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Using high-throughput sequencing to investigate the evolution of self-incompatibility genes in the Brassicaceae: strategies and challenges

机译:使用高通量测序研究十字花科自交不亲和基因的进化:策略和挑战

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Background: The high polymorphism of genes under long-term balancing selection makes efficient genotyping of large numbers of individuals difficult, particularly when they are members of a gene family. For the Major Histocompatibility Complex (MHC) in animals, 454 amplicon sequencing has been used to obtain sequences from duplicated loci in multiple individuals, as an alternative to traditional cloning and sequencing approaches. Aims: The purpose of this study was to assess the potential for using 454 sequencing to study other loci under balancing selection: genes involved in plant self-incompatibility (SI). As a test case, we focus on diploids and tetraploids in the genus Arabidopsis. Methods: We used four previously developed primer combinations that amplify a range of alleles of the pistil gene, SRK, and its previously recognised paralogs. The amplification products from duplicate polymerase chain reactions were separately pooled from each individual, tagged and sequenced. Reads were clustered and classified using a reference database of SRK and its known paralogs. Duplicate sets of reactions and individuals with known genotypes were used to assess error rates and the efficiency of clustering. Results: After preprocessing, the few remaining sequencing errors and chimeric sequences did not affect the resolution of genotypes. Optimal clustering was obtained with a 90% sequence similarity criterion and excluding sequences present at a frequency of less than 7% of the total reads for an individual. Conclusions: The protocol is promising for efficiently genotyping large numbers of individuals for highly variable gene families. View full textDownload full textKeywords Arabidopsis , clustering, data processing, polymorphic gene family, SRK alleles, 454 tagged amplicon sequencingRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/17550874.2012.748098
机译:背景:长期平衡选择下基因的高度多态性使得难以对大量个体进行有效的基因分型,特别是当它们是基因家族的成员时。对于动物的主要组织相容性复合体(MHC),已使用454扩增子测序从多个个体的重复基因座中获得序列,作为传统克隆和测序方法的替代方法。目的:本研究的目的是评估在平衡选择下使用454测序研究其他基因座的潜力:涉及植物自交不亲和性(SI)的基因。作为测试用例,我们重点研究拟南芥属的二倍体和四倍体。方法:我们使用了四种先前开发的引物组合,可扩增雌蕊基因SRK及其先前公认的旁系同源物的一系列等位基因。将来自重复聚合酶链反应的扩增产物分别与每个个体合并,标记并测序。使用SRK的参考数据库及其已知的同源物对读物进行聚类和分类。使用重复的反应集和具有已知基因型的个体来评估错误率和聚类效率。结果:预处理后,剩余的少量测序错误和嵌合序列不影响基因型的分辨率。使用90%的序列相似性标准获得了最佳的聚类结果,并且排除了以低于个体总读数的7%的频率存在的序列。结论:该协议有望有效地对高度可变的基因家族的大量个体进行基因分型。查看全文下载关键词拟南芥属,聚类,数据处理,多态基因家族,SRK等位基因,454个标记的扩增子测序相关var addthis_config = { ,facebook,stumbleupon,digg,google,更多”,发布号:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/17550874.2012.748098

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