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粗糙脉孢菌两组分异核体ad-3区域的X射线诱导特异性位点突变。IV. 基因型为ad-3A和ad-3B的不可修复突变体源自多位点缺失和意外高频率的多位点突变。

X-ray-induced specific-locus mutations in the ad-3 region of two-component heterokaryons of Neurospora crassa. IV. Irreparable mutants of genotype ad-3A and ad-3B result from multilocus deletion and an unexpectedly high frequency of multiple-locus mutations.

作者信息

de Serres F J

机构信息

Center for Life Sciences and Toxicology, Research Triangle Institute, Research Triangle Park, NC 27709.

出版信息

Mutat Res. 1989 Oct;214(2):297-319. doi: 10.1016/0027-5107(89)90173-5.

Abstract

The induction of specific-locus mutations in the ad-3 region of Neurospora crassa after X-irradiation was studied in a two-component heterokaryon to determine: (1) the ratio of reparable ad-3 mutants (presumed gene/point mutations, designated ad-3R) to irreparable ad-3 mutants (presumed multilocus deletions, designated ad-3IR), and (2) the induction kinetics of each class (Webber and de Serres, 1965). More extensive genetic tests made subsequently (de Serres, 1989a) on the 832 X-ray-induced specific-locus mutations recovered in those experiments showed that unexpected high frequencies of reparable and irreparable ad-3 mutants are actually multiple-locus mutants that have additional, but separate, sites of recessive lethal (RLCL) damage in the immediately adjacent genetic regions (designated ad-3R + RLCL or ad-3IR + RLCL). The frequencies of these X-ray-induced multiple-locus mutants in the ad-3 region are orders of magnitude higher than expected on the basis of target theory (where the frequency of the double mutant is expected to be the product of the frequencies of each single mutant) and classical models of chromosome structure during interphase (de Serres, 1989a). In the present paper, a random sample of 832 X-ray-induced ad-3 mutants of genotype ad-3A or ad-3B that are irreparable have been subjected to more extensive genetic fine-structure analysis. These experiments were designed to determine the extent of the functional inactivation in individual mutants in the ad-3 and immediately adjacent genetic regions in mutants classified as presumptive multilocus deletions or multiple-locus mutations. These experiments have shown that in Neurospora crassa most X-ray-induced irreparable mutants of genotype ad-3A or ad-3B map as a series of overlapping multilocus deletions. Among the 29 irreparable mutants of genotype ad-3A, there are 16 different subgroups of complementation patterns; and among the 63 irreparable mutants of genotype ad-3B, there are also 16 different subgroups. In addition, mutants classified as presumptive multiple-locus mutants result from a variety of separate, but closely linked, sites of genetic damage.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在一个双组分异核体中研究了粗糙脉孢菌X射线照射后ad - 3区域特定位点突变的诱导情况,以确定:(1)可修复的ad - 3突变体(推测为基因/点突变,称为ad - 3R)与不可修复的ad - 3突变体(推测为多位点缺失,称为ad - 3IR)的比例,以及(2)每类突变体的诱导动力学(韦伯和德塞雷斯,1965年)。随后(德塞雷斯,1989a)对在那些实验中回收的832个X射线诱导的特定位点突变进行了更广泛的遗传测试,结果表明,可修复和不可修复的ad - 3突变体出现意外高频率,实际上是多位点突变体,在紧邻的遗传区域有额外但独立的隐性致死(RLCL)损伤位点(称为ad - 3R + RLCL或ad - 3IR + RLCL)。在ad - 3区域,这些X射线诱导的多位点突变体的频率比基于靶标理论(其中双突变体的频率预计为每个单突变体频率的乘积)和间期染色体结构经典模型所预期的高几个数量级(德塞雷斯,1989a)。在本文中,对832个基因型为ad - 3A或ad - 3B的X射线诱导的不可修复的ad - 3突变体进行了随机抽样,进行了更广泛的遗传精细结构分析。这些实验旨在确定在被归类为推测的多位点缺失或多位点突变的突变体中,ad - 3及紧邻遗传区域中各个突变体的功能失活程度。这些实验表明,在粗糙脉孢菌中,大多数基因型为ad - 3A或ad - 3B的X射线诱导的不可修复突变体定位为一系列重叠的多位点缺失。在29个基因型为ad - 3A的不可修复突变体中,有16个不同的互补模式亚组;在63个基因型为ad - 3B的不可修复突变体中,也有16个不同的亚组。此外,被归类为推测的多位点突变体是由各种独立但紧密连锁的遗传损伤位点导致的。(摘要截选至400字)

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