García R, Asíns M J, Forner J, Carbonell E A
Instituto Valenciano de Investigaciones Agrarias (IVIA), Apartado Oficial, 46113 Moncada (Valencia), Spain, ES.
Theor Appl Genet. 1999 Aug;99(3-4):511-8. doi: 10.1007/s001220051264.
Propagation of citrus rootstocks depends upon the production of clonal plants from nucellar seedlings. This makes apomixis one of the host important traits in breeding programs for citrus rootstocks. The genetic control of apomixis was studied in a 50-tree progeny derived from the cross C. volkameriana×P. trifoliata using 69 molecular markers and bulked segregant analysis. The proportion of nucellar seedlings was estimated by isoenzymatic analysis of 25 seedlings per tree for 2 consecutive years. The type of embryony (polyembryonic versus monoembryonic seeds) was also determined for fruit-yielding trees. Separate genetic maps for each parental species were developed. The integration and comparison of these maps could be accomplished using common multiallelic segregant loci. Differences in gene synteny between the two species-specific genetic maps were shown. Important distortions in the segregation of markers at several genomic regions, some of them also involving differences in the C-methylation pattern, have been observed, especially for the pollen parent. Analysis of quantitative trait loci (QTLs) revealed the presence of six genomic positions (two in P. trifoliata and four in C. volkameriana) contributing individually up to 24% of the total variation for apomixis. Within the same species, QTLs with positive and negative allele effects were present, even in the same linkage group. One of the markers associated to apomixis (Apo2) is also associated to embryony type. Therefore, the genetic control of apomictic reproduction found in citrus (nucellar embryony) is quite complex compared to what has been reported for gametophytic apomixis. Molecular markers linked to QTLs governing apomixis will be useful to assist selection of future apomictic rootstocks for citrus varieties.
柑橘砧木的繁殖依赖于珠心苗克隆植株的产生。这使得无融合生殖成为柑橘砧木育种计划中最重要的性状之一。利用69个分子标记和混合分组分析法,在由伏令夏橙×枳杂交产生的50株后代中研究了无融合生殖的遗传控制。连续两年通过对每棵树的25株幼苗进行同工酶分析来估计珠心苗的比例。还确定了结果树的胚性类型(多胚种子与单胚种子)。分别构建了每个亲本物种的遗传图谱。这些图谱的整合和比较可以通过共同的多等位基因分离位点来完成。显示了两个物种特异性遗传图谱之间基因同线性的差异。在几个基因组区域观察到标记分离的重要畸变,其中一些还涉及C-甲基化模式的差异,特别是对于花粉亲本。数量性状位点(QTL)分析揭示了六个基因组位置(枳中有两个,伏令夏橙中有四个)的存在,这些位置对无融合生殖的总变异贡献率分别高达24%。在同一物种内,即使在同一连锁群中,也存在具有正等位基因效应和负等位基因效应的QTL。与无融合生殖相关的一个标记(Apo2)也与胚性类型相关。因此,与配子体无融合生殖的报道相比,柑橘中发现的无融合生殖繁殖的遗传控制相当复杂。与控制无融合生殖的QTL连锁的分子标记将有助于为柑橘品种选择未来的无融合生殖砧木。