Zhang L H, Jenssen D
Department of Genetic and Cellular Toxicology, Wallenberg Laboratory, University of Stockholm, Sweden.
Mutat Res. 1989 Jun;212(2):253-62. doi: 10.1016/0027-5107(89)90076-6.
The aim of the present investigation was to screen for rare types of spontaneously occurring mutational events in order to provide information on the organization of the mammalian genome. For this purpose a hierarchical sequence of analyses is used with a first step utilizing a forward reverse mutation approach. The present paper deals with the characterization of 22 isolated mutants from 2 groups, 11 spontaneously appearing mutants and, in comparison, 11 ethyl methanesulfonate-induced mutants at the HPRT locus in V79 Chinese hamster cells, by means of reverse mutation analyses using selection with medium containing L-azaserine. Nine out of the 11 mutant clones of each group could be reverted either spontaneously or induced by treatments with ethyl nitrosourea (ENU), ICR191 or 5-azacytidine (5AC), which indicates that they were caused by point mutations. Two of the revertible mutant clones of spontaneous origin were found to be resistant to HAT but not HAsT medium. These 2 6TGrHATr mutants were the only mutants isolated which could be affected by 5AC with a significant increase in reversion frequency. Chromosome aberration analysis did not indicate any enhancement in aberration frequency in the X-chromosome by 5AC treatment. Studies on the mutagenicity at the OUA locus indicated that the 5AC- and ENU-induced mutation frequencies in these 2 mutants were comparable to the effects in the parent wild-type cell line. Their cellular incorporation of 3H-hypoxanthine was enhanced in the presence of aminopterin, but decreased with L-azaserine indicating that they were phosphoribosyl pyrophosphate (PRPP) mutants. On the basis of these results, it is hypothesized that reversion of these 2 6TGrHATr mutants may occur by a gene amplification mechanism and that this process may be facilitated by 5AC treatment.
本研究的目的是筛选罕见的自发突变事件类型,以便提供有关哺乳动物基因组组织的信息。为此,采用了一种分层分析序列,第一步使用正向-反向突变方法。本文通过使用含L-氮杂丝氨酸的培养基进行选择的反向突变分析,对来自2组的22个分离突变体进行了表征,其中11个是自发出现的突变体,相比之下,11个是在V79中国仓鼠细胞的次黄嘌呤-鸟嘌呤磷酸核糖转移酶(HPRT)位点由甲磺酸乙酯诱导产生的突变体。每组11个突变克隆中的9个可以自发回复突变,或者通过用亚硝基脲(ENU)、ICR191或5-氮杂胞苷(5AC)处理诱导回复突变,这表明它们是由点突变引起的。发现2个自发起源的可回复突变克隆对HAT培养基有抗性,但对HAsT培养基没有抗性。这2个6TGrHATr突变体是仅有的分离到的可受5AC影响且回复突变频率显著增加的突变体。染色体畸变分析未表明5AC处理会使X染色体的畸变频率有任何增加。对乳清酸核苷(OUA)位点的致突变性研究表明,这2个突变体中5AC和ENU诱导的突变频率与亲本野生型细胞系中的效应相当。在氨基蝶呤存在的情况下,它们对3H-次黄嘌呤的细胞摄取增强,但在L-氮杂丝氨酸存在时降低,这表明它们是磷酸核糖焦磷酸(PRPP)突变体。基于这些结果,推测这2个6TGrHATr突变体的回复突变可能通过基因扩增机制发生,并且该过程可能由5AC处理促进。