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Construction of a metastasis-associated gene subtracted cDNA library of human colorectal carcinoma by suppression subtraction hybridization

机译:抑制消减杂交技术构建大肠癌转移相关基因消减cDNA文库

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AIM: To construct a differentially-expressed gene subtracted cDNA library from two colorectal carcinoma (CRC) cell lines with different metastatic phenotypes by suppression subtractive hybridization. METHODS: Two cell lines of human CRC from the same patient were used. SW620 cell line showing highly metastatic potential was regarded as tester in the forward subtractive hybridization, while SW480 cell line with lowly metastatic potential was treated as tester in the reverse hybridization. Suppression subtractive hybridization (SSH) was employed to obtain cDNA fragments of differentially expressed genes for the metastasis of CRC. These fragments were ligated with T vectors, screened through the blue-white screening system to establish cDNA library. RESULTS: After the blue-white screening, 235 white clones were picked out from the positive-going hybridization and 232 from the reverse. PCR results showed that 200-700 bp inserts were seen in 98% and 91% clones from the forward and reverse hybridizations, respectively. CONCLUSIONS: A subtractive cDNA library of differentially expressed genes specific for metastasis of CRC can be constructed with SSH and T/A cloning techniques.
机译:目的:通过抑制性消减杂交法从两个具有不同转移表型的结直肠癌(CRC)细胞系中构建差异表达基因消减cDNA文库。方法:使用来自同一患者的两种人CRC细胞系。在正向消减杂交中显示出高转移潜力的SW620细胞系被视为测试者,而在反向杂交中将具有低转移性的SW480细胞系视为测试者。使用抑制消减杂交(SSH)获得差异表达基因的cDNA片段,用于CRC的转移。将这些片段与T载体连接,通过蓝白色筛选系统筛选以建立cDNA文库。结果:经过蓝白筛选后,从正向杂交中筛选出235个白色克隆,从反向杂交中筛选出232个白色克隆。 PCR结果表明,在正向和反向杂交中98%和91%的克隆中分别看到200-700 bp的插入片段。结论:可以通过SSH和T / A克隆技术构建特异性针对CRC转移的差异表达基因的消减cDNA文库。

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