Gene Mapping of a Yellow-to-Lethal Mutation Based on Bulked-Segregant Analysis-Seq in Soybean

Author:

Wang Yaqi12ORCID,Chang Fangguo34,Al Amin G M5ORCID,Li Shuguang1,Fu Mengmeng1ORCID,Yu Xiwen1,Zhao Zhixin1,Xu Haifeng1,Zhao Tuanjie2ORCID

Affiliation:

1. Huai’an Key Laboratory for Agricultural Biotechnology, Key Laboratory of Germplasm Innovation in Lower Reaches of the Huaihe River, Ministry of Agriculture and Rural Affairs, Huaiyin Institute of Agricultural Sciences of Xuhuai Region in Jiangsu, Huai’an 223001, China

2. Soybean Research Institute, National Center for Soybean Improvement (Nanjing), Key Laboratory for Biology and Genetic Improvement of Soybean (General), Ministry of Agriculture and Rural Affairs, National Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing 210095, China

3. Agronomy College, Gansu Agricultural University, Lanzhou 730070, China

4. State Key Laboratory of Aridland Crop Science, Gansu Agricultural University, Lanzhou 730070, China

5. Department of Botany, Jagannath University, Dhaka 1100, Bangladesh

Abstract

Plant photosynthesis is mainly dependent on leaf color, and this has an impact on yield. Mutants lacking in chlorophyll have been analyzed to gain insight into the genetic processes involved in photosynthesis, chloroplast development, and chlorophyll metabolism. A yellow-to-lethal mutant, ytl, was selected from the M6 generation of the 60Coγ ray irradiation-treated soybean cultivar Nannong 1138-2. The mutant exhibited reduced chlorophyll content, with the thylakoid structure disrupted. Segregation of the cross between Williams 82 (W82) and ytl indicated that a recessive allele controlled yellow-to-lethal traits. The bulked-segregant analysis (BSA)-Seq method performed preliminary mapping, followed by simple sequence repeat (SSR) marker validation and further mapping. The candidate gene was mapped to a 418 Kb region containing 53 genes. High-throughput sequencing and first-generation sequencing results showed a two bp deletion in the second exon of Glyma.08g106500, leading to a frameshift mutation in ytl. As a promising candidate gene, Glyma.08g106500 encoded a chloroplast-localized pentatricopeptide repeat (PPR) domain-containing protein involved in the assembly of chloroplast proteins. These results will contribute to cloning the mutant ytl gene and provide insight into the regulatory processes controlling photosynthesis and chloroplast development and growth in soybean.

Funder

National Natural Science Foundation of China

Scientific Research Fund of Startup and Development for Introduced High-level Talents, Huai’an Academy of Agricultural Sciences, China

Research and Development Fund Project of Huai’an Academy of Agricultural Sciences, China

Core Technology Development for Breeding Program of Jiangsu Province

Jiangsu Collaborative Innovation Center for Modern Crop Production (JCIC-MCP) Program

Publisher

MDPI AG

Subject

Agronomy and Crop Science

Reference51 articles.

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