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用于扩增寡毛纲(环节动物门)内部转录间隔区的新型特异性引物。

New specific primers for amplification of the Internal Transcribed Spacer region in Clitellata (Annelida).

作者信息

Liu Yingkui, Erséus Christer

机构信息

Department of Biological and Environmental Sciences University of Gothenburg Göteborg Sweden.

出版信息

Ecol Evol. 2017 Oct 31;7(23):10421-10439. doi: 10.1002/ece3.3212. eCollection 2017 Dec.

DOI:10.1002/ece3.3212
PMID:29238565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5723599/
Abstract

Nuclear molecular evidence, for example, the rapidly evolving Internal Transcribed Spacer region (ITS), integrated with maternally inherited (mitochondrial) COI barcodes, has provided new insights into the diversity of clitellate annelids. PCR amplification and sequencing of ITS, however, are often hampered by poor specificity of primers used. Therefore, new clitellate-specific primers for amplifying the whole ITS region (ITS: 29F/1084R) and a part of it (ITS2: 606F/1082R) were developed on the basis of a collection of previously published ITS sequences with flanking rDNA coding regions. The specificity of these and other ITS primers used for clitellates were then tested in silico by evaluating their mismatches with all assembled and annotated sequences (STD, version r127) from EMBL, and the new primers were also tested in vitro for a taxonomically broad sample of clitellate species (71 specimens representing 11 families). The in silico analyses showed that the newly designed primers have a better performance than the universal ones when amplifying clitellate ITS sequences. In vitro PCR and sequencing using the new primers were successful, in particular, for the 606F/1082R pair, which worked well for 65 of the 71 specimens. Thus, using this pair for amplifying the ITS2 will facilitate further molecular systematic investigation of various clitellates. The other pair (29F/1084R), will be a useful complement to existing ITS primers, when amplifying ITS as a whole.

摘要

例如,核分子证据,即快速进化的内转录间隔区(ITS),与母系遗传的(线粒体)细胞色素氧化酶亚基I(COI)条形码相结合,为寡毛纲环节动物的多样性提供了新的见解。然而,ITS的PCR扩增和测序常常受到所用引物特异性差的阻碍。因此,基于一系列先前发表的带有侧翼rDNA编码区的ITS序列,开发了用于扩增整个ITS区域(ITS:29F/1084R)及其一部分(ITS2:606F/1082R)的新的寡毛纲特异性引物。然后,通过评估这些引物和用于寡毛纲的其他ITS引物与来自EMBL的所有组装和注释序列(STD,版本r127)的错配情况,在计算机上对其特异性进行了测试,并且还针对寡毛纲物种的广泛分类样本(代表11个科的71个标本)对新引物进行了体外测试。计算机分析表明,在扩增寡毛纲ITS序列时,新设计的引物比通用引物具有更好的性能。使用新引物进行的体外PCR和测序取得了成功,特别是对于606F/1082R引物对,该引物对在71个标本中的65个中效果良好。因此,使用该引物对扩增ITS2将有助于对各种寡毛纲进行进一步的分子系统研究。另一对引物(29F/1084R)在扩增整个ITS时,将是现有ITS引物的有用补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/5723599/459f89eeaf38/ECE3-7-10421-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/5723599/ca7180d173ef/ECE3-7-10421-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/5723599/013567856094/ECE3-7-10421-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/5723599/459f89eeaf38/ECE3-7-10421-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/5723599/ca7180d173ef/ECE3-7-10421-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/5723599/013567856094/ECE3-7-10421-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/5723599/459f89eeaf38/ECE3-7-10421-g003.jpg

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