Somyong Suthasinee, Ishikawa Goro, Munkvold Jesse D, Tanaka James, Benscher David, Cho Yong-Gu, Sorrells Mark E
Department of Plant Breeding and Genetics, Cornell University, 240 Emerson Hall, Ithaca, NY, 14853, USA.
Theor Appl Genet. 2014 Aug;127(8):1843-55. doi: 10.1007/s00122-014-2345-4. Epub 2014 Jul 2.
Fine mapping by recombinant backcross populations revealed that a preharvest sprouting QTL on 2B contained two QTLs linked in coupling with different effects on the phenotype. Wheat preharvest sprouting (PHS) occurs when grain germinates on the plant before harvest, resulting in reduced grain quality. Previous mapping of quantitative trait locus (QTL) revealed a major PHS QTL, QPhs.cnl-2B.1, located on chromosome 2B significant in 16 environments that explained from 5 to 31 % of the phenotypic variation. The objective of this project was to fine map the QPhs.cnl-2B.1 interval. Fine mapping was carried out in recombinant backcross populations (BC1F4 and BC1F5) that were developed by backcrossing selected doubled haploids to a recurrent parent and self-pollinating the BC1F4 and BC1F5 generations. In each generation, three markers in the QPhs.cnl-2B.1 interval were used to screen for recombinants. Fine mapping revealed that the QPhs.cnl-2B.1 interval contained two PHS QTLs linked in coupling. The distal PHS QTL, located between Wmc453c and Barc55, contributed 8 % of the phenotypic variation and also co-located with a major seed dormancy QTL determined by germination index. The proximal PHS QTL, between Wmc474 and CNL415-rCDPK, contributed 16 % of the variation. Several candidate genes including Mg-chelatase H subunit family protein, GTP-binding protein and calmodulin/Ca(2+)-dependent protein kinase were linked to the PHS QTL. Although many recombinant lines were identified, the lack of polymorphism for markers in the QTL interval prevented the localization of the recombination breakpoints and identification of the gene underlying the phenotype.
通过重组回交群体进行的精细定位表明,2B染色体上的一个收获前发芽QTL包含两个以相引相连锁的QTL,对表型有不同影响。小麦收获前发芽(PHS)是指籽粒在收获前在植株上发芽,导致籽粒品质下降。先前对数量性状基因座(QTL)的定位揭示了一个主要的PHS QTL,即位于2B染色体上的QPhs.cnl - 2B.1,在16种环境中显著,解释了5%至31%的表型变异。本项目的目的是对QPhs.cnl - 2B.1区间进行精细定位。精细定位在重组回交群体(BC1F4和BC1F5)中进行,这些群体是通过将选定的双单倍体与轮回亲本回交,并对BC1F4和BC1F5代进行自花授粉而培育的。在每一代中,使用QPhs.cnl - 2B.1区间内的三个标记筛选重组体。精细定位表明,QPhs.cnl - 2B.1区间包含两个以相引相连锁的PHS QTL。位于Wmc453c和Barc55之间的远端PHS QTL贡献了8%的表型变异,并且还与由发芽指数确定的一个主要种子休眠QTL共定位。位于Wmc474和CNL415 - rCDPK之间的近端PHS QTL贡献了16%的变异。包括镁螯合酶H亚基家族蛋白、GTP结合蛋白和钙调蛋白/Ca(2+)依赖性蛋白激酶在内的几个候选基因与PHS QTL连锁。尽管鉴定出了许多重组系,但QTL区间内标记缺乏多态性,阻碍了重组断点的定位和表型相关基因的鉴定。