Interaction between chemical mutagens with a delayed effect and metabolites of seeds

Summary A study was made of chromosome aberrations in Crepis capillaris seedlings, induced by the reaction products of chemical mutagens with seed metabolites. Interaction between ethylenimine and seed metabolites of some plants of the family Compositae (C. capillaris, Taraxacum officinale, Pyrethrum carneum, Helianthus annuus) has been found to lead to the formation of highly active secondary mutagens whose action remains similar to that of ethylenimine, although the effect of ethylenimine is enhanced dozens of times. The substances responsible for this enhancement effect are contained in the fruit coating of the seed. The metabolites of seeds of other plants studied (Triticum vulgare, Hordeum vulgare, Fagopyrum esculentum) enhanced the effect of ethylenimine only 1.5–2.0 times. Unlike ethylenimine, the effect of its derivatives (thioTEP and phosphazine) and of ethyl methanesulphonate, HN2 and maleic hydrazide is not enhanced after their interaction with metabolites of compositae plant seeds. Experiments with HN2 revealed an almost complete inactivation of the mutagenic action of NH2 by metabolites of C. capillaris seeds. The observed modification of the mutagenic action of ethylenimine and NH2 after successive treatment of seedlings with mutagens and metabolites of seeds points to the preservation of the mutagen in the cell. It is concluded that when chemical mutagens act on the cells, chromosome aberrations are induced not only by the chemical agent itself, but also by its reaction with cell metabolites.     

Interaction between chemical mutagens with a delayed effect and metabolites of seeds

Summary A study was made of the cytogenetic effect of mutagens with a delayed effect (ethylenimine and ethyl methanesulphonate) on Crepis capillaris seeds. The effect was found to depend on the physiological condition of the seeds. In seeds not subjected to prolonged storage, where only chromatid aberrations were occurring spontaneously, mutagens also induced chromatid aberrations only. If, however, because of physiological changes in the seeds (e.g. upon prolonged storage or when seeds were kept at an elevated temperature and humidity) a large number of chromosome-type aberrations appeared, they also appeared when the seeds were acted upon by mutagens with a delayed effect. The action of such mutagens was also found to depend on spontaneous mutation in seeds with different rates of germination. Special experiments showed that the interaction of ethylenimine with the metabolites of seeds in vitro leads to the formation of secondary active mutagens differing from ethylenimine in the nature of their action. The induction of chromosome-type aberrations by treating seeds with alkylating compounds may be due to the action of secondary mutagens.     

A search for chromosome aberrations induced in mouse spermatogonia by chemical mutagens

Two established chemical mutagens—ethylmethanesulphonate (EMS) and triethylenemelamine (TEM)—were tested for the ability to induce chromosome aberrations in mouse spermatogonia. While not a single aberration was detected following the EMS treatment, a low frequency of translocations and fragments was found in the TEM groups. These findings are in agreement with the data obtained with the specific locus mutation test as applied to male mouse premeiotic germ cells but contrast with the effectiveness of these chemicals in breaking chromosomes in male mouse postmeiotic germ cells. A differential sensitivity of post- and premeiotic germ cells to any kind of genetic damage by these chemical mutagens is most likely to be the correct interpretation of all the data. However, it is also suggested that a high proportion of translocations induced in spermatogonia by chemical mutagens may not be detectable by present methods.     

Induction of chromosome aberrations by chemical mutagens in neural ganglia of Drosophila melanogaster

Chromatid aberrations induced by various concentrations of bleomycin, cyclophosphamide and mitomycin C were analyzed in neural ganglia of third-instar larvae of Drosophila melanogaster. A clear dose response was observed with increasing dose after treatment with bleomycin and mitomycin C, whereas no effect was observed after treatment with cyclophosphamide. A comparison with published data for the induction of sex-linked recessive lethals showed that, at least for the 3 drugs tested, the use of both tests eliminates false negatives and might comprise a useful procedure for testing mutagenicity in Drosophila.     

