Li Wentao, Zeng Ruizhen, Zhang Zemin, Ding Xiaohua, Zhang Guiquan
Guangdong Provincial Key Lab of Plant Molecular Breeding, South China Agricultural University, Guangzhou 510642, China.
Theor Appl Genet. 2008 May;116(7):915-22. doi: 10.1007/s00122-008-0723-5. Epub 2008 Feb 15.
The partial pollen abortion of hybrids between the indica and japonica subspecies of Asian cultivated rice is one of the major barriers in utilizing intersubspecific heterosis in hybrid rice breeding. Although a single hybrid pollen sterility locus may have little impact on spikelet fertility, the cumulative effect of several loci usually leads to a serious decrease in spikelet fertility. Isolating of the genes conferring hybrid pollen sterility is necessary to understand this phenomenon and to overcome the resulting genetic barrier. In this study, a new locus for F1 pollen sterility, S-d, was identified on the short arm of chromosome 1 by analyzing the genetic effect of substituted segments of the near-isogenic line E11-5 derived from the japonica variety Taichung 65 (recurrent parent) and the indica variety Dee-geo-woo-gen (donor parent). The S-d locus was first mapped to a 0.8 cM interval between SSR markers PSM46 and PSM80 using a F2 population of 125 individuals. The flanking markers were then used to identify recombinants from a population of 2,160 plants derived from heterozygotes of the primary F2 population. Simultaneously, additional markers were developed from genomic sequence divergence in this region. Analysis of the recombinants in the region resulted in the successful mapping of the S-d locus to a 67-kb fragment, containing 17 predicted genes. Positional cloning of this gene will contribute to our understanding of the molecular basis for partial pollen sterility of intersubspecific F1 hybrids in rice.
亚洲栽培稻籼粳亚种间杂种的部分花粉败育是杂交水稻育种中利用亚种间杂种优势的主要障碍之一。尽管单个杂种花粉不育位点对小穗育性的影响可能较小,但几个位点的累积效应通常会导致小穗育性严重下降。分离赋予杂种花粉不育的基因对于理解这一现象并克服由此产生的遗传障碍是必要的。在本研究中,通过分析源自粳稻品种台中65(轮回亲本)和籼稻品种地谷(供体亲本)的近等基因系E11-5的替代片段的遗传效应,在第1染色体短臂上鉴定出一个新的F1花粉不育位点S-d。利用125个个体的F2群体,首先将S-d位点定位到SSR标记PSM46和PSM80之间0.8 cM的区间。然后使用侧翼标记从源自初级F2群体杂合子的2160株植物群体中鉴定重组体。同时,从该区域的基因组序列差异中开发了额外的标记。对该区域重组体的分析导致S-d位点成功定位到一个67 kb的片段,其中包含17个预测基因。该基因的图位克隆将有助于我们理解水稻亚种间F1杂种部分花粉不育的分子基础。