Centro Internacional de Agricultura Tropical (CIAT), Apartado Aéreo 6713, Cali, Colombia.
BMC Genomics. 2009 Dec 23;10:629. doi: 10.1186/1471-2164-10-629.
Expressed sequence tags (ESTs) are an important source of gene-based markers such as those based on insertion-deletions (Indels) or single-nucleotide polymorphisms (SNPs). Several gel based methods have been reported for the detection of sequence variants, however they have not been widely exploited in common bean, an important legume crop of the developing world. The objectives of this project were to develop and map EST based markers using analysis of single strand conformation polymorphisms (SSCPs), to create a transcript map for common bean and to compare synteny of the common bean map with sequenced chromosomes of other legumes.
A set of 418 EST based amplicons were evaluated for parental polymorphisms using the SSCP technique and 26% of these presented a clear conformational or size polymorphism between Andean and Mesoamerican genotypes. The amplicon based markers were then used for genetic mapping with segregation analysis performed in the DOR364 x G19833 recombinant inbred line (RIL) population. A total of 118 new marker loci were placed into an integrated molecular map for common bean consisting of 288 markers. Of these, 218 were used for synteny analysis and 186 presented homology with segments of the soybean genome with an e-value lower than 7 x 10-12. The synteny analysis with soybean showed a mosaic pattern of syntenic blocks with most segments of any one common bean linkage group associated with two soybean chromosomes. The analysis with Medicago truncatula and Lotus japonicus presented fewer syntenic regions consistent with the more distant phylogenetic relationship between the galegoid and phaseoloid legumes.
The SSCP technique is a useful and inexpensive alternative to other SNP or Indel detection techniques for saturating the common bean genetic map with functional markers that may be useful in marker assisted selection. In addition, the genetic markers based on ESTs allowed the construction of a transcript map and given their high conservation between species allowed synteny comparisons to be made to sequenced genomes. This synteny analysis may support positional cloning of target genes in common bean through the use of genomic information from these other legumes.
表达序列标签(ESTs)是基因标记的重要来源,例如基于插入缺失(Indels)或单核苷酸多态性(SNPs)的标记。已经报道了几种基于凝胶的方法来检测序列变异,但它们在发展中国家重要的豆科作物普通豆中并未得到广泛应用。本项目的目的是开发和映射基于 EST 的标记,使用单链构象多态性(SSCP)分析,为普通豆创建转录图谱,并比较普通豆图谱与其他豆科植物测序染色体的同线性。
使用 SSCP 技术评估了一组 418 个基于 EST 的扩增子的亲本多态性,其中 26%的扩增子在安第斯和中美洲基因型之间表现出明显的构象或大小多态性。然后,使用基于扩增子的标记进行遗传作图,在 DOR364 x G19833 重组自交系(RIL)群体中进行分离分析。总共将 118 个新标记位点放置在普通豆的综合分子图谱中,该图谱由 288 个标记组成。其中,218 个用于同线性分析,186 个与大豆基因组的片段具有同源性,e 值低于 7 x 10-12。与大豆的同线性分析显示出同线性块的镶嵌模式,任何一个普通豆连锁群的大多数片段都与两个大豆染色体相关。与 Medicago truncatula 和 Lotus japonicus 的分析显示出较少的同线性区域,这与 galegoid 和 phaseoloid 豆科植物之间更远的系统发育关系一致。
SSCP 技术是一种有用且廉价的替代 SNP 或 Indel 检测技术,可用于用可能在标记辅助选择中有用的功能标记饱和普通豆遗传图谱。此外,基于 EST 的遗传标记允许构建转录图谱,并且由于它们在物种之间的高度保守性,允许与测序基因组进行同线性比较。这种同线性分析可以通过使用这些其他豆科植物的基因组信息,支持普通豆中目标基因的定位克隆。