Induction of sister chromatid exchanges by chemical mutagens and its possible relevance to DNA repair

Several chemical mutagens were found to induce sister chromatid exchanges in Chinese hamster chromosomes. Among them, effects of 4NQO and MMC were very similar to those of UV light in that the exchange frequency increased with increasing dose of chemicals and that it was markedly lowered in the presence of 1 mM caffeine during a post-treatment period. The frequency of proflavin-induced sister chromatid exchanges was also found to be dose dependent, but it was insensitive to the caffeine post-treatment. On the other hand, no appreciable increase was detected in the incidence of sister chromatid exchanges in MNNG-treated cells over a 100-fold range of variation in chemical dose. Caffeine by itself raised the exchange frequency only slightly over a control level. It was found that 4NQO and MMC exerted remarkable delayed effects on the exchange induction, whereas proflavin did not. This seems to suggest that the lesions caused by the former mutagens would be long-lived and repeatedly provoke sister chromatid exchanges. These data imply that there are several possible ways in which the initial DNA lesions ultimately lead to the formation of sister chromatid exchanges, and that at least UV-, 4NQO- and MMC-induced sister chromatid exchanges would have evolved through a caffeine sensitive repair process, probably related to a post-replication repair of DNA damage.     

The induction of chromosome aberrations in mouse dictyate oocytes by X-rays and chemical mutagens.

Oocytes were collected from female mice and matured in vitro to Metaphase I during the first or third week after treatment with a dose of 400 rad X-rays, 1.6 mg/kg triethylenemelamine (TEM) or 75 mg/kg isopropylmethanesulphonate (IPMS). In week 1 the mean number of oocytes per female was similar for all treatments but in week 3 irradiated females yielded fewer oocytes than the chemically treated or control females. In week 1 the proportion of oocytes maturing was smaller in irradiated females than in the other groups but in week 3 was similar in all groups.Structural chromosome aberrations, scored in the Metaphase I oocytes, were of the chromatid or isochromatid type and involved gaps, breaks, fragments, intrachanges and interchanges. Aberration frequency did not increase with time after either of the chemical mutagens but after irradiation was higher in the third week than in the first week. The aberration yield from IPMS-treated females was similar at both sampling times, while a lower yield was recorded in week 3 following TEM treatment than in week 1.     

Analysis of the types of chromosome aberrations in the combined action of chemical mutagens]

Types of chromosome aberrations were studied in human lymphocyte cultures in combined action of different concentrations of thiophosphamide and dipine in different proportions. The mutagens acted at the Go stage. The range of the concentrations studied was from 3.17-10(-5) M to22.19-10(-5) M. As compared with dipine, the equimolar concentrations of thiophosphamide induced more chromatid exchanges and less sister (isolocus) unions, and also a greater part of single breaks and the part of breaks in the chromatid exchanges of the total number of chromosomal breaks. Both absolute and relative frequencies of chromosome aberrations depended on the mutagens concentration. A change of the thiophosphamide and dipine proportion with a constant total number of molecules of the two mutagens at different concentration levels led to the effect, the level of which was between the effect of action of equimolar concentrations of pure mutagens. This effect depended upon the part of each mutagen in combined treatment. A conclusion was drawn on the additivity of thiophosphamide and dipine action.     

Revision of th distribution of chromosome aberrations induced by chemical mutagens using the BUDR label

Cell distribution was analysed with the help of the BrDU label for the number of chromosome aberrations and breaks induced by one-center (thiophosphamide and phosphamide) and two-center (dipine and fotrine) mutagens at the stage G0 in the Ist mitosis of human lymphocytes harvested at different times of culturing (from 56 to 96 h). The comparison was made between the type of aberration distribution in cells and the dependence of their frequency on the harvesting point for various mutagens. Poisson aberration distribution in cells for two-center mutagens was found to correspond to their constant frequency observed at different times of harvesting. On the other hand, for one-center mutagens, a geometrical distribution of chromosome breaks corresponded to an exponential decrease in their frequency in time. It is suggested that two-center chemical mutagens and ionizing radiation cause largely short-live damages which are realized into chromosome aberrations rather quickly (during one cell cycle). One-center mutagens, however, cause such damages that the probability of their transformation into chromosome aberrations is decreasing rather slowly in time, under the exponential law, and their realization into chromosome aberrations can occur in subsequent cell cycle.     

