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甘蔗 ESTs 中单核甘酸多态性的特征分析

Characterisation of single nucleotide polymorphisms in sugarcane ESTs.

作者信息

Cordeiro Giovanni M, Eliott Frances, McIntyre C Lynne, Casu Rosanne E, Henry Robert J

机构信息

Centre for Plant Conservation Genetics, Southern Cross University, PO Box 157, Lismore 2480, Australia.

出版信息

Theor Appl Genet. 2006 Jul;113(2):331-43. doi: 10.1007/s00122-006-0300-8. Epub 2006 May 20.

Abstract

Commercial sugarcane cultivars (Saccharum spp. hybrids) are both polyploid and aneuploid with chromosome numbers in excess of 100; these chromosomes can be assigned to 8 homology groups. To determine the utility of single nucleotide polymorphisms (SNPs) as a means of improving our understanding of the complex sugarcane genome, we developed markers to a suite of SNPs identified in a list of sugarcane ESTs. Analysis of 69 EST contigs showed a median of 9 SNPs per EST and an average of 1 SNP per 50 bp of coding sequence. The quantitative presence of each base at 58 SNP loci within 19 contiguous sequence sets was accurately and reliably determined for 9 sugarcane genotypes, including both commercial cultivars and ancestral species, through the use of quantitative light emission technology in pyrophosphate sequencing. Across the 9 genotypes tested, 47 SNP loci were polymorphic and 11 monomorphic. Base frequency at individual SNP loci was found to vary approximately twofold between Australian sugarcane cultivars and more widely between cultivars and wild species. Base quantity was shown to segregate as expected in the IJ76-514 x Q165 sugarcane mapping population, indicating that SNPs that occur on one or two sugarcane chromosomes have the potential to be mapped. The use of SNP base frequencies from five of the developed markers was able to clearly distinguish all genotypes in the population. The use of SNP base frequencies from a further six markers within an EST contig was able to help establish the likely copy number of the locus in two genotypes tested. This is the first instance of a technology that has been able to provide an insight into the copy number of a specific gene locus in hybrid sugarcane. The identification of specific and numerous haplotypes/alleles present in a genotype by pyrophosphate sequencing or alternative techniques ultimately will provide the basis for identifying associations between specific alleles and phenotype and between allele dosage and phenotype in sugarcane.

摘要

商业甘蔗品种(甘蔗属杂交种)是多倍体和非整倍体,染色体数超过100条;这些染色体可分为8个同源组。为了确定单核苷酸多态性(SNP)作为增进我们对复杂甘蔗基因组理解的一种手段的效用,我们针对在一系列甘蔗EST中鉴定出的一组SNP开发了标记。对69个EST重叠群的分析表明,每个EST的SNP中位数为9个,编码序列每50 bp平均有1个SNP。通过在焦磷酸测序中使用定量发光技术,准确可靠地测定了9种甘蔗基因型(包括商业品种和原始物种)中19个连续序列集内58个SNP位点上每个碱基的定量存在情况。在测试的9种基因型中,47个SNP位点是多态性的,11个是单态性的。发现澳大利亚甘蔗品种之间单个SNP位点的碱基频率大约相差两倍,品种与野生种之间的差异更大。在IJ76 - 514×Q165甘蔗作图群体中,碱基数量如预期那样分离,这表明出现在一条或两条甘蔗染色体上的SNP有被作图的潜力。使用所开发的5个标记的SNP碱基频率能够清楚地区分群体中的所有基因型。在一个EST重叠群内使用另外6个标记的SNP碱基频率能够帮助确定所测试的两种基因型中该位点的可能拷贝数。这是一项技术首次能够深入了解杂交甘蔗中特定基因位点的拷贝数。通过焦磷酸测序或其他技术鉴定基因型中存在的特定且众多的单倍型/等位基因,最终将为确定甘蔗中特定等位基因与表型之间以及等位基因剂量与表型之间的关联提供基础。

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