without the need for direct selection of phenotypes. RESULTS: Using TILLING to identify novel genetic variation in each of the A and B genomes in tetraploid durum wheat and the A, B and D genomes in hexaploid bread wheat, we have identified mutations in the form of single nucleotide polymorphisms (SNPs) in starch branching enzyme IIa genes (SBEIIa). Combining these new alleles of SBEIIa through breeding resulted in the development of high amylose durum and bread wheat varieties containing 47-55% amylose and having elevated resistant starch levels compared to wild-type wheat. High amylose lines also had reduced expression of SBEIIa RNA, changes in starch granule morphology and altered starch granule protein profiles as evaluated by mass spectrometry. CONCLUSIONS: We report the use of TILLING to develop new traits in crops with complex genomes without the use of transgenic modifications. Combined mutations in SBEIIa in durum and bread wheat varieties resulted in lines with significantly increased amylose and resistant starch contents. BioMed Central 2012-05-14 /pmc/articles/PMC3424102/ /pubmed/22584013 http://dx.doi.org/10.1186/1471-2229-12-69 Text en Copyright ©2012 Slade et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Slade, Ann J McGuire, Cate Loeffler, Dayna Mullenberg, Jessica Skinner, Wayne Fazio, Gia Holm, Aaron Brandt, Kali M Steine, Michael N Goodstal, John F Knauf, Vic C Development of high amylose wheat through TILLING |
title | Development of high amylose wheat through TILLING |
title_full | Development of high amylose wheat through TILLING |
title_fullStr | Development of high amylose wheat through TILLING |
title_full_unstemmed | Development of high amylose wheat through TILLING |
title_short | Development of high amylose wheat through TILLING |
title_sort | development of high amylose wheat through tilling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3424102/ https://www.ncbi.nlm.nih.gov/pubmed/22584013 http://dx.doi.org/10.1186/1471-2229-12-69 |
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