首页> 美国卫生研究院文献>other >Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding
【2h】

Gene Classification and Mining of Molecular Markers Useful in Red Clover (Trifolium pratense) Breeding

机译:红三叶(Trifolium pratense)育种中有用的分子标记的基因分类和挖掘

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Red clover (Trifolium pratense) is an important forage plant worldwide. This study was directed to broadening current knowledge of red clover's coding regions and enhancing its utilization in practice by specific reanalysis of previously published assembly. A total of 42,996 genes were characterized using Illumina paired-end sequencing after manual revision of Blast2GO annotation. Genes were classified into metabolic and biosynthetic pathways in response to biological processes, with 7,517 genes being assigned to specific pathways. Moreover, 17,727 enzymatic nodes in all pathways were described. We identified 6,749 potential microsatellite loci in red clover coding sequences, and we characterized 4,005 potential simple sequence repeat (SSR) markers as generating polymerase chain reaction products preferentially within 100–350 bp. Marker density of 1 SSR marker per 12.39 kbp was achieved. Aligning reads against predicted coding sequences resulted in the identification of 343,027 single nucleotide polymorphism (SNP) markers, providing marker density of one SNP marker per 144.6 bp. Altogether, 95 SSRs in coding sequences were analyzed for 50 red clover varieties and a collection of 22 highly polymorphic SSRs with pooled polymorphism information content >0.9 was generated, thus obtaining primer pairs for application to diversity studies in T. pratense. A set of 8,623 genome-wide distributed SNPs was developed and used for polymorphism evaluation in individual plants. The polymorphic information content ranged from 0 to 0.375. Temperature switch PCR was successfully used in single-marker SNP genotyping for targeted coding sequences and for heterozygosity or homozygosity confirmation in validated five loci. Predicted large sets of SSRs and SNPs throughout the genome are key to rapidly implementing genome-based breeding approaches, for identifying genes underlying key traits, and for genome-wide association studies. Detailed knowledge of genetic relationships among breeding material can also be useful for breeders in planning crosses or for plant variety protection. Single-marker assays are useful for diagnostic applications.
机译:红三叶草(Trifolium pratense)是全世界重要的牧草植物。这项研究旨在通过对以前发布的程序集进行特定的重新分析,拓宽当前对红三叶草编码区的了解并提高其在实践中的利用率。手动修订Blast2GO注释后,使用Illumina配对末端测序对总共42,996个基因进行了表征。响应生物过程,基因被分为代谢和生物合成途径,其中7,517个基因被分配给特定途径。此外,描述了所有途径中的17,727个酶促节点。我们在红三叶草编码序列中鉴定了6,749个潜在的微卫星基因座,并鉴定了4,005个潜在的简单序列重复(SSR)标记,它们优先在100-350 bp之内生成聚合酶链反应产物。每12.39 kbp获得1个SSR标记的标记密度。针对预测的编码序列的比对读数导致鉴定了343,027个单核苷酸多态性(SNP)标记,提供了每144.6 bp一个SNP标记的标记密度。总共分析了编码序列中的95个SSR,分析了50个红三叶草品种,并收集了22个高度多态SSR的集合,这些多态SSR的集合多态性信息含量> 0.9,从而获得了用于对虾的多样性研究的引物对。开发了一组8,623个全基因组分布的SNP,并将其用于单个植物的多态性评估。多态信息含量范围为0至0.375。温度转换PCR已成功用于单标记SNP基因分型,以用于靶向编码序列以及已验证的五个基因座中的杂合性或纯合性确认。预测整个基因组中的大量SSR和SNP是快速实施基于基因组的育种方法,识别关键性状的基础基因以及进行全基因组关联研究的关键。对育种材料之间遗传关系的详细了解对于育种者计划杂交或保护植物品种也很有用。单标记测定可用于诊断应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号