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限制性内切酶标记cDNA扫描(RLCS):一种使用二维凝胶电泳的新型cDNA展示系统。

Restriction landmark cDNA scanning (RLCS): a novel cDNA display system using two-dimensional gel electrophoresis.

作者信息

Suzuki H, Yaoi T, Kawai J, Hara A, Kuwajima G, Wantanabe S

机构信息

Shionogi Institute for Medical Science, Osaka, Japan.

出版信息

Nucleic Acids Res. 1996 Jan 15;24(2):289-94. doi: 10.1093/nar/24.2.289.

Abstract

We have developed a new method, designated restriction landmark cDNA scanning (RLCS), which displays many cDNA species quantitatively and simultaneously as two-dimensional gel spots. In this method cDNA species of uniform length were prepared for each mRNA species using restriction enzymes. After the restriction enzyme sites were radiolabeled as landmarks, the labeled fragments were subjected to high resolution two-dimensional gel electrophoresis. In analyses of cDNA samples from adult mouse liver and brain (cerebral cortex, cerebellum and brain stem) we detected approximately 500 and >1000 discrete gel spots respectively of various intensities at a time. The spot patterns of the three brain regions were very similar, although not identical, but were quite different from the pattern for the liver. RNA blot hybridization analysis using several cloned spot DNAs as probes showed that differences in intensity of the spots among RLCS profiles correlated well with expression levels of the corresponding mRNA species in the brain regions. Because the spots and their intensities reflect distinct mRNA species and their expression level respectively, the RLCS is a novel cDNA display system which provides a great deal of information and should be useful for systematic documentation of differentially expressed genes.

摘要

我们开发了一种新方法,称为限制性内切酶标记cDNA扫描(RLCS),它能将许多cDNA种类作为二维凝胶斑点进行定量且同时显示。在该方法中,使用限制性内切酶为每个mRNA种类制备长度一致的cDNA种类。在将限制性酶切位点作为标记进行放射性标记后,将标记的片段进行高分辨率二维凝胶电泳。在对成年小鼠肝脏和大脑(大脑皮层、小脑和脑干)的cDNA样本分析中,我们一次分别检测到约500个和超过1000个不同强度的离散凝胶斑点。三个脑区的斑点模式非常相似,虽不完全相同,但与肝脏的模式有很大差异。使用几种克隆的斑点DNA作为探针进行RNA印迹杂交分析表明,RLCS图谱中斑点强度的差异与脑区中相应mRNA种类的表达水平密切相关。由于斑点及其强度分别反映了不同的mRNA种类及其表达水平, RLCS是一种新型的cDNA显示系统,可提供大量信息,应有助于对差异表达基因进行系统记录。

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