中国水稻科学 ›› 2014, Vol. 28 ›› Issue (5): 465-472.DOI: 10.3969/j.issn.1001-7216.2014.05.003

• 研究报告 • 上一篇    下一篇

水稻类病变突变体g303的鉴定和基因定位

刘林1,# ,张迎信1,# ,李枝1,2 ,刘群恩1 ,余宁1 ,孙滨1 ,杨正福1 ,周全1 ,程式华1 ,曹立勇1,*   

  1. 1中国水稻研究所/国家水稻改良中心/浙江省超级稻研究重点实验室,杭州 310006; 2杭州师范大学 生命与环境科学学院, 杭州 310036;
  • 收稿日期:2014-01-16 修回日期:2014-02-17 出版日期:2014-09-10 发布日期:2014-09-10
  • 通讯作者: 曹立勇1,*
  • 基金资助:

    国家转基因重大专项(2011ZX08001002); 国家自然科学基金资助项目(31071398, 31101203)。

Characterization and Gene Mapping of a Lesion Mimic Mutant g303 in Rice

LIU  Lin 1, # , ZHANG Yingxin 1, # , LI  Zhi 1,2 , LIU Qunen 1 , YU Ning 1 , SUN Bin 1 , YANG Zhengfu 1 , ZHOU  Quan 1 ,   CHENG  Shihua 1 ,   CAO Liyong 1,*   

  1. 1Zhejiang Key Laboratory of Super Rice/ National Center for Rice Improvement/China National Rice Research Institute, Hangzhou 310006, China;  2 College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou 310036, China;
  • Received:2014-01-16 Revised:2014-02-17 Online:2014-09-10 Published:2014-09-10
  • Contact: CAO Liyong1,*

摘要: 通过γ射线辐射诱变籼稻9311和中恢8015分别获得了2个类病变突变体g303和g342。g303播种4~5周叶片开始出现黄褐色斑点。随着植株的生长发育,至成熟期病斑几乎布满整个植株。与野生型相比,突变体g303株高、结实率、千粒重显著下降,叶绿素含量、光合速率显著降低。遗传分析表明,g303类病变性状由一对隐性基因控制。利用g303/日本晴F2群体进行定位,将突变基因定位于第12染色体标记InD10和InD12之间,遗传距离分别为0.19 cM和0.76 cM。测序分析发现,该基因与SL基因等位,其中g303和g342分别在编码区第572位和第1206位发生单碱基缺失,导致翻译提前终止。实时RTPCR结果显示抗病相关基因在突变体g303中表达量显著上升,说明该基因突变很可能激活了防卫反应。

关键词: 水稻, 类病变突变体, 基因定位, 防卫反应

Abstract: The lesion mimic mutant g303 and g342 were isolated by treating the seeds of indica varieties  9311 and R8015 with γray radiation, respectively. The yellow spots initially appear on g303 leaves at 4leaf stage. With the growth and development of the plant, the lesions almost occupied the whole plant till the maturity stage. Compared with the wild type, the plant height, seed setting rate and 1000grain weight of g303 significantly dropped, the chlorophyll and photosynthetic rate obviously decreased. Genetic analysis showed that the mutant phenotype was controlled by a single recessive gene. Using F2 mapping population of g303/ Nipponbare, the g303 mutant gene was mapped between marker InD10 and InD12 on rice chromosome 12, with genetic distances of 0.19 cM and 0.76 cM, respectively. Sequence analysis revealed that the mutated gene was allelic to SL, g303 and g342 mutated gene had a single nucleotide deletion (T572 and G1206, respectively), leading to a premature termination codon. Realtime PCR analysis showed that the expression level of defenserelated genes upregulated significantly, these results demonstrated that the mutation may activate the defense response.

Key words: rice, lesion mimic mutant, gene mapping, defense response

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