Efficient and fine mapping of RMES1 conferring resistance to sorghum aphid Melanaphis sacchari

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• 作者：Faming Wang (1)
  Songmin Zhao (2)
  Yonghua Han (1)
  Yutao Shao (1) (3)
  Zhenying Dong (1)
  Yang Gao (1)
  Kunpu Zhang (1)
  Xin Liu (1)
  Dawei Li (2)
  Jinhua Chang (4)
  Daowen Wang (1)
  
• 关键词：Fine mapping ; RMES1 ; Molecular marker ; Melanaphis sacchari ; Aphid ; Sorghum
• 刊名：Molecular Breeding
• 出版年：2013
• 出版时间：April 2013
• 年：2013
• 卷：31
• 期：4
• 页码：777-784
• 全文大小：380KB
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• 作者单位：Faming Wang (1)
  Songmin Zhao (2)
  Yonghua Han (1)
  Yutao Shao (1) (3)
  Zhenying Dong (1)
  Yang Gao (1)
  Kunpu Zhang (1)
  Xin Liu (1)
  Dawei Li (2)
  Jinhua Chang (4)
  Daowen Wang (1)
  
  1. The State Key Laboratory of Plant Cell and Chromosome Engineering, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China
  2. The State Key Laboratory of Agro-Biotechnology, China Agricultural University, Beijing, 100193, China
  3. Graduate University of Chinese Academy of Sciences, Yuquan Road, Beijing, 100039, China
  4. College of Agronomy, Agricultural University of Hebei, Baoding, 071001, China
  
• ISSN：1572-9788

文摘

Melanaphis sacchari causes serious damage to sorghum (Sorghum bicolor (L.) Moench) growth, development and productivity in many countries. A dominant gene (RMES1) conferring resistance to M. sacchari has been found in the grain sorghum variety Henong 16 (HN16), but fine mapping of the RMES1 locus remains to be reported. In this study, genetic populations segregating for RMES1 were prepared with HN16 and BTx623 as parental lines. The latter had been used for sorghum genome sequencing but was found to be susceptible to M. sacchari in this work. A total of 11 molecular markers were mapped to the short arm of chromosome 6 harboring RMES1. The closest markers flanking the RMES1 locus were Sb6m2650 and Sb6rj2776, which delimited a chromosomal region of about 126?kb containing five predicted genes. The utility of the newly identified DNA markers for tagging RMES1 in molecular breeding of M. sacchari resistance, and further efforts in cloning RMES1, are discussed.