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Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat

Using Wheat 90 K SNP assay, kernel-related traits of Chinese bread wheat were used to perform association mapping in 14 environments by GWAS. Results indicated that 996 and 953 of 4417 and 3172 significant SNPs for kernel length and thousand-kernel weight were located on the chromosome 7B. Haplotype...

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Autores principales: Yan, Xuefang, Zhao, Lei, Ren, Yan, Dong, Zhongdong, Cui, Dangqun, Chen, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389898/
https://www.ncbi.nlm.nih.gov/pubmed/30804359
http://dx.doi.org/10.1038/s41598-019-38570-2
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author Yan, Xuefang
Zhao, Lei
Ren, Yan
Dong, Zhongdong
Cui, Dangqun
Chen, Feng
author_facet Yan, Xuefang
Zhao, Lei
Ren, Yan
Dong, Zhongdong
Cui, Dangqun
Chen, Feng
author_sort Yan, Xuefang
collection PubMed
description Using Wheat 90 K SNP assay, kernel-related traits of Chinese bread wheat were used to perform association mapping in 14 environments by GWAS. Results indicated that 996 and 953 of 4417 and 3172 significant SNPs for kernel length and thousand-kernel weight were located on the chromosome 7B. Haplotype analysis of these SNPs on 7B generated the block containing the predicted TaGW8-B1 gene. TaGW8-B1 gene was further cloned by sequencing in bread wheat and a 276-bp InDel was found in the first intron. TaGW8-B1 without and with the 276-bp InDel were designated as TaGW8-B1a and TaGW8-B1b, respectively. Analysis of agronomic traits indicated that cultivars with TaGW8-B1a possessed significantly wider kernel width, significantly more kernel number per spike, longer kernel length, higher thousand-kernel weight and more spikelet number per spike than cultivars with TaGW8-B1b. Furthermore, cultivars with TaGW8-B1a possessed significantly higher yield than cultivars with TaGW8-B1b. Therefore, TaGW8-B1a was considered as a potentially superior allele. Meanwhile, TaGW8-B1a possessed a significantly higher expression level than TaGW8-B1b in mature seeds by qRT-PCR. It possibly suggested that the high expression of TaGW8-B1 was positively associated with kernel size in bread wheat. Distribution of TaGW8-B1 allele indicated that TaGW8-B1a has been positively selected in Chinese wheat.
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spelling pubmed-63898982019-02-28 Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat Yan, Xuefang Zhao, Lei Ren, Yan Dong, Zhongdong Cui, Dangqun Chen, Feng Sci Rep Article Using Wheat 90 K SNP assay, kernel-related traits of Chinese bread wheat were used to perform association mapping in 14 environments by GWAS. Results indicated that 996 and 953 of 4417 and 3172 significant SNPs for kernel length and thousand-kernel weight were located on the chromosome 7B. Haplotype analysis of these SNPs on 7B generated the block containing the predicted TaGW8-B1 gene. TaGW8-B1 gene was further cloned by sequencing in bread wheat and a 276-bp InDel was found in the first intron. TaGW8-B1 without and with the 276-bp InDel were designated as TaGW8-B1a and TaGW8-B1b, respectively. Analysis of agronomic traits indicated that cultivars with TaGW8-B1a possessed significantly wider kernel width, significantly more kernel number per spike, longer kernel length, higher thousand-kernel weight and more spikelet number per spike than cultivars with TaGW8-B1b. Furthermore, cultivars with TaGW8-B1a possessed significantly higher yield than cultivars with TaGW8-B1b. Therefore, TaGW8-B1a was considered as a potentially superior allele. Meanwhile, TaGW8-B1a possessed a significantly higher expression level than TaGW8-B1b in mature seeds by qRT-PCR. It possibly suggested that the high expression of TaGW8-B1 was positively associated with kernel size in bread wheat. Distribution of TaGW8-B1 allele indicated that TaGW8-B1a has been positively selected in Chinese wheat. Nature Publishing Group UK 2019-02-25 /pmc/articles/PMC6389898/ /pubmed/30804359 http://dx.doi.org/10.1038/s41598-019-38570-2 Text en © The Author(s) 2019 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
Yan, Xuefang
Zhao, Lei
Ren, Yan
Dong, Zhongdong
Cui, Dangqun
Chen, Feng
Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat
title Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat
title_full Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat
title_fullStr Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat
title_full_unstemmed Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat
title_short Genome-wide association study revealed that the TaGW8 gene was associated with kernel size in Chinese bread wheat
title_sort genome-wide association study revealed that the tagw8 gene was associated with kernel size in chinese bread wheat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389898/
https://www.ncbi.nlm.nih.gov/pubmed/30804359
http://dx.doi.org/10.1038/s41598-019-38570-2
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