Allelic Mutation Analysis of Three Male Sterile ms3 Mutants in Soybean
Author:
Affiliation:

College of Life Sciences, Northwest University /Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education /Shaanxi Province Key Laboratory of Biotechnology and Biochemical Engineering, Xi’an 710069

Clc Number:

Fund Project:

Foundation projects: National Natural Science Foundation of China(32000598);Shaanxi Province Department of Education Natural Science Project(19JK0858);Natural Science Basic Research Program of Shaanxi(2023-JC-YB-178);Shaanxi Fundamental Science Research Project for Chemistry & Biology (22JHZ007)

  • Article
  • |
  • Figures
  • |
  • Metrics
  • |
  • Reference
  • |
  • Related
  • |
  • Cited by
  • |
  • Materials
  • |
  • Comments
    Abstract:

    Soybean male sterile lines play vital value for developing hybrid soybean varieties, while the traditional three-line hybridization system has problems due to a limited number of restorer lines. The environmental sensitive genic male sterile (EGMS) line can switch fertility under different conditions. In this research, the phenotypes and mutation sites of the three independent mutants ms3 (Washington), ms3 (Flanagan) and ms3 (Plainview) were further studied. Phenotypic identification of sterility, high-throughput sequencing, molecular marker design and mutation site verification, analysis of the effect of mutation on MS3 protein structure, ms3 (Plainview) anther semi-thin section experiments were carried out separately. These results showed that most of the pollens are aborted, only sporadic pollen grains with irregular shape were stained by I2-KI dye in the anthers of the three mutants. High-throughput sequencing results showed that ms3 (Washington) and ms3 (Flanagan) had a large fragment insertion in the PHD coding region of the third exon of the gene MS3, eventually compromising the PHD domain of MS3 protein, which was named ms3-1. In ms3 (Plainview), there is one base pair deletion in the first exon of MS3, resulting in frameshift mutation encoding only 40 amino acids. The loss-of-function allele was named ms3-2. Through semi-thin section analysis of ms3 (Plainview), its tapetum layer and pollen development were abnormal at the middle and late anther development stage. In summary, this study provided materials and basis for future application and genetic modification of ms3 and MS3 in soybean breeding.

    Reference
    Related
    Cited by
Get Citation
Share
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:December 31,2023
  • Revised:
  • Adopted:
  • Online: June 11,2024
  • Published:
You are the th visitor 京ICP备09069690号-23
® 2024 All Rights Reserved
Supported by:Beijing E-Tiller Technology Development Co., Ltd.