Flowering time regulator qFT13‐3 involved in soybean adaptation to high latitudes

Author:

Li Yan‐fei123ORCID,Zhang Liya1,Wang Jun4ORCID,Wang Xing5,Guo Shiyu12,Xu Ze‐jun5,Li Delin12ORCID,Liu Zhangxiong12,Li Ying‐hui126ORCID,Liu Bin126ORCID,Qiu Li‐juan126ORCID

Affiliation:

1. The National Key Facility for Crop Gene Resources and Genetic Improvement (NFCRI) Institute of Crop Sciences Chinese Academy of Agricultural Sciences Beijing China

2. Key Laboratory of Crop Gene Resource and Germplasm Enhancement (MOA)/Key Laboratory of Soybean Biology (Beijing) (MOA) Institute of Crop Sciences Chinese Academy of Agricultural Sciences Beijing China

3. Key Lab of Chinese Medicine Resources Conservation State Administration of Traditional Chinese Medicine of the People's Republic of China Institute of Medicinal Plant Development Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

4. MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co‐construction by Ministry and Province) Jingzhou China

5. Xuzhou Institute of Agricultural Sciences of Xu‐huai Region of Jiangsu Xuzhou China

6. State Key Laboratory of Crop Gene Resources and Breeding Institute of Crop Sciences, Chinese Academy of Agricultural Sciences Beijing China

Abstract

SummarySoybean is a short‐day plant that typically flowers earlier when exposed to short‐day conditions. However, the identification of genes associated with earlier flowering time but without a yield penalty is rare. In this study, we conducted genome‐wide association studies (GWAS) using two re‐sequencing datasets that included 113 wild soybeans (G. soja) and 1192 cultivated soybeans (G. max), respectively, and simultaneously identified a candidate flowering gene, qFT13‐3, which encodes a protein homologous to the pseudo‐response regulator (PRR) transcription factor. We identified four major haplotypes of qFT13‐3 in the natural population, with haplotype H4 (qFT13‐3H4) being lost during domestication, while qFT13‐3H1 underwent natural and artificial selection, increasing in proportion from 4.5% in G. soja to 43.8% in landrace and to 81.9% in improve cultivars. Notably, most cultivars harbouring qFT13‐3H1 were located in high‐latitude regions. Knockout of qFT13‐3 accelerated flowering and maturity time under long‐day conditions, indicating that qFT13‐3 functions as a flowering inhibitor. Our results also showed that qFT13‐3 directly downregulates the expression of GmELF3b‐2 which is a component of the circadian clock evening complex. Field trials revealed that the qft13‐3 mutants shorten the maturity period by 11 days without a concomitant penalty on yield. Collectively, qFT13‐3 can be utilized for the breeding of high‐yield cultivars with a short maturity time suitable for high latitudes.

Publisher

Wiley

Subject

Plant Science,Agronomy and Crop Science,Biotechnology

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