以γ射线诱发转化的大鼠胚胎细胞(REC:myc:γ33)的DNA构建粘粒基因库,用总基因库DNA转染NIH/3T3细胞,产生转化灶的DNA作二轮转染,二轮转化的NIH/3T3细胞内有大鼠REC:myc:γ33DNA中具转化活性的N-ras基因,用不对称PCR和DNA序列分析法证明,REC:myc:γ33细胞中鼠N-ras的活化是由于第61位密码子的A→G点突变.NIH/3T3转化灶中鼠N-ras也有同样点突变,但NIH/3T3细胞的内源性N-ras基因则无此突变.
A cosmid library,constructed from DNA of the γ-radiation-transformed REC: myc cell line, designated REC:myc:γ33.was transfected into NIH/3T3 cells,yielding foci.Another round transfection of DNA from the first round focus into fresh NIH/3T3 cells produced second round foci.An active N-ras gene which originated from rat REC: myc:γ33 cells was detected in the NIH/3T3 secondary transformants.With PCR and direct DNA sequencing techniques,rat N-ras gene was found activated in the REC:myc:γ33 cells by CAA→CGA point mutation at codon 61, but not in the REC:myc cells. Also rat N-ras gene was identified as a point mutated gene in the NIH/3T3 transformants, and the endogenous N-ras gene in the NIH/3T3 recipient cells remains normal. What was found to be more interesting is that five out of six γ-radiation transformed REC:myc cell lines bear the same point mutation (CAA→CGA) indicating association of γ-radiation-induced transformation with point mutation in the N-ras gene.
陈昌虎,姚开泰,C. C. LING.γ射线诱发大鼠胚胎细胞转化与N-ras的激活[J].生物化学与生物物理进展,1994,21(3):228-234
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