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TaGW2-A1中的一个剪接受体位点突变通过使籽粒更宽更长,增加了四倍体和六倍体小麦的千粒重。

A splice acceptor site mutation in TaGW2-A1 increases thousand grain weight in tetraploid and hexaploid wheat through wider and longer grains.

作者信息

Simmonds James, Scott Peter, Brinton Jemima, Mestre Teresa C, Bush Max, Del Blanco Alicia, Dubcovsky Jorge, Uauy Cristobal

机构信息

John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.

CEBAS-CSIC, Espinardo, P.O. Box 164, 30100, Murcia, Spain.

出版信息

Theor Appl Genet. 2016 Jun;129(6):1099-112. doi: 10.1007/s00122-016-2686-2. Epub 2016 Feb 16.

DOI:10.1007/s00122-016-2686-2
PMID:26883045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4869752/
Abstract

Across 13 experiments the gw2 - A1 mutant allele shifts grain size distribution consistently across all grains significantly increasing grain weight (6.6 %), width (2.8 %) and length (2.1 %) in tetraploid and hexaploid wheat. There is an urgent need to identify, understand and incorporate alleles that benefit yield in polyploid wheat. The rice OsGW2 gene functions as a negative regulator of grain weight and width and is homologous to the wheat TaGW2 gene. Previously it was shown that transcript levels of the A-genome homoeologue, TaGW2-A1, are negatively associated with grain width in hexaploid wheat. In this study we screened the tetraploid Kronos TILLING population to identify mutants in TaGW2-A1. We identified a G to A transition in the splice acceptor site of exon 5 which leads to mis-splicing in TaGW2-A1. We backcrossed the mutant allele into tetraploid and hexaploid wheat and generated a series of backcross derived isogenic lines which were evaluated in glasshouse and field conditions. Across 13 experiments the GW2-A1 mutant allele significantly increased thousand grain weight (6.6 %), grain width (2.8 %) and grain length (2.1 %) in tetraploid and hexaploid wheat compared to the wild type allele. In hexaploid wheat, this led to an increase in spike yield since no differences were detected for spikelet or grain number between isogenic lines. The increase in grain width and length was consistent across grains of different sizes, suggesting that the effect of the mutation is stable across the ear and within spikelets. Differences in carpel size and weight between alleles were identified as early as 5 days before anthesis, suggesting that TaGW2-A1 acts on maternal tissue before anthesis to restrict seed size. A single nucleotide polymorphism marker was developed to aid the deployment of the mutant allele into breeding programmes.

摘要

在13个实验中,gw2 - A1突变等位基因使四倍体和六倍体小麦所有籽粒的粒度分布一致地发生变化,显著增加了粒重(6.6%)、粒宽(2.8%)和粒长(2.1%)。迫切需要鉴定、了解并整合有益于多倍体小麦产量的等位基因。水稻OsGW2基因作为粒重和粒宽的负调控因子,与小麦TaGW2基因同源。此前研究表明,六倍体小麦中A基因组同源基因TaGW2 - A1的转录水平与粒宽呈负相关。在本研究中,我们筛选了四倍体 Kronos TILLING群体以鉴定TaGW2 - A1中的突变体。我们在第5外显子的剪接受体位点鉴定到一个由G到A的转变,这导致TaGW2 - A1发生错误剪接。我们将突变等位基因回交至四倍体和六倍体小麦中,并产生了一系列回交衍生的近等基因系,这些近等基因系在温室和田间条件下进行了评估。在13个实验中,与野生型等位基因相比,GW2 - A1突变等位基因在四倍体和六倍体小麦中显著增加了千粒重(6.6%)、粒宽(2.8%)和粒长(2.1%)。在六倍体小麦中,由于近等基因系之间的小穗数或粒数未检测到差异,这导致了穗产量的增加。粒宽和粒长的增加在不同大小的籽粒中是一致的,这表明该突变的影响在整个麦穗和小穗内是稳定的。早在开花前5天就鉴定到了等位基因之间的心皮大小和重量差异,这表明TaGW2 - A1在开花前作用于母体组织以限制种子大小。开发了一个单核苷酸多态性标记,以帮助将突变等位基因应用于育种计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/08464e917dce/122_2016_2686_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/0b8271172e37/122_2016_2686_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/5817229fd52e/122_2016_2686_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/3f6b5dff30e6/122_2016_2686_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/b92ed24719ea/122_2016_2686_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/08464e917dce/122_2016_2686_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/0b8271172e37/122_2016_2686_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/5817229fd52e/122_2016_2686_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/3f6b5dff30e6/122_2016_2686_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/b92ed24719ea/122_2016_2686_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1768/4869752/08464e917dce/122_2016_2686_Fig5_HTML.jpg

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