Department of Plant Breeding and Biometry, Cornell University, 252 Emerson Hall, 14853, Ithaca, NY, USA.
Theor Appl Genet. 1991 Apr;81(4):471-6. doi: 10.1007/BF00219436.
Both Pi-2(t) and Pi-4(t) genes of rice confer complete resistance to the blast fungal pathogen Pyricularia oryzae Cav. As economically important plant genes, they have been recently characterized phenotypically, yet nothing is known about their classical linkage associations and gene products. We report here the isolation of DNA markers closely linked to these blast resistance genes in rice. The DNA markers were identified by testing 142 mapped rice genomic clones as hybridization probes against Southern blots, consisting of DNA from pairs of nearly isogenic lines (NILs) with or without the target genes. Chromosomal segments introgressed from donor genomes were distinguished by restriction fragment length polymorphisms (RFLPs) between the NILs. Linkage associations of the clones with Pi-2(t) and Pi4(t) were verified using F3 segregating populations of known blast reaction. Cosegregation of the resistant genotype and donor-derived allele indicated the presence of linkage between the DNA marker and a blast resistance gene. RFLP analysis showed that Pi-2(t) is closely linked to a single-copy DNA clone RG64 on chromosome 6, with a distance of 2.8+1.4(SE) cMorgans. Another blast resistance gene, Pi-4(t), is 15.3+4.2(SE) cMorgans away from a DNA clone RG869 on chromosome 12. These chromosomal regions can now be examined with additional markers to define the precise locations of Pi-2(t) and Pi-4(t). Tightly linked DNA markers may facilitate early selection for blast resistance genes in breeding programs. These markers may also be useful to map new genes for resistance to blast isolates. They may ultimately lead to the cloning of those genes via chromosome walking. The gene tagging approach demonstrated in this paper may apply to other genes of interest for both monogenic and polygenic traits.
Pi-2(t) 和 Pi-4(t) 这两个水稻基因赋予水稻对稻瘟病真菌病原体稻瘟病菌的完全抗性。作为具有重要经济意义的植物基因,它们最近在表型上得到了特征描述,但对于它们的经典连锁关联和基因产物却一无所知。我们在此报告了在水稻中分离与这些抗稻瘟病基因紧密连锁的 DNA 标记的方法。这些 DNA 标记是通过将 142 个已映射的水稻基因组克隆作为杂交探针进行测试来鉴定的,这些探针针对的是具有或不具有目标基因的近等基因系(NIL)的 Southern 印迹。通过在 NIL 之间区分来自供体基因组的染色体片段的限制性片段长度多态性(RFLP)来区分导入的染色体片段。使用具有已知抗稻瘟病反应的 F3 分离群体验证了克隆与 Pi-2(t) 和 Pi4(t) 的连锁关系。抗性基因型和供体衍生等位基因的共分离表明 DNA 标记与抗稻瘟病基因之间存在连锁。RFLP 分析表明,Pi-2(t) 与 6 号染色体上的单拷贝 DNA 克隆 RG64 紧密连锁,距离为 2.8+1.4(SE) 摩根。另一个抗稻瘟病基因 Pi-4(t) 距离 12 号染色体上的 DNA 克隆 RG869 有 15.3+4.2(SE) 摩根。现在可以在这些染色体区域使用额外的标记来确定 Pi-2(t) 和 Pi-4(t) 的精确位置。紧密连锁的 DNA 标记可以促进在育种计划中对抗稻瘟病基因的早期选择。这些标记也可能用于对抗稻瘟病分离物的抗性新基因的作图。它们最终可能通过染色体步移导致这些基因的克隆。本文中展示的基因标记方法可应用于单基因和多基因性状的其他感兴趣基因。