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

Author:

Komura Shoya1ORCID,Yoshida Kentaro1,Jinno Hironobu2,Oono Youko3,Handa Hirokazu4,Takumi Shigeo5,Kobayashi Fuminori3ORCID

Affiliation:

1. Kyoto University Graduate School of Agriculture Faculty of Agriculture: Kyoto Daigaku Nogaku Kenkyuka Nogakubu

2. Hokkaido Research Organization Kitami Agricultural Experiment Station

3. National Agriculture and Food Research Organization: Nogyo Shokuhin Sangyo Gijutsu Sogo Kenkyu Kiko

4. Kyoto Prefectural University School of Life and Environmental Sciences Graduate School of Life and Environmental Sciences: Kyoto Furitsu Daigaku Seimei Kankyo Gakubu Daigakuin Seimei Kankyogaku Kenkyuka

5. Kobe University Faculty of Agriculture Graduate School of Agricultural Science: Kobe Daigaku Daigakuin Nogaku Kenkyuka Nogakubu

Abstract

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.

Publisher

Research Square Platform LLC

Reference73 articles.

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