Wan X Y, Wan J M, Jiang L, Wang J K, Zhai H Q, Weng J F, Wang H L, Lei C L, Wang J L, Zhang X, Cheng Z J, Guo X P
National Key Laboratory for Crop Genetics and Germplasm Enhancement, Jiangsu Plant Gene Engineering Research Center, Nanjing Agricultural University, 210095, Nanjing, China.
Theor Appl Genet. 2006 May;112(7):1258-70. doi: 10.1007/s00122-006-0227-0. Epub 2006 Feb 14.
Grain length in rice plays an important role in determining rice appearance, milling, cooking and eating quality. In this study, the genetic basis of grain length was dissected into six main-effect quantitative trait loci (QTLs) and twelve pairs of epistatic QTLs. The stability of these QTLs was evaluated in four environments using an F7 recombinant inbred line (RIL) population derived from the cross between a Japonica variety, Asominori, and an Indica variety, IR24. Moreover, chromosome segment substitution lines (CSSLs) harboring each of the six main-effect QTLs were used to evaluate gene action of QTLs across eight environments. A major QTL denoted as qGL-3a, was found to express stably not only in the isogenic background of Asominori but also in the recombinant background of Asominori and IR24 under multiple environments. The IR24 allele at qGL-3a has a positive effect on grain length. Based on the test of advanced backcross progenies, qGL-3a was dissected as a single Mendelian factor, i.e., long rice grain was controlled by a recessive gene gl-3. High-resolution genetic and physical maps were further constructed for fine mapping gl-3 by using 11 simple sequence repeat (SSR) markers designed using sequence information from seven BAC/PAC clones and a BC4F2 population consisting of 2,068 individuals. Consequently, the gl-3 gene was narrowed down to a candidate genomic region of 87.5 kb long defined by SSR markers RMw357 and RMw353 on chromosome 3, which provides a basis for map-based cloning of this gene and for marker-aided QTL pyramiding in rice quality breeding.
水稻粒长在决定稻米外观、加工、蒸煮和食用品质方面起着重要作用。本研究将粒长的遗传基础解析为6个主效数量性状基因座(QTL)和12对上位性QTL。利用粳稻品种“秋光”和籼稻品种“IR24”杂交衍生的F7重组自交系(RIL)群体,在4种环境下评估了这些QTL的稳定性。此外,利用携带6个主效QTL的染色体片段代换系(CSSL),在8种环境下评估了QTL的基因作用。发现一个名为qGL-3a的主效QTL不仅在“秋光”的近等基因背景中稳定表达,而且在多种环境下的“秋光”和“IR24”重组背景中也稳定表达。qGL-3a上的“IR24”等位基因对粒长有正向作用。基于高代回交后代的检测,qGL-3a被解析为一个单孟德尔因子,即长粒水稻由隐性基因gl-3控制。利用7个BAC/PAC克隆的序列信息设计的11个简单序列重复(SSR)标记和一个由2068个个体组成的BC4F2群体,进一步构建了高分辨率遗传图谱和物理图谱,对gl-3进行精细定位。结果,gl-3基因被定位到第3染色体上由SSR标记RMw357和RMw353界定的87.5 kb长的候选基因组区域,这为该基因的图位克隆以及水稻品质育种中标记辅助QTL聚合提供了基础。