Department of Agronomy, Chiayi Agricultrual Experiment Station, Taiwan Agricultural Research Institute, Chiayi, Taiwan.
Hereditas. 2010 Oct;147(5):225-36. doi: 10.1111/j.1601-5223.2010.02120.x. Epub 2010 Oct 18.
To facilitate genetic research, we constructed two linkage maps by employing two F₂ populations derived from rice inter-subspecific crosses, japonica Tainung 67 (TNG67)/indica Taichung Sen 10 (TCS10) and japonica TNG67/indica Taichung Sen 17 (TCS17). We established linkage map lengths of 1481.6 cM and 1267.4 cM with average intervals of 13.8 cM and 14.4 cM by using 107 and 88 PCR markers for coverage of 88% of the rice genome in TNG67/TCS10 and TNG67/TCS17, respectively. The discrepancy in genetic maps in the two populations could be due to different cross combinations, crossing-over events, progeny numbers and/or markers. The most plausible explanation was segregation distortion; 18 markers (16.8%) distributed at nine regions of seven chromosomes and 10 markers (11.4%) at four regions of four chromosomes displayed severe segregation distortion (p < 0.01)in TNG67/TCS10 and TNG67/TCS17, respectively. All segregation-distorted markers in these two populations corresponded to reported reproductive barriers, either gametophytic or zygotic genes but not to hybrid breakdown genes. The observed recombination frequency, which was higher or lower than the intrinsic frequency, revealed the association of segregation distortion skewed to the same or different genotypes at the consecutive markers. The segregation distortion, possibly caused by reproductive barriers, affects the evaluation recombination frequencies and consequently the linkage analysis of QTLs and positional cloning.
为了促进遗传研究,我们利用来自籼稻亚种间杂交的两个 F₂群体,即粳稻台农 67(TNG67)/籼稻台中 10 号(TCS10)和粳稻 TNG67/籼稻台中 17 号(TCS17),构建了两个连锁图谱。我们利用 107 个和 88 个 PCR 标记,分别在 TNG67/TCS10 和 TNG67/TCS17 中覆盖了 88%和 87%的水稻基因组,建立了长度分别为 1481.6 cM 和 1267.4 cM 的连锁图谱,平均间隔分别为 13.8 cM 和 14.4 cM。两个群体遗传图谱的差异可能是由于不同的杂交组合、交叉事件、后代数量和/或标记造成的。最可能的解释是分离失真;在 TNG67/TCS10 和 TNG67/TCS17 中,分别有 18 个标记(16.8%)分布在七个染色体的九个区域和 10 个标记(11.4%)分布在四个染色体的四个区域存在严重的分离失真(p < 0.01)。这两个群体中所有分离失真的标记都对应于已报道的生殖障碍,无论是配子体还是合子基因,但不是杂种败育基因。观察到的重组频率高于或低于固有频率,表明连续标记的分离失真与相同或不同基因型相关。这种分离失真可能是由生殖障碍引起的,它会影响 QTL 和定位克隆的重组频率评估和连锁分析。