Allele-tagged TaqMan® PCR genotyping assays for high-throughput detection of soybean cyst nematode resistance.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mariola Usovsky, Kristin Bilyeu, Andrew Bent, Andrew M Scaboo
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引用次数: 0

Abstract

Background: Whole genome resequencing (WGRS) platforms provide exceptional fingerprinting of the entire genome but are expensive and less flexible to use as a routine genotyping tool for targeting causal polymorphisms within a germplasm collection or breeding program. Therefore, there has been a continuous effort to develop small-scale genotyping platforms that facilitate robust and quick assessments of the allelic status of causal variants for important traits within soybean breeding programs. The objective was to develop a comprehensive panel of soybean cyst nematode (SCN) resistance TaqMan® assays via selecting the causative genes and analyzing their associated alleles.

Methods: The Soybean Allele Catalog was utilized to investigate WGRS-derived variants which are predicted to cause a change in the amino acid sequence of a gene product. This panel of TaqMan® assays reflects current knowledge about known SCN resistance-causing genes and their associated alleles: GmSNAP18-a and -b, GmSNAP11, GmSHMT08, GmSNAP15, GmNSFRAN07, and GmSNAP02-ins and -del. Developed assays were tested using elite breeding lines and segregating populations. TaqMan assays were compared to other currently available KASP and CAPS assays.

Conclusion: All assays showed excellent allele determination efficiencies. This SCN genotyping assay panel can be utilized as a simplified, accurate and reliable genotyping platform further equipping the updated soybean breeding toolbox.

等位基因标记TaqMan®PCR基因分型高通量检测大豆囊线虫抗性
背景:全基因组重测序(WGRS)平台提供了独特的全基因组指纹图谱,但作为一种常规基因分型工具,在种质收集或育种计划中靶向因果多态性是昂贵和不灵活的。因此,人们一直在努力开发小规模的基因分型平台,以促进对大豆育种计划中重要性状的因果变异的等位基因状态进行稳健和快速的评估。目的是通过选择致病基因和分析其相关等位基因,建立一套全面的大豆囊肿线虫(SCN)抗性TaqMan®检测方法。方法:利用大豆等位基因目录研究wgrs衍生的变异,这些变异预测会导致基因产物氨基酸序列的变化。这组TaqMan®检测反映了目前已知的SCN耐药基因及其相关等位基因:GmSNAP18-a和-b、GmSNAP11、GmSHMT08、GmSNAP15、GmNSFRAN07和GmSNAP02-ins和-del。开发的分析方法用优良的育种系和分离群体进行了测试。将TaqMan测定法与其他现有的KASP和CAPS测定法进行比较。结论:所有检测方法均具有良好的等位基因检测效率。该SCN基因分型检测板可作为一个简化、准确和可靠的基因分型平台,进一步装备更新的大豆育种工具箱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Biology Reports
Molecular Biology Reports 生物-生化与分子生物学
CiteScore
5.00
自引率
0.00%
发文量
1048
审稿时长
5.6 months
期刊介绍: Molecular Biology Reports publishes original research papers and review articles that demonstrate novel molecular and cellular findings in both eukaryotes (animals, plants, algae, funghi) and prokaryotes (bacteria and archaea).The journal publishes results of both fundamental and translational research as well as new techniques that advance experimental progress in the field and presents original research papers, short communications and (mini-) reviews.
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