el-Kharbotly A, Leonards-Schippers C, Huigen D J, Jacobsen E, Pereira A, Stiekema W J, Salamini F, Gebhardt C
Department of Plant Breeding, Wageningen Agricultural University, The Netherlands.
Mol Gen Genet. 1994 Mar;242(6):749-54. doi: 10.1007/BF00283432.
Phytophthora infestans (Mont.) de Bary is the most important fungal pathogen of the potato (Solanum tuberosum). The introduction of major genes for resistance from the wild species S. demissum into potato cultivars is the earliest example of breeding for resistance using wild germplasm in this crop. Eleven resistance alleles (R genes) are known, differing in the recognition of corresponding avirulence alleles of the fungus. The number of R loci, their positions on the genetic map and the allelic relationships between different R variants are not known, except that the R1 locus has been mapped to potato chromosome V. The objective of this work was the further genetic analysis of different R alleles in potato. Tetraploid potato cultivars carrying R alleles were reduced to the diploid level by inducing haploid parthenogenetic development of 2n female gametes. Of the 157 isolated primary dihaploids, 7 set seeds and carried the resistance alleles R1, R3 and R10 either individually or in combinations. Independent segregation of the dominant R1 and R3 alleles was demonstrated in two F1 populations of crosses among a dihaploid clone carrying R1 plus R3 and susceptible pollinators. Distorted segregation in favour of susceptibility was found for the R3 allele in 15 of 18 F1 populations analysed, whereas the R1 allele segregated with a 1:1 ratio as expected in five F1 populations. The mode of inheritance of the R10 allele could not be deduced as only very few F1 hybrids bearing R10 were obtained. Linkage analysis in two F1 populations between R1, R3 and RFLP markers of known position on the potato RFLP maps confirmed the position of the R1 locus on chromosome V and localized the second locus, R3, to a distal position on chromosome XI.
致病疫霉(Phytophthora infestans (Mont.) de Bary)是马铃薯(Solanum tuberosum)最重要的真菌病原体。将野生种德米氏茄(S. demissum)的主要抗性基因导入马铃薯品种是该作物利用野生种质进行抗性育种的最早实例。已知有11个抗性等位基因(R基因),它们对真菌相应无毒力等位基因的识别有所不同。除了R1位点已被定位到马铃薯的第V染色体上之外,R位点的数量、它们在遗传图谱上的位置以及不同R变体之间的等位基因关系均未知。这项工作的目的是对马铃薯中不同的R等位基因进行进一步的遗传分析。通过诱导2n雌配子的单倍体孤雌生殖发育,将携带R等位基因的四倍体马铃薯品种降低到二倍体水平。在157个分离的初级双单倍体中,有7个结籽并单独或组合携带抗性等位基因R1、R3和R10。在一个携带R1加R3的双单倍体克隆与感病授粉者杂交的两个F1群体中,证明了显性R1和R3等位基因的独立分离。在分析的18个F1群体中的15个中,发现R3等位基因存在偏向感病性的分离畸变,而在5个F1群体中,R1等位基因按预期的1:1比例分离。由于仅获得了极少数携带R10的F1杂种,因此无法推断R10等位基因的遗传模式。在两个F1群体中,对R1、R3与马铃薯RFLP图谱上已知位置的RFLP标记进行连锁分析,证实了R1位点在第V染色体上的位置,并将第二个位点R3定位到第XI染色体的远端位置。