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通过变性梯度凝胶电泳印迹法在经X射线转化的小鼠10T1/2细胞中寻找癌基因突变。

Search for oncogene mutations in X-ray-transformed mouse 10T1/2 cells by denaturing gradient gel electrophoresis blotting.

作者信息

Krolewski B, Little J B

机构信息

Laboratory of Radiobiology, Harvard School of Public Health, Boston, MA 02115.

出版信息

Int J Radiat Biol. 1994 Feb;65(2):147-56. doi: 10.1080/09553009414550181.

Abstract

We have sought evidence for possible mutations within the c-myc, c-Ha-ras and c-Ki-ras loci of X-ray-transformed mouse C3H10T1/2 cell clones using the denaturing gradient gel electrophoresis (DGGE) blot technique. This highly sensitive method was developed to detect any mutations (e.g. single base changes, small deletions) in genomic DNA, by measuring differences in the melting behaviour of short DNA fragments (50-800 bp) obtained by digestion of genomic DNA with several specific 4 bp recognition site restriction enzymes. In this study, genomic DNAs derived from 23 X-ray-transformed clones were digested with several restriction enzymes, electrophorezed on denaturing gradient gel and hybridized to c-myc, c-Ha-ras and c-Ki-ras cDNA probes. No alterations in melting patterns were observed for any of these oncogenes as compared with DNA from 18 control, non-irradiated wild-type 10T1/2 cell clones, suggesting that transformation was not associated with mutation of these genes nor with changes in their patterns of methylation. However, our screening of the large portion of exons 2 and 3 of c-myc as well as of exons 1 and 2 of c-Ha-ras gene cannot exclude the possibility that some sequence differences in the high melting domains of examined fragments were not detected by this assay.

摘要

我们利用变性梯度凝胶电泳(DGGE)印迹技术,寻找X射线转化的小鼠C3H10T1/2细胞克隆的c-myc、c-Ha-ras和c-Ki-ras基因座内可能存在的突变证据。这种高灵敏度方法的开发目的是,通过测量用几种特定的4碱基识别位点限制酶消化基因组DNA后获得的短DNA片段(50 - 800 bp)熔解行为的差异,来检测基因组DNA中的任何突变(如单碱基变化、小缺失)。在本研究中,用几种限制酶消化来自23个X射线转化克隆的基因组DNA,在变性梯度凝胶上进行电泳,并与c-myc、c-Ha-ras和c-Ki-ras cDNA探针杂交。与来自18个对照、未辐照的野生型10T1/2细胞克隆的DNA相比,这些癌基因中的任何一个均未观察到熔解模式的改变,这表明转化与这些基因的突变或其甲基化模式的改变无关。然而,我们对c-myc基因第2和3外显子的大部分以及c-Ha-ras基因第1和2外显子的筛选,不能排除本检测未检测到所检查片段高熔解结构域中某些序列差异的可能性。

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