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一个在自发性高血压大鼠和Wistar-Kyoto大鼠基因组之间呈现限制性片段长度多态性的DNA片段的克隆。

Cloning of a DNA fragment displaying restriction fragment length polymorphisms between the genomes of spontaneously hypertensive and Wistar-Kyoto rats.

作者信息

Yagisawa H, Kambe T, Nojima H

机构信息

Department of Medical Biology, Jichi Medical School, Tochigi-ken, Japan.

出版信息

J Hypertens. 1990 Apr;8(4):307-13. doi: 10.1097/00004872-199004000-00003.

Abstract

A 3 kilobase (kb) EcoRI fragment cloned from the genome of the spontaneously hypertensive rat (SHR) displayed restriction fragment length polymorphism (RFLP) compared with the genome of the Wistar-Kyoto rat (WKY) when total genomic Southern blot analysis was performed for two restriction enzymes, PstI and PvuII. Sequencing of the DNA fragment cloned from genomic SHR and WKY libraries revealed that this 3 kb EcoRI fragment harbours three point mutations. Two of them (C to T and A to T) are situated in the middle of the restriction sites for PstI and PvuII, thus disrupting the recognition sites for these enzymes in the SHR genome. Southern blot analysis using total complementary (c) DNA obtained from cDNA libraries of aortic smooth muscle cells from SHR and a whole WKY kidney, with this 3 kb EcoRI fragment as a probe, showed polymorphic bands suggesting that these point mutations are reflected in the sequences of messenger (m) RNA transcribed from the gene encoded in this 3 kb fragment. Detection of two bands by a Northern blot analysis for RNA from various SHR tissues indicates that this 3 kb fragment is actively transcribed in vivo.

摘要

当使用两种限制性内切酶PstI和PvuII对基因组进行Southern印迹分析时,从自发性高血压大鼠(SHR)基因组中克隆的一个3千碱基(kb)的EcoRI片段与Wistar-Kyoto大鼠(WKY)的基因组相比,显示出限制性片段长度多态性(RFLP)。对从SHR和WKY基因组文库中克隆的DNA片段进行测序后发现,这个3 kb的EcoRI片段含有三个点突变。其中两个(C突变为T和A突变为T)位于PstI和PvuII的限制性酶切位点中间,从而破坏了SHR基因组中这些酶的识别位点。以这个3 kb的EcoRI片段为探针,对从SHR主动脉平滑肌细胞cDNA文库和整个WKY肾脏获得的总互补(c)DNA进行Southern印迹分析,结果显示出多态性条带,这表明这些点突变反映在由这个3 kb片段编码的基因转录的信使(m)RNA序列中。对来自各种SHR组织的RNA进行Northern印迹分析检测到两条带,这表明这个3 kb的片段在体内被活跃转录。

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