Käfer E
Mutat Res. 1986 Jun;164(3):145-66. doi: 10.1016/0165-1161(86)90006-3.
A system of tests with the ascomycete Aspergillus nidulans was devised that can detect 3 primary effects of genotoxic agents: (1) increases in mitotic crossing-over; (2) induced aneuploidy; and (3) clastogenic effects which cause chromosomal imbalance. Conidia of a new diploid tester strain, heterozygous for 4 recessive markers which alter conidial color, are treated and plated onto nonselective media. In cases of induced crossing-over, large color segments are found in normal green colonies, frequently adjacent to reciprocal twin segments. In contrast, both malsegregation and chromosome breakage produce unbalanced types which grow poorly and segregate further. Cases with yellow segregants are replated and their secondary diploid sectors tested for markers which are located on both chromosome arms in coupling with yA. Induced aneuploidy can be distinguished from chromosome breakage by the pattern of marker segregation. Any aneuploid type will produce euploid sectors solely by segregation of whole chromosomes; trisomic colonies (yA / yA / +) will show 1:2 ratios for yellow (homozygous yA) to parental green (yA/+) sectors and have characteristic phenotypes. Other induced unbalanced types, if heterozygous for deletions or aberrations may produce yellow diploid sectors by secondary crossing-over as well as by nondisjunction and such cases show unique patterns of genetic segregation and non- predictable phenotypes. As a complementary test, haploid strains are treated and induced abnormally growing types are replated and classified by phenotype. Aneuploids are unstable and produce many normal sectors, and some of these disomic or trisomic types can be visually identified.In contrast, induced deletions are lethal, and duplications or 'morphological' mutants show much more stable abnormal phenotypes. This test system was used to characterize the primary effects of gamma-rays and chloral hydrate. Results and evidence were as follows: (1) A dose-dependent increase of color segments resulting from reciprocal crossing-over was found after treatment of dividing nuclei in germinating diploid conidia with gamma-rays, but not with chloral hydrate. (2) Highly aneuploid and polyploid types were induced in diploid and haploid germinating conidia by chloral hydrate but not to any significant extent by gamma-rays. (3) gamma-Rays caused a dose- dependent increase off abnormally growing colonies when dormant or germinating diploid conidia were treated. These colonies produced secondary euploid sectors by spontaneous nondisjunction and frequently also by crossing-over, which provided evidence for induced semidominant and recessive lethal mutations of many types.
设计了一种使用构巢曲霉的测试系统,该系统可检测遗传毒性剂的3种主要效应:(1)有丝分裂交换增加;(2)诱导非整倍体;(3)导致染色体不平衡的断裂效应。将一种新的二倍体测试菌株的分生孢子进行处理,该菌株对4个改变分生孢子颜色的隐性标记杂合,然后接种到非选择性培养基上。在诱导交换的情况下,在正常绿色菌落中发现大的颜色区段,通常与相互的双区段相邻。相比之下,错误分离和染色体断裂都会产生生长不良并进一步分离的不平衡类型。出现黄色分离株的情况重新接种,并对其次级二倍体区段进行与yA连锁的位于两条染色体臂上的标记测试。诱导的非整倍体可以通过标记分离模式与染色体断裂区分开来。任何非整倍体类型仅通过整条染色体的分离就会产生整倍体区段;三体菌落(yA / yA / +)黄色(纯合yA)与亲本绿色(yA / +)区段的比例将显示为1:2,并且具有特征性表型。其他诱导的不平衡类型,如果对缺失或畸变杂合,可能通过二次交换以及不分离产生黄色二倍体区段,并且这种情况显示出独特的遗传分离模式和不可预测的表型。作为补充测试,对单倍体菌株进行处理,将诱导的异常生长类型重新接种并按表型分类。非整倍体不稳定,会产生许多正常区段,其中一些二体或三体类型可以通过视觉识别。相比之下,诱导的缺失是致死的,重复或“形态学”突变体表现出更稳定的异常表型。该测试系统用于表征γ射线和水合氯醛的主要效应。结果和证据如下:(1)用γ射线处理萌发的二倍体分生孢子中的分裂核后,发现由相互交换导致的颜色区段呈剂量依赖性增加,但水合氯醛处理则未出现这种情况。(2)水合氯醛在二倍体和单倍体萌发的分生孢子中诱导出高度非整倍体和多倍体类型,但γ射线在很大程度上未诱导出此类情况。(3)当处理休眠或萌发的二倍体分生孢子时,γ射线导致异常生长菌落的剂量依赖性增加。这些菌落通过自发不分离以及频繁地通过交换产生次级整倍体区段,这为诱导多种类型的半显性和隐性致死突变提供了证据。