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t<br />

SCe <strong>and</strong> serum cotinine were determined for 17 smokers . SCE for each person<br />

was determined by analyong 100 second-division lymphocytes from whole blood<br />

cultures . SCE per persoiC ranged from 4 .54 to 10 .16 exchanges per coll .<br />

Cotinine values were determined in duplicate for blood drawn at the same<br />

time . These values were between 13 <strong>and</strong> 500 ng/ml . In this study, we found a<br />

positive correlation (R .0 .53, p- 0 .03) between SCE <strong>and</strong> serum cotinine . Larger<br />

studies are needed to confirm this finding .<br />

473<br />

4Hk: lNTEGENICITY STUDY OF 69'NINGOCOCCAI: I'OLYSACCIIARIED-TETANUS TOXOIL CONJUGATE<br />

Ren Neiyue, Zhao Hong, tang Yaozhone, <strong>and</strong> Li genqing, Shanghai Institute of Biological<br />

Products, Shanghai, China<br />

Mer.ingococcal group A'polyaaccharide-tetanus toxoid conjugate was combined with po-<br />

lysaccharide <strong>and</strong> protein so as to increase the immunogenicity of both the polysaccheride<br />

<strong>and</strong> tetanus toxoid in the guinea-pigs <strong>and</strong> mice . It In hopeful that the conjugate<br />

will be used widely in human beings, eapecielly in very young children In Chine . Here<br />

we examined the mutagenicity of the conjugