Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
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'ne oencentromer c region of the Tchromosome : 011123. complementarv to a DNA sequence repeated 50 times in thee<br />
penrentromenc region of chromosome 9 : pNlt}it, honwiogous to the N-Myc oncogene <strong>and</strong> specific for chromosome 1 in the<br />
Neuroblastoma cell line LAN-1, wheWthe oncogene is amplified 50 times . /e situ hybridization experiments have been<br />
cerrred out on human lymphocytes with Y97 <strong>and</strong> Op23 <strong>and</strong> on Neuroblastoma cell hnes with oNb19-21 . Preliminary<br />
exper ments, performed on untreated cultures, to test the efficiency of the probes . showed an exceedingly high proportion of<br />
hvpodiplo,d nuclei due to technical artifacts . Therefore hyperdiploiov has been taken as a reliable index of induced sneuploidv .<br />
In order to check the validity of the assay we analyzed four known aneuploidy inducers, iumely fknomyl (8E), 6rieeofulvln<br />
!nF 1 . Chloral hydrate (CH), Diethvlstiibestroi (DES) <strong>and</strong> a putative carcinogenic agent NitrilTnacebcAcid INTAI . A significant<br />
increase in the percentage of hyperdiploid nuclei has been found with 8E . 6F, CH <strong>and</strong> DES ; a dose-related effect has been<br />
revealed w,ti` CH <strong>and</strong> DES . NTA did not show any effect in the induction of aneuplmdv . To improve the efficiency of the method<br />
we have compared the conventional aRO'f ddiographlc proCeDUre with that based on immunofluorescence . To this purpose<br />
parallel experiments heve been carried out with radioactive <strong>and</strong> biotmvlated probes using DES as a test compound . The nonrIclioaCtlve<br />
technique turned Out to be more sensitive <strong>and</strong> therefore more suitable for screening new compounds . The positive<br />
response obtained with agents that induce chromosome number variation by different mechanisms of action indicates that the<br />
rriethod we have devroloped may be of general application for testing aneuploidy Inducers is riua Moreover, the possibility of<br />
scoring large cell samples makes interphase analysis suitable for tne cytogenetic monitoring of exposed populations .<br />
595<br />
APPRAISAL OF GENOTOXIC EFFECTS OF AGROCHEMICALS IN HIGHER PLANTS USING IN VIVO AND<br />
IN VITRO END POINTS .<br />
K .Vaidyanath <strong>and</strong> T .Suryakumari, Department of Genetics, Osmania University,<br />
Hyderabad - 500 007 (A .P .) India .<br />
The use of different agrochemicals to control diseases, pests <strong>and</strong> weeds is<br />
an essential component of the modern agricultural technology . Though economic advantages<br />
of such practice is appreciated, it is belived that exposure to agrochemicals<br />
has many genetic consequences . To have a realistic appraisal of genotoxicity, three<br />
commonly used Chemicals viz ., Ethylene dibromide, Phenyl mercury acetate <strong>and</strong> Ekalux,<br />
have been studied using multiple end points like, somatic chromosomal aberrations,<br />
heritable germinal mutations at specific <strong>and</strong> non-specific locus, <strong>and</strong> in vitro growth<br />
of callus cultures . Significant frequency of chromosomal aberrations, -c-h1orophyll<br />
deficient seedlings in M. generation, specific locus mutations at waxy locus<br />
(Wx - wx), pollen sterility, polygenic variability in H3 generation <strong>and</strong> iphibition<br />
of callus growth have been observed . The overall results of the study suggests that<br />
any one or combination of genetic end points could be employed for the effective<br />
screening of environmental mutagens .<br />
596<br />
ACRYLAMIDE-1NDUCED CHROMOSONE-T1iPE ABBRRAT'IONS IN SPERMiOGENIC STAGES EVALUATED<br />
IN THE FIRST CLEAVAGE ME'1'AYHASES IN '1'Hh MOUSI : . N .Y . Vald>lvia, N .M . Lafuente <strong>and</strong><br />
M . Katoh, Fac . Odontoloqia, U . de Chile, bTGO (CHILIi) <strong>and</strong> Hatano Research Instztute,<br />
F .D .S .C ., Kanagawa (JAPAN) .<br />
Because of the evidences reported by Seqa, et al . (19`" Annual Meeting BMS) that acr7laaide (AA)<br />
binding to protasine of speraioqenic stages in the souse appears to be correlated with the pattern<br />
of genetic dasage oroduced by this cneaical in late speraatids <strong>and</strong> early speraatoza stages (Shelby,<br />
et a1 ., 1986) cytogenatic evaluation of these sase sensitive stages was perforaed in sarlir cleavage<br />
of souse eabryos . Adult sale M sice were intraperitoneally (i .p.) injected with 150 sq AA/kq <strong>and</strong><br />
aated to untreated fesales at intervals ranging fros 6 to 9 <strong>and</strong> 10 to 13 days after tratsent . The<br />
plugged fesales sere i .p . injected with colchicine <strong>and</strong> the fert:lized ova were collected to the first<br />
cleavage aitosis, at sich tiae the male chroaosou cosplesent su analyzed for strsctaral ohrosososal<br />
da.age . The chroaosose-t)