The correlation between silver-staining and DAPI-induced chromosome undercondensation

The silver-staining pattern of Chinese hamster chromosomes that show DAPI-induced undercondensed areas was studied. The Ag-staining was preceded or not by dehistonizing treatments. In both cases silver preferentially precipitates on undercondensed areas. It is suggested that this phenomenon could be compared to the silver-stainability of the active NORs during mitosis when they remain undercondensed. The possible chemical nature of the protein groups responsible for the silver-staining is discussed.     

Comparison of the levels of chromosome aberration and sister chromatid exchange induced by chemical mutagens in vitro

Dose dependencies of the induction of sister chromatid exchanges (SCEs) and chromosome aberrations were studied under in vivo exposure of mouse bone marrow cells to 5 alkylating agents. The efficacy of the induction of SCEs for all the substances was 20 to 60 times higher than that of the induction of chromosome aberrations. It was demonstrated that SCEs induced by chemical mutagens in vivo and in vitro are more sensitive tests than chromosome aberrations.     

Correlation of the sister chromatid exchange level with chromosome aberrations induced by chemical mutagens in vivo

The data on the dose dependencies of the induction of sister chromatid exchanges (SCE) and chromosomal aberrations during exposure of mouse bone marrow cells in vivo to 5 alkylating substances are provided. The efficacy of SCE induction was found to be higher than that of chromosomal aberrations. It was established that SCE induced by chemical mutagens in vivo and in vitro are more sensitive and stable tests than chromosomal aberrations.     

Specificity of interactions between the individual gene locus and the structure of chemical mutagens

Summary Relative frequencies of visible mutations (egg colour mutants) induced by two similar mutagenic agents of the mustard group, nitromine (methyl-bis--chloroethyl-amine N-oxide) and N. M.-alanine (N-bis--chloroethyl-alanine), have been studied in the silkworm. The solution of either agents was injected into the wild male moths, which were then mated to double recessivepere/pere female moths. (Normal eggs are black,pere/pere andpe/pe eggs are white andre/re eggs, red.) Eggs produced from these matings were examined for their colour and the mutation rates were estimated by the ratio of uncoverings at the marked loci to the total pigmented eggs.Analysis of the results has revealed that the ratio of the mutation rates at thepe-locus to those at there-locus varies markedly according to whether nitromine or N. M.-alanine is injected. When nitromine was used the ratios ofpe-aberrants tore-aberrants were 1.06 and 1.58, while in the case of N. M.-alanine the ratios were 0.59 and 0.60. In many other experiments in which moths were treated with nitromine, thepe/pe ratio was consistently greater than 1 and often as high as 2. The same was true for experiments with irradiated male moths. These results have been discussed in relation to possible specific interactions between chemical mutagens and chromosome loci.     

Mutagenicity of radiations and chemical mutagens in Sorghum

Summary A comparative study on the relative mutagenicity of radiations (X-and gamma rays) and chemical mutagens (EMS, MMS, dES and NEU) in inducing chlorophyll, viable and total mutations was made on three cultivated varieties (Co. 11, Co. 12 and Co. 18) of Eu-Sorghum. A critical comparison of the chlorophyll, viable and total mutations shows that the mutation rate increased with an increase in dose up to a certain dose level beyond which the saturation effect was observed. EMS was found to be the most potent mutagen in inducing chlorophyll, viable and total mutations. The treatments with NEU (viable mutations) and dES (viable and total mutations) also proved to be effective. In a large number of cases the relationship between chlorophyll and total mutations was more close than that of viable to total mutation rates.This work forms part of the thesis submitted for Ph. D. degree of Univ. of Madras.