Identification of the causal mutation in early heading mutant of bread wheat (Triticum aestivum L.) using MutMap approach.

IF 2.6 3区 农林科学 Q1 AGRONOMY
Molecular Breeding Pub Date : 2024-05-21 eCollection Date: 2024-06-01 DOI:10.1007/s11032-024-01478-5
Shoya Komura, Kentaro Yoshida, Hironobu Jinno, Youko Oono, Hirokazu Handa, Shigeo Takumi, Fuminori Kobayashi
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Abstract

In bread wheat (Triticum aestivum L.), fine-tuning the heading time is essential to maximize grain yield. Photoperiod-1 (Ppd-1) and VERNALIZATION 1 (Vrn-1) are major genes affecting photoperiod sensitivity and vernalization requirements, respectively. These genes have predominantly governed heading timing. However, Ppd-1 and Vrn-1 significantly impact heading dates, necessitating another gene that can slightly modify heading dates for fine-tuning. In this study, we developed an early heading mutant from the ethyl methanesulfonate-mutagenized population of the Japanese winter wheat cultivar "Kitahonami." MutMap analysis identified a nonsense mutation in the clock component gene Wheat PHYTOCLOCK 1/LUX ARRHYTHMO (WPCL-D1) as the probable SNP responsible for the early heading mutant on chromosome 3D. Segregation analysis using F2 and F3 populations confirmed that plants carrying the wpcl-D1 allele headed significantly earlier than those with the functional WPCL-D1. The early heading mutant exhibited increased expression levels of Ppd-1 and circadian clock genes, such as WPCL1 and LATE ELONGATED HYPOCOTYL (LHY). Notably, the transcript accumulation levels of Ppd-A1 and Ppd-D1 were influenced by the copy number of the functional WPCL1 gene. These results suggest that a loss-of-function mutation in WPCL-D1 is the causal mutation for the early heading phenotype. Adjusting the functional copy number of WPCL1 will be beneficial in fine-tuning of heading dates.

Supplementary information: The online version contains supplementary material available at 10.1007/s11032-024-01478-5.

Abstract Image

利用 MutMap 方法鉴定面包小麦(Triticum aestivum L. )早穗突变体的致病突变。
在面包小麦(Triticum aestivum L.)中,要使谷物产量最大化,就必须对打顶时间进行微调。光周期-1(Ppd-1)和春化 1(Vrn-1)分别是影响光周期敏感性和春化要求的主要基因。这些基因主要控制着头状花序的时间。然而,Ppd-1 和 Vrn-1 对打顶时间有显著影响,因此需要另一种能轻微改变打顶时间的基因来进行微调。在这项研究中,我们从日本冬小麦栽培品种 "Kitahonami "的甲磺酸乙酯突变群体中培育出了一个早熟突变体。MutMap 分析确定了时钟组成基因 Wheat PHYTOCLOCK 1/LUX ARRHYTHMO (WPCL-D1) 中的一个无义突变,该突变可能是染色体 3D 上导致早熟突变体的 SNP。利用 F2 和 F3 群体进行的分离分析证实,携带 wpcl-D1 等位基因的植株比携带功能性 WPCL-D1 的植株早熟。早头突变体表现出 Ppd-1 和昼夜节律钟基因(如 WPCL1 和 LATE ELONGATED HYPOCOTYL (LHY))表达水平的升高。值得注意的是,Ppd-A1 和 Ppd-D1 的转录本积累水平受功能性 WPCL1 基因拷贝数的影响。这些结果表明,WPCL-D1的功能缺失突变是早茎表型的因果突变。调整 WPCL1 基因的功能拷贝数将有利于标题日期的微调:在线版本包含补充材料,见 10.1007/s11032-024-01478-5。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Breeding
Molecular Breeding 农林科学-农艺学
CiteScore
5.60
自引率
6.50%
发文量
67
审稿时长
1.5 months
期刊介绍: Molecular Breeding is an international journal publishing papers on applications of plant molecular biology, i.e., research most likely leading to practical applications. The practical applications might relate to the Developing as well as the industrialised World and have demonstrable benefits for the seed industry, farmers, processing industry, the environment and the consumer. All papers published should contribute to the understanding and progress of modern plant breeding, encompassing the scientific disciplines of molecular biology, biochemistry, genetics, physiology, pathology, plant breeding, and ecology among others. Molecular Breeding welcomes the following categories of papers: full papers, short communications, papers describing novel methods and review papers. All submission will be subject to peer review ensuring the highest possible scientific quality standards. Molecular Breeding core areas: Molecular Breeding will consider manuscripts describing contemporary methods of molecular genetics and genomic analysis, structural and functional genomics in crops, proteomics and metabolic profiling, abiotic stress and field evaluation of transgenic crops containing particular traits. Manuscripts on marker assisted breeding are also of major interest, in particular novel approaches and new results of marker assisted breeding, QTL cloning, integration of conventional and marker assisted breeding, and QTL studies in crop plants.
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