Mapping QTL for resistance to botrytis grey mould in chickpea
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  • 作者:Chetukuri Anuradha (12)
    Pooran M. Gaur (1) p.gaur@cgiar.org
    Suresh Pande (1)
    Kishore K. Gali (13)
    Muthyl Ganesh (2)
    Jagdish Kumar (14)
    Rajeev K. Varshney (15)
  • 关键词:Botrytis grey mould &#8211 ; Chickpea &#8211 ; Cicer arietinum L. &#8211 ; Linkage map &#8211 ; QTL mapping &#8211 ; Disease resistance
  • 刊名:Euphytica
  • 出版年:2011
  • 出版时间:November 2011
  • 年:2011
  • 卷:182
  • 期:1
  • 页码:1-9
  • 全文大小:1.7 MB
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  • 作者单位:1. International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru, Hyderabad, 502 324 AP, India2. Acharya NG Ranga Agricultural University, Rajendranagar, Hyderabad, 500 030 AP, India3. NRC Plant Biotechnology Institute (NRC-PBI), 110 Gymnasium Place, Saskatoon, SK S7N 0W9, Canada4. Hendrick Beans-for-Health Research Foundation, 11791 Sandy Row, Inkerman, ON K0E 1J0, Canada5. Generation Challenge Program (GCP), c/o CIMMYT, 06600 Mexico, DF, Mexico
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Plant Physiology
    Plant Sciences
    Ecology
  • 出版者:Springer Netherlands
  • ISSN:1573-5060
文摘
Botrytis grey mould (BGM) caused by Botrytis cinerea Pers. ex. Fr. is the second most important foliar disease of chickpea (Cicer arietinum L.) after ascochyta blight. An intraspecific linkage map of chickpea consisting of 144 markers assigned on 11 linkage groups was constructed from recombinant inbred lines (RILs) of a cross that involved a moderately resistant kabuli cultivar ICCV 2 and a highly susceptible desi cultivar JG 62. The length of the map obtained was 442.8 cM with an average interval length of 3.3 cM. Three quantitative trait loci (QTL) which together accounted for 43.6% of the variation for BGM resistance were identified and mapped on two linkage groups. QTL1 explained about 12.8% of the phenotypic variation for BGM resistance and was mapped on LG 6A. It was found tightly linked to markers SA14 and TS71rts36r at a LOD score of 3.7. QTL2 and QTL3 accounted for 9.5 and 48% of the phenotypic variation for BGM resistance, respectively, and were mapped on LG 3. QTL 2 was identified at LOD 2.7 and flanked by markers TA25 and TA144, positioned at 1 cM away from marker TA25. QTL3 was a strong QTL detected at LOD 17.7 and was flanked by TA159 at 12 cM distance on one side and TA118 at 4 cM distance on the other side. This is the first report on mapping of QTL for BGM resistance in chickpea. After proper validation, these QTL will be useful in marker-assisted pyramiding of BGM resistance in chickpea.

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