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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)

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