中国水稻科学 ›› 2023, Vol. 37 ›› Issue (3): 244-252.DOI: 10.16819/j.1001-7216.2023.220601

• 研究报告 • 上一篇    下一篇

籼稻材料570011抗褐飞虱基因的遗传分析及鉴定

程玲1,2, 黄福钢3, 邱一埔3, 王心怡3, 舒宛2, 邱永福3, 李发活3,*()   

  1. 1粮食作物种质创新与遗传改良湖北省重点实验室, 武汉 430064
    2长江大学 农学院, 湖北 荆州 434025
    3广西大学 农学院/亚热带农业生物资源保护与利用国家重点实验室, 南宁 530004
  • 收稿日期:2022-06-01 修回日期:2022-07-12 出版日期:2023-05-10 发布日期:2023-05-16
  • 通讯作者: *email: 316801153@qq.com
  • 基金资助:
    中央引导地方科技发展资金专项(桂科ZY21195040);粮食作物种质创新与遗传改良湖北省重点实验室开放课题(2021lzjj09);广西水稻遗传育种重点实验室开放课题(2022-36-Z01-KF04)

Genetic Analysis and Identification of Brown Planthopper Resistance Gene in indica Rice Accession 570011

CHENG Ling1,2, HUANG Fugang3, QIU Yipu3, WANG Xinyi3, SHU Wan2, QIU Yongfu3, LI Fahuo3,*()   

  1. 1Hubei Key Laboratory of Food Crop Germplasm and Genetic Improvement, Wuhan 430064, China
    2College of Agriculture, Yangtze University, Jingzhou 434025, China
    3College of Agriculture, Guangxi University/State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Nanning 530004, China
  • Received:2022-06-01 Revised:2022-07-12 Online:2023-05-10 Published:2023-05-16
  • Contact: *email: 316801153@qq.com

摘要:

【目的】发掘籼稻570011中抗褐飞虱主效基因,为培育抗虫水稻新品种提供基因资源。【方法】采用苗期集团法对抗性亲本570011和感虫亲本9311杂交后代F3群体进行表型鉴定,结合F2群体基因型,使用作图软件构建染色体的局部遗传连锁图,对目标区段抗性位点进行检测和遗传效应评估。采用实时荧光定量PCR (qRT-PCR)分析定位区间内最可能的候选基因,并对其基因组序列进行测序,比较对应CDS和氨基酸序列并进行系统进化树分析。【结果】籼稻570011在苗期对褐飞虱表现高抗,且对褐飞虱有明显的抗生性和趋避性。统计发现F3群体抗虫株系数(抗性值<7)∶感虫株系数(抗性值≥7)为89∶35,卡方检验表明符合一对显性基因的分离规律。基因定位发现在第4染色体标记4M18.675和4M24.64之间的39 cM区域内检测到一个褐飞虱抗性位点,可能是已克隆基因BPH6的等位基因。qRT-PCR分析表明570011中Os04g35210BPH6等位基因)在褐飞虱取食后表达量显著高于感虫材料9311。570011中Os04g35210基因与BPH6的CDS和氨基酸序列同源性分别达到99.08%和97.96%,系统进化树分析发现两者的亲缘关系最近,表明该抗性基因是BPH6的等位基因。【结论】籼稻材料570011是一份高抗褐飞虱种质,其抗性表型受一个主效基因控制。该基因的发掘丰富了BPH6的等位型和抗源来源,为抗虫水稻育种提供新抗源。

关键词: 水稻, 褐飞虱, BPH6, 等位基因, 生理抗性机制

Abstract:

【Objective】The aim is to identify brown planthopper (BPH) resistance gene in resistant indica rice accession 570011, and provide new materials for insect-resistant rice breeding.【Method】A seedling bulk test was conducted to evaluate the BPH resistance of F3 population, and a local genetic map was developed based on the genotype of the mapping population by JoinMap 3.0. The resistance locus was then detected and genetic effect was evaluated by MapQTL 5. The expression of one candidate resistance gene was analyzed with qRT-PCR, and the corresponding CDS and amino acid sequences of the candidate gene were compared.【Result】Accession 570011 showed high resistance to BPH at the seedling stage and significant antibiosis and antixenosis against BPH. The ratio of resistant lines (score < 7) to susceptible lines (score≥7) in F3 population was 89:35, which accorded with the separation law of one dominant gene. One BPH resistance locus was detected in the 39 cM region flanked by markers 4M18675 and 4M24.64 on chromosome 4, which could be allelic to the cloned BPH6. qRT-PCR analysis indicated that the expression of BPH6 allele in accession 570011 was significantly higher than that in susceptible line 9311. Accession 570011 respectively shared the similarity of 99.08% and 97.96% in CDS and amino acid sequence comparing with the cloned gene BPH6. Moreover, they closely clustered in the phylogenetic tree. All the results suggested that the BPH resistance gene derived from accession 570011 was allelic to BPH6.【Conclusion】Accession 570011 is highly resistant to BPH and carries one major resistance gene, which is an allele of BPH6. The identification of the resistance gene enriches the alleles of BPH6 and provides new materials for insect resistant rice breeding.

Key words: Oryza sativa, brown planthopper, BPH6, allele, physiological resistance mechanism