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基于AT/AAT多态性重复序列的微卫星多态性位点改良选择性扩增技术对新基因组图谱进行电泳鉴定。

Electrophoretic identification of new genomic profiles with a modified selective amplification of microsatellite polymorphic loci technique based on AT/AAT polymorphic repeats.

作者信息

Palacios Gustavo, Bustamante Silvia, Molina Carlos, Winter Peter, Kahl Günter

机构信息

Plant Biotechnology Laboratory, Central University of Venezuela, Caracas, Venezuela.

出版信息

Electrophoresis. 2002 Sep;23(19):3341-5. doi: 10.1002/1522-2683(200210)23:19<3341::AID-ELPS3341>3.0.CO;2-C.

Abstract

The present paper introduces improvements of the conventional selective amplification of microsatellite polymorphic loci (SAMPL) technique, that exploit AT-rich microsatellite primers. Generally, AT/AAT microsatellites are frequent components of eukaryotic genomes, but their ubiquity and polymorphic information content (PIC) could not be exploited yet, because standard SAMPL conditions did not allow amplifications. Here we report (i) on the design of new versatile AT-rich microsatellite primers, that are combined with (ii) a modified SAMPL adapter primer (called EcoRI-Short), and (iii) special polymerase chain reaction (PCR) amplification regimes. The novel SAMPL procedure expands the range of useful microsatellite primers to AT-rich sequences and produces a high number of bands and a clear banding pattern, and detects polymorphisms in otherwise nonpolymorphic genomes of plants (Dioscorea alata, D. rotundata) and a fungus (Mycosphaerella fijiensis).

摘要

本文介绍了对传统微卫星多态性位点选择性扩增(SAMPL)技术的改进,该技术利用富含AT的微卫星引物。一般来说,AT/AAT微卫星是真核生物基因组的常见组成部分,但由于标准SAMPL条件不允许扩增,其普遍性和多态信息含量(PIC)尚未得到利用。在此,我们报告:(i)新型通用富含AT微卫星引物的设计,该引物与(ii)改良的SAMPL衔接子引物(称为EcoRI-Short)以及(iii)特殊的聚合酶链反应(PCR)扩增方案相结合。这种新型SAMPL程序将有用的微卫星引物范围扩展到富含AT的序列,产生大量条带和清晰的条带模式,并在植物(参薯、圆果黄独)和一种真菌(香蕉叶斑病菌)原本无多态性的基因组中检测到多态性。

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