National Key Laboratory of Crop Genetic Improvement, National Center of Rapeseed Improvement in Wuhan, Huazhong Agricultural University, Wuhan, Hubei, People's Republic of China.
Theor Appl Genet. 2012 Aug;125(4):695-705. doi: 10.1007/s00122-012-1861-3. Epub 2012 Apr 10.
One putative quantitative trait locus (QTL) for seeds per silique (SS), cqSS.A8, was identified using a double haploid (DH) population in Brassica napus, and near-isogenic lines (NILs; BC(3)F(1)) for cqSS.A8 were developed. However, the flanking markers from cqSS.A8 showed no significant difference using single-marker analysis, even though the frequency distribution of SS in the BC(3)F(1) was bimodal, suggesting that one novel locus existed. In this study, we characterized the effects of this locus in the NILs and used a published linkage map to determine its location. A three-step approach was designed for mapping the locus in the NILs (BC(3)F(2)): (1) determining the individual BC(3)F(2) genotype at the locus using a progeny test; (2) identifying amplified fragment length polymorphism (AFLP) markers linked to the locus using a combination of AFLP and bulked segregant analysis; and (3) determining the location and effects of this locus. QTL analysis in the BC(3)F(2) revealed that this locus explained 85.8 and 55.7 % of phenotypic variance for SS and SL, respectively. Its additive and dominant effects on SS were 6.1 and 5.7, respectively. The locus was validated using a DH population by composite interval mapping and located to linkage group C9 (designated as qSS.C9). Mapping qSS.C9 was undertaken using 230 extremely low-SS plants of a BC(4)F(1) population containing 807 plants. We found that qSS.C9 delimited a 1.005-Mb interval including 218 predicted genes in the reference Brassica rapa (Chiifu-401). These results will greatly facilitate map-based cloning of qSS.C9 and seed yield improvement in rapeseed.
一个假定的芸薹属作物每角粒数(SS)的数量性状位点(QTL),cqSS.A8,是使用油菜的双单倍体(DH)群体鉴定的,并开发了 cqSS.A8 的近等基因系(NIL;BC(3)F(1))。然而,即使在 BC(3)F(1)中 SS 的频率分布呈双峰,cqSS.A8 的侧翼标记在单标记分析中也没有显著差异,这表明存在一个新的基因座。在这项研究中,我们描述了该基因座在 NIL 中的效应,并使用已发表的连锁图谱来确定其位置。我们为 NIL(BC(3)F(2))中的基因座设计了一个三步映射方法:(1)使用后代测试确定个体 BC(3)F(2)基因型;(2)使用 AFLP 和混池分离分析相结合确定与该基因座连锁的扩增片段长度多态性(AFLP)标记;(3)确定该基因座的位置和效应。在 BC(3)F(2)中的 QTL 分析表明,该基因座分别解释了 SS 和 SL 表型方差的 85.8%和 55.7%。其对 SS 的加性和显性效应分别为 6.1 和 5.7。该基因座通过复合区间作图在 DH 群体中得到验证,并定位到连锁群 C9(命名为 qSS.C9)。使用包含 807 株植物的 BC(4)F(1)群体的 230 株极低 SS 植物进行 qSS.C9 的作图。我们发现 qSS.C9 限定了一个包含参考芸薹属植物(Chiifu-401)中 218 个预测基因的 1.005-Mb 区间。这些结果将极大地促进 qSS.C9 的图谱克隆和油菜种子产量的提高。