Regulation of gene expression is one of the most importa nt responses of cells to DNA damage induced by radiation. A novel expressed seq u ence tag (EST) fragment had been cloned from human embryo lung cells induced by 50cGy radiation and named RIG1. To clone the full-length cDNA of RIG1, a non-c loned cDNA library of human embryo lung cells induced by low dose irradiation ha d been established. This library was used as template in enchanced nest RACE PCR and biotin-labeled probe was used for further purification. The 3′ flanking s equence of this EST was cloned and sequenced with this set of technology. It was illuminated by homology analysis that this 3′ flanking sequence and the origin al EST are well aligned with a BAC clone of 20th chromosome and the predic ted exons sequence of this chromosome is well consisten ce with the real EST. Thus the RIG1 can be roughly located in 20th chromos ome. By use of the exons sequence predicted from chromosome sequence by GENSCA N, full-length of RIG1 gene has been cloned. Chromosome location of RIG1 gene i s further determined by this successful verification of Bioinformatics predictio n by experiment. By the same step, genome sequence of RIG1 has been determined. Therefore,by the combined use of Bioinformatics analysis，the full-length cDNA sequence and genome sequence of RIG1 gene are obtained and the predicted protei n sequence is determined.%研究辐射诱导的基因表达调控对于认识细胞对辐射损伤的应激反应有重要意 义.在低剂量辐射诱导新基因RIG1表达序列标签(expression sequence tag,EST)片段的基础 上，通过非克 隆cDNA文库和RACE(rapid amplification of cDNA end)技术获得了其3′末端.依据实验得 到的这两段EST序列所提供的信息，通过生物信息学分析将RIG1基因初步定位在20号染色体. 对20号染色体RIG1区基因组序列进行外显子扫描，发现预测的外显子正好与实验得到的 EST相吻合.利用预测的外显子设计特异引物，成功地克隆了RIG1基因全长序列.同时，对2 0号染色体RIG1区的生物信息学分析表明，在RIG1基因的上游存在启动子区，从而确定了RIG 1基因的基因组序列.因此，通过生物信息学辅助设计实验，快捷地定位及延伸了未知EST片 段RIG1，基本完成了RIG1的全基因、基因组序列及染色体定位研究.
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