首页> 美国卫生研究院文献>Genes >New Oligonucleotide Probes for ND-FISH Analysis to Identify Barley Chromosomes and to Investigate Polymorphisms of Wheat Chromosomes
【2h】

New Oligonucleotide Probes for ND-FISH Analysis to Identify Barley Chromosomes and to Investigate Polymorphisms of Wheat Chromosomes

机译:用于ND-FISH分析的新寡核苷酸探针用于鉴定大麦染色体并研究小麦染色体的多态性

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

Oligonucleotide probes that can be used for non-denaturing fluorescence in situ hybridization (ND-FISH) analysis are convenient tools for identifying chromosomes of wheat (Triticum aestivum L.) and its relatives. New oligonucleotide probes, Oligo-HvT01, Oligo-pTa71-1, Oligo-s120.1, Oligo-s120.2, Oligo-s120.3, Oligo-275.1, Oligo-275.2, Oligo-k566 and Oligo-713, were designed based on the repetitive sequences HVT01, pTa71, pTa-s120, pTa-275, pTa-k566 and pTa-713. All these probes can be used for ND-FISH analysis and some of them can be used to detect polymorphisms of wheat chromosomes. Probes Oligo-HvT01, Oligo-pTa71-1, Oligo-s120.3, Oligo-275.1, Oligo-k566 and Oligo-713 can, respectively, replace the roles of their original sequences to identify chromosomes of some barley (Hordeum vulgare ssp. vulgare) and the common wheat variety Chinese Spring. Oligo-s120.1, Oligo-s120.2 and Oligo-275.2 produced different hybridization patterns from the ones generated by their original sequences. In addition, Oligo-s120.1, Oligo-s120.2 and Oligo-s120.3, which were derived from pTa-s120, revealed different signal patterns. Likewise, Oligo-275.1 and Oligo-275.2, which were derived from pTa-275, also displayed different hybridization patterns. These results imply that differently arranged or altered structural statuses of tandem repeats might exist on different chromosome regions. These new oligonucleotide probes provide extra convenience for identifying some wheat and barley chromosomes, and they can display polymorphisms of wheat chromosomes.
机译:可以用于非变性荧光原位杂交(ND-FISH)分析的寡核苷酸探针是鉴定小麦(Triticum aestivum L.)及其亲缘染色体的便捷工具。设计了新的寡核苷酸探针Oligo-HvT01,Oligo-pTa71-1,Oligo-s120.1,Oligo-s120.2,Oligo-s120.3,Oligo-275.1,Oligo-275.2,Oligo-k566和Oligo-713基于重复序列HVT01,pTa71,pTa-s120,pTa-275,pTa-k566和pTa-713。所有这些探针都可用于ND-FISH分析,其中一些可用于检测小麦染色体的多态性。探针Oligo-HvT01,Oligo-pTa71-1,Oligo-s120.3,Oligo-275.1,Oligo-k566和Oligo-713可以分别取代其原始序列的作用来鉴定某些大麦的染色体(Hordeum vulgare ssp。普通小麦品种和中国春。 Oligo-s120.1,Oligo-s120.2和Oligo-275.2产生了与其原始序列产生的杂交模式不同的杂交模式。另外,源自pTa-s120的Oligo-s120.1,Oligo-s120.2和Oligo-s120.3揭示了不同的信号模式。同样,衍生自pTa-275的Oligo-275.1和Oligo-275.2也显示出不同的杂交模式。这些结果暗示串联重复序列的不同排列或改变的结构状态可能存在于不同的染色体区域上。这些新的寡核苷酸探针为鉴定一些小麦和大麦染色体提供了额外的便利,并且可以显示小麦染色体的多态性。

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