首页> 美国卫生研究院文献>PLoS Clinical Trials >Internal Transcribed Spacer 2 (nu ITS2 rRNA) Sequence-Structure Phylogenetics: Towards an Automated Reconstruction of the Green Algal Tree of Life
【2h】

Internal Transcribed Spacer 2 (nu ITS2 rRNA) Sequence-Structure Phylogenetics: Towards an Automated Reconstruction of the Green Algal Tree of Life

机译:内部转录间隔物2(nu ITS2 rRNA)序列结构系统发生学:走向绿色藻类生命树的自动重建。

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

BackgroundChloroplast-encoded genes (matK and rbcL) have been formally proposed for use in DNA barcoding efforts targeting embryophytes. Extending such a protocol to chlorophytan green algae, though, is fraught with problems including non homology (matK) and heterogeneity that prevents the creation of a universal PCR toolkit (rbcL). Some have advocated the use of the nuclear-encoded, internal transcribed spacer two (ITS2) as an alternative to the traditional chloroplast markers. However, the ITS2 is broadly perceived to be insufficiently conserved or to be confounded by introgression or biparental inheritance patterns, precluding its broad use in phylogenetic reconstruction or as a DNA barcode. A growing body of evidence has shown that simultaneous analysis of nucleotide data with secondary structure information can overcome at least some of the limitations of ITS2. The goal of this investigation was to assess the feasibility of an automated, sequence-structure approach for analysis of IT2 data from a large sampling of phylum Chlorophyta.
机译:背景技术叶绿体编码基因(matK和rbcL)已被正式提议用于靶向胚胎植物的DNA条形码研究。但是,将这样的协议扩展到绿藻丹绿藻时会遇到很多问题,包括非同源性(matK)和异质性,这些问题阻止了通用PCR工具包(rbcL)的创建。一些人提倡使用核编码的内部转录间隔区2(ITS2)作为传统叶绿体标记的替代方法。但是,人们普遍认为ITS2保守性不足,或者由于基因渗入或双亲遗传模式而混淆,从而使其无法广泛用于系统发育重建或作为DNA条码。越来越多的证据表明,同时分析具有二级结构信息的核苷酸数据可以克服ITS2的至少某些局限性。这项研究的目的是评估一种自动化的,序列结构的方法来分析大叶绿藻中IT2数据的可行性。

著录项

相似文献

  • 外文文献
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