de Serres F J
Center for Life Sciences and Toxicology, Chemistry and Life Sciences, Research Triangle Institute, Research Triangle Park, NC 27709.
Mutat Res. 1991 Jan;246(1):15-30. doi: 10.1016/0027-5107(91)90105-w.
In previous studies, X-ray-induced specific-locus mutations in the adenine-3 (ad-3) region of a two-component heterokaryon (H-12) of Neurospora crassa were combined with a series of tester strains carrying markers in the ad-3 and immediately adjacent regions to map mutants that were presumed multilocus deletions (de Serres, 1989c, 1990a). Two new classes of X-ray-induced mutations were recovered: multiple-locus mutations consisting of gene/point mutations at the ad-3A or ad-3B locus with a closely linked recessive lethal mutation, or multilocus deletions covering the ad-3A, ad-3B and/or nic-2 loci with a closely linked recessive lethal mutation (designated ad-3R + RLCL and [ad-3]IR + RLCL, respectively). Thus, the ad-3 specific-locus assay can detect damage occurring at the ad-3A and the ad-3B loci, as well as at a minimum of 19 other loci in the immediately adjacent regions. The original overall spectrum of ad-3 mutations can be resolved, by genetic analysis, into a series of 30 subclasses. In the present paper, the data from the genetic analysis of 832 X-ray-induced mutants recovered from a series of 4 experiments (Webber and de Serres, 1965) have been presented in terms of Mutational Spectra organized as a function of X-ray dose. Comparison of these Spectra demonstrates the shift from high percentages of gene/point mutations (with a high percentage of mutants at the ad-3B locus showing allelic complementation) at low doses, to low percentages of gene/point mutations (with a low percentage of ad-3B mutants showing allelic complementation) and high percentages of multilocus deletion mutations and multiple-locus mutations (of genotype ad-3R + RLCL or [ad-3]IR + RLCL) at high doses. These Mutational Spectra demonstrate the marked dose-dependence of X-ray-induced specific-locus mutations in a eukaryotic organism.
在先前的研究中,将粗糙脉孢菌双组分异核体(H-12)腺嘌呤-3(ad-3)区域的X射线诱导的特定基因座突变与一系列在ad-3及其紧邻区域携带标记的测试菌株相结合,以定位推测为多位点缺失的突变体(德塞雷斯,1989c,1990a)。回收了两类新的X射线诱导突变:一类是多位点突变,由ad-3A或ad-3B基因座处的基因/点突变与紧密连锁的隐性致死突变组成;另一类是覆盖ad-3A、ad-3B和/或nic-2基因座且带有紧密连锁隐性致死突变的多位点缺失(分别命名为ad-3R + RLCL和[ad-3]IR + RLCL)。因此,ad-3特定基因座检测法能够检测到在ad-3A和ad-3B基因座以及紧邻区域至少19个其他基因座处发生的损伤。通过遗传分析,最初的ad-3突变总体谱可解析为一系列30个亚类。在本文中,呈现了从一系列4个实验(韦伯和德塞雷斯,1965)中回收的832个X射线诱导突变体的遗传分析数据,这些数据以作为X射线剂量函数组织的突变谱形式呈现。这些谱的比较表明,从低剂量时高比例的基因/点突变(ad-3B基因座处高比例的突变体显示等位基因互补),转变为高剂量时低比例的基因/点突变(ad-3B突变体中低比例显示等位基因互补)以及高比例的多位点缺失突变和多位点突变(基因型为ad-3R + RLCL或[ad-3]IR + RLCL)。这些突变谱证明了真核生物中X射线诱导的特定基因座突变具有显著的剂量依赖性。