Quantitative trait analysis of flowering time in spring rapeseed (B. napus L.)
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  • 作者:Y. X. Luo (1)
    C. Y. Luo (2)
    D. Z. Du (2) (3)
    Z. Fu (2) (3)
    Y. M. Yao (2) (3)
    C. C. Xu (1)
    H. S. Zhang (1)
  • 关键词:B. napus ; Flowering time ; QTL analysis ; DH lines
  • 刊名:Euphytica
  • 出版年:2014
  • 出版时间:December 2014
  • 年:2014
  • 卷:200
  • 期:3
  • 页码:321-335
  • 全文大小:1,034 KB
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  • 作者单位:Y. X. Luo (1)
    C. Y. Luo (2)
    D. Z. Du (2) (3)
    Z. Fu (2) (3)
    Y. M. Yao (2) (3)
    C. C. Xu (1)
    H. S. Zhang (1)

    1. College of Eco-Environmental Engineering, Qinghai University, Xining, 810016, Qinghai, People’s Republic of China
    2. Qinghai Academy of Agricultural and Forestry Sciences, Qinghai University, Xining, 810016, Qinghai, People’s Republic of China
    3. National Key Laboratory Breeding Base for Innovation and Utilization of Plateau Crop, Xining, 810016, Qinghai, People’s Republic of China
  • ISSN:1573-5060
文摘
The inheritance of flowering time trait in spring-type rapeseed (Brassica napus L.) is poorly understood, and the investigations on mapping of quantitative trait loci (QTL) for the trait are only few. We identified QTL underlying variation for flowering time in a doubled haploid (DH) mapping population of nonvernalization-responsive canola (B. napus L.) cultivar 465 and line 86 containing introgressions from Houyou11, a Chinese early-flowering cultivar in Brassica rapa L. Significant genetic variation in flowering time and response to photoperiod were observed among the DH lines from 465/86. A molecular linkage map was generated comprising three types of markers loci. QTL analysis indicated that flowering time is a complex trait and is controlled by at least 4 major loci, localized on four different linkage groups A6, A7, C8 and C9. These loci each accounted for between 9.2 and 12.56?% of the total genotypic variation for first flowering. The published high-density maps for flowering time mapping used different marker systems, and the parents of our crosses have different genetic origins, with either spring-type B. napus or B. rapa. So we cannot determine whether the QTL on the same linkage groups were in the same region or not. There was evidence of additive?×?additive epistatic effects for flowering time in the DH population. Epistasis existed not only between main-effect QTLs, but also between QTLs with minor effects. Four pair of epistasis effects between minor QTLs explained about 20?% of the genetic variance observed in the DH population. The results indicated that minor QTLs for flowering time should not be ignored. Significant genotypes?×?environment interactions were also found for the quantitative traits, and with significant change in the ranking of the DH lines in different environments. The results implied that FQ3 was a non-environment-specific QTL and may control flowering time by autonomous pathway. FQ4 were winter-environment-specific QTL and may control flowering time by photoperiod-pathway. Identification of the chromosomal location and effect of the genes influencing flowering time may hasten the development of canola varieties having an optimal time for flowering in target environments such as for high altitude areas, via marker-assisted selection.

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