Xing Y Z, Tang W J, Xue W Y, Xu C G, Zhang Qifa
National Center of Plant Gene Research, Huazhong Agricultural University, Wuhan, 430070, China.
Theor Appl Genet. 2008 Apr;116(6):789-96. doi: 10.1007/s00122-008-0711-9. Epub 2008 Jan 25.
In our previous studies, one putative QTL affecting number of spikelets per panicle (SPP) was identified in the pericentromeric region of rice chromosome 7 using a recombinant inbred population. In order to define the QTL (qSPP7), RI50, a recombinant inbred line with 70% of genetic background same as the female parent of Zhenshan 97, was selected to produce near-isogenic lines for the target region in the present study. In a BC(2)F(2) population consisting of 190 plants, the frequency distribution of SPP was shown to be discontinuous and followed the expected Mendelian ratios (1:2:1 by progeny test) for single locus segregation. qSPP7 was mapped to a 0.4 cM region between SSR marker RM3859 and RFLP marker C39 based on tests of the BC(2)F(2) population and its progeny. Its additive and dominant effects on SPP were 51.1 and 24.9 spikelets, respectively. Of great interest, the QTL region also had effects on grain yield per plant (YD), 1,000 grain weight (GW), tillers per plant (TPP) and seed setting ratio (SR). Significant correlations were observed between SPP and YD (r = 0.66) and between SPP and SR (r = -0.29) in the progeny test. 1082 extremely small panicle plants of a BC(3)F(2) population containing 8,400 individuals were further used to fine map the QTL. It turns out that qSPP7 co-segregated with two markers, RM5436 and RM5499 spanning a physical distance of 912.4 kb. Overall results suggested that recombination suppression occurred in the region and positional cloning strategy is infeasible for qSPP7 isolation. The higher grain yield of Minghui 63 homozygote as compared to the heterozygote suggested that Minghui 63 homozygote at qSPP7 in hybrid rice could further improve its yield.
在我们之前的研究中,利用重组自交群体在水稻第7染色体着丝粒区域鉴定出一个影响每穗小穗数(SPP)的假定QTL。为了界定该QTL(qSPP7),本研究选择了遗传背景与珍汕97母本相同率达70%的重组自交系RI50,用于构建目标区域的近等基因系。在一个由190株植株组成的BC(2)F(2)群体中,SPP的频率分布呈间断性,且符合单基因座分离的预期孟德尔比率(通过后代测验为1:2:1)。基于对BC(2)F(2)群体及其后代的测验,qSPP7被定位到SSR标记RM3859和RFLP标记C39之间0.4 cM的区域。其对SPP的加性效应和显性效应分别为51.1个小穗和24.9个小穗。非常有趣的是,该QTL区域对单株产量(YD)、千粒重(GW)、单株分蘖数(TPP)和结实率(SR)也有影响。在后代测验中,观察到SPP与YD之间存在显著相关性(r = 0.66),以及SPP与SR之间存在显著相关性(r = -0.29)。一个包含8400个个体的BC(3)F(2)群体中的1082株极小穗植株被进一步用于对该QTL进行精细定位。结果表明,qSPP7与两个标记RM5436和RM5499共分离,这两个标记跨越的物理距离为912.4 kb。总体结果表明该区域发生了重组抑制,通过图位克隆策略分离qSPP7是不可行的。明恢63纯合子的产量高于杂合子,这表明杂交水稻中qSPP7位点的明恢63纯合子可进一步提高其产量。