Department of Animal and Aquacultural Sciences, Norwegian University of Life Sciences, Box 1432 As, Norway.
Genet Sel Evol. 2010 Jun 3;42(1):16. doi: 10.1186/1297-9686-42-16.
Detecting a QTL is only the first step in genetic improvement programs. When a QTL with desirable characteristics is found, e.g. in a wild or unimproved population, it may be interesting to introgress the detected QTL into the commercial population. One approach to shorten the time needed for introgression is to combine both QTL identification and introgression, into a single step. This combines the strengths of fine mapping and backcrossing and paves the way for introgression of desirable but unknown QTL into recipient animal and plant lines.
The method consisting in combining QTL mapping and gene introgression has been extended from inbred to outbred populations in which QTL allele frequencies vary both in recipient and donor lines in different scenarios and for which polygenic effects are included in order to model background genes. The effectiveness of the combined QTL detection and introgression procedure was evaluated by simulation through four backcross generations.
The allele substitution effect is underestimated when the favourable QTL allele is not fixed in the donor line. This underestimation is proportional to the frequency differences of the favourable QTL allele between the lines. In most scenarios, the estimates of the QTL location are unbiased and accurate. The retained donor chromosome segment and linkage drag are similar to expected values from other published studies.
In general, our results show that it is possible to combine QTL detection and introgression even in outbred species. Separating QTL mapping and introgression processes is often thought to be longer and more costly. However, using a combined process saves at least one generation. With respect to the linkage drag and obligatory drag, the results of the combined detection and introgression scheme are very similar to those of traditional introgression schemes.
检测到一个 QTL 仅仅是遗传改良计划的第一步。当在野生或未经改良的群体中发现具有理想特性的 QTL 时,例如,将检测到的 QTL 导入商业群体中可能会很有趣。缩短导入所需时间的一种方法是将 QTL 鉴定和导入结合到一个步骤中。这结合了精细映射和回交的优势,为将理想但未知的 QTL 导入受体动植物品系铺平了道路。
将 QTL 作图和基因导入相结合的方法已从近交群体扩展到了在不同情景下受体和供体品系中 QTL 等位基因频率均发生变化的远交群体中,并且包括多基因效应以模拟背景基因。通过四个回交世代的模拟来评估联合 QTL 检测和导入程序的有效性。
当有利 QTL 等位基因在供体品系中未固定时,等位基因替代效应会被低估。这种低估与等位基因在系间的有利 QTL 频率差异成正比。在大多数情况下,QTL 位置的估计是无偏且准确的。保留的供体染色体片段和连锁拖曳与其他已发表研究的预期值相似。
总体而言,我们的结果表明,即使在远交物种中也可以将 QTL 检测和导入结合起来。将 QTL 作图和导入过程分开通常被认为时间更长且成本更高。然而,使用联合过程至少节省了一代。就连锁拖曳和强制拖曳而言,联合检测和导入方案的结果与传统导入方案的结果非常相似。