Cogan Noel O I, Ponting Rebecca C, Vecchies Anita C, Drayton Michelle C, George Julie, Dracatos Peter M, Dobrowolski Mark P, Sawbridge Timothy I, Smith Kevin F, Spangenberg Germán C, Forster John W
Primary Industries Research Victoria and Molecular Plant Breeding Cooperative Research Centre, Victorian AgriBiosciences Centre, La Trobe Research and Development Park, Bundoora, VIC, 3083, Australia.
Mol Genet Genomics. 2006 Aug;276(2):101-12. doi: 10.1007/s00438-006-0126-8. Epub 2006 May 17.
Molecular genetic marker development in perennial ryegrass has largely been dependent on anonymous sequence variation. The availability of a large-scale EST resource permits the development of functionally-associated genetic markers based on SNP variation in candidate genes. Genic SNP loci and associated haplotypes are suitable for implementation in molecular breeding of outbreeding forage species. Strategies for in vitro SNP discovery through amplicon cloning and sequencing have been designed and implemented. Putative SNPs were identified within and between the parents of the F(1)(NA(6) x AU(6)) genetic mapping family and were validated among progeny individuals. Proof-of-concept for the process was obtained using the drought tolerance-associated LpASRa2 gene. SNP haplotype structures were determined and correlated with predicted amino acid changes. Gene-length LD was evaluated across diverse germplasm collections. A survey of SNP variation across 100 candidate genes revealed a high frequency of SNP incidence (c. 1 per 54 bp), with similar proportions in exons and introns. A proportion (c. 50%) of the validated genic SNPs were assigned to the F(1)(NA(6) x AU(6)) genetic map, showing high levels of coincidence with previously mapped RFLP loci. The perennial ryegrass SNP resource will enable genetic map integration, detailed LD studies and selection of superior allele content during varietal development.
多年生黑麦草分子遗传标记的开发很大程度上依赖于匿名序列变异。大规模EST资源的可用性使得基于候选基因中SNP变异开发功能相关的遗传标记成为可能。基因SNP位点和相关单倍型适用于异交牧草物种的分子育种。通过扩增子克隆和测序进行体外SNP发现的策略已经设计并实施。在F(1)(NA(6)×AU(6))遗传作图群体的亲本内部和之间鉴定出推定的SNP,并在子代个体中进行了验证。使用与耐旱性相关的LpASRa2基因获得了该过程的概念验证。确定了SNP单倍型结构,并将其与预测的氨基酸变化相关联。在不同的种质资源库中评估了基因长度的连锁不平衡。对100个候选基因的SNP变异调查显示,SNP发生率很高(约每54 bp一个),外显子和内含子中的比例相似。约50%的已验证基因SNP被定位到F(1)(NA(6)×AU(6))遗传图谱上,与先前定位的RFLP位点高度一致。多年生黑麦草SNP资源将有助于遗传图谱整合、详细的连锁不平衡研究以及品种开发过程中优良等位基因含量的选择。