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An RNA Sequencing Transcriptome Analysis of Grasspea (Lathyrus sativus L.) and Development of SSR and KASP Markers

机译:豌豆(Lathyrus sativus L.)的RNA测序转录组分析和SSR和KASP标记的发展。

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摘要

Grasspea (Lathyrus sativus L., 2n = 14) has great agronomic potential because of its ability to survive under extreme conditions, such as drought and flood. However, this legume is less investigated because of its sparse genomic resources and very slow breeding process. In this study, 570 million quality-filtered and trimmed cDNA sequence reads with total length of over 82 billion bp were obtained using the Illumina NextSeqTM 500 platform. Approximately two million contigs and 142,053 transcripts were assembled from our RNA-Seq data, which resulted in 27,431 unigenes with an average length of 1,250 bp and maximum length of 48,515 bp. The unigenes were of high-quality. For example, the stay-green (SGR) gene of grasspea was aligned with the SGR gene of pea with high similarity. Among these unigenes, 3,204 EST-SSR primers were designed, 284 of which were randomly chosen for validation. Of these validated unigenes, 87 (30.6%) EST-SSR primers produced polymorphic amplicons among 43 grasspea accessions selected from different geographical locations. Meanwhile, 146,406 SNPs were screened and 50 SNP loci were randomly chosen for the kompetitive allele-specific PCR (KASP) validation. Over 80% (42) SNP loci were successfully transformed to KASP markers. Comparison of the dendrograms according to the SSR and KASP markers showed that the different marker systems are partially consistent with the dendrogram constructed in our study.
机译:豌豆(Lathyrus sativus L.,2n = 14)具有巨大的农艺潜力,因为它具有在极端条件下生存的能力,例如干旱和洪水。但是,由于其豆科植物稀少的基因组资源和非常缓慢的繁殖过程,因此对其的研究较少。在这项研究中,使用Illumina NextSeq TM 500平台获得了5.7亿条经过质量过滤和修剪的cDNA序列读取,总长度超过820亿bp。从我们的RNA-Seq数据中组装了大约200万个重叠群和142,053个转录物,产生了27,431个单基因,平均长度为1,250 bp,最大长度为48,515 bp。单基因是高质量的。例如,草豌豆的保持绿色(SGR)基因与豌豆的SGR基因具有高度相似性。在这些单基因中,设计了3204种EST-SSR引物,随机选择了284种进行验证。在这些经过验证的单基因中,有87种(30.6%)EST-SSR引物在选自不同地理位置的43种豌豆种质中产生了多态性扩增子。同时,筛选了146,406个SNP,随机选择了50个SNP位点进行竞争性等位基因特异性PCR(KASP)验证。超过80%(42)SNP位点已成功转化为KASP标记。根据SSR和KASP标记对树状图进行比较,结果表明,不同的标记系统与我们研究中构建的树状图部分一致。

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