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快速简便筛选cDNA文库的SSS法 被引量:7

SSS Method for Screening cDNA Library
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摘要 建立了一种快速简便筛选cDNA文库的方法—SSS法(subsectionscreening)。该方法用cDNA噬菌体平板划块分组和根据目的基因设计的一对特异性引物,用PCR技术逐级筛选cDNA文库获得目的基因。与其它筛选cDNA文库的方法相比,该方法范围可控,目标明确,易于获得目的基因,而且快速、简捷、省时,一般可在一周内筛选出目的基因。本实验室利用该方法在半个月内筛选出了一个查耳酮异构酶(chalconeisomerase)(CHI)基因,一个黄酮类化合物3′ 羟化酶(flavonoid3′hydroxylase)(F3′H)基因,一个热激蛋白(heatshockprotein)(HSP)基因和一个1484bp热激蛋白基因片段。此方法用于同时筛选多个基因,可收到事半功倍的效果,对其它文库筛选也有借鉴意义。 A quick and simple method subsection screening (SSS) method for screening cDNA library by PCR was established.With this method,cDNA phage plate was cut into several blocks and a couple of primers was designed according to target gene.And then the target genes were obtained by screening cDNA library.Comparing with other methods,this method has many advantages such as controlled range and clear target,and also quick and simple for obtaining the target genes.It is possible to get a target gene in one week in general by this method.Thus,the CHI gene,F3′H gene,HSP gene and one HSP partial fragment,were obtained respectively in half month in our lab.We can get twice the result with half the effort when we screen several genes in the same time.It is also suitable to screen other libraries.
出处 《遗传》 CAS CSCD 北大核心 2003年第5期583-586,共4页 Hereditas(Beijing)
基金 国家自然科学基经项目(No.:39970896) 中科院知识创新项目(No.:KSCXI-09)
关键词 SSS法 CDNA文库 PCR 文库筛选 subsection screening method cDNA library PCR library screening
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  • 1[1]Searles L L,Jokerst R S,Binghham P M,Voelker R A, Greenleaf A L.Molecular cloning of sequences from a drosophila RNA polymerase Ⅱ locus by P element transposon tagging[J].Cell,1982,31:585.
  • 2[2]Lisitsyn Ni,Lisitsyn Na,Wigler M.Cloning the differences between two complex genomes[J].Science,1993,259(12):946~951.
  • 3[3]Liang P,Pardee A B.Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction[J].Science,1992,257(14):967~971.
  • 4[4]Song W Y,Wang G L,Chen L L,Kim H S,Pi L Y,Holsten T,Gardner J,Wang B,Zhai W X,Zhu L H,Fanquet C,Ronald P C.A receptor kinase-like protein encoded by the rice disease resistance gene,Xa21[J].Science,1995,270:1804.
  • 5[5]Benton W D,Davis R W.Screening λgt Recombinant clones by hybridization to single plaques in situ[J].Science,1977,196:180.
  • 6[6]Amaravadi L,King M W.A rapid and efficient nonradioactive method for screening recombinant DNA libraries[J].Biotechniques,1994,16(1):98~103.
  • 7[7]Carl W Dieffenbach,Gabriela S.Dveksler PCR primer:A laboratory manual[M].Cold Spring Harbor Laboratory Press,1995.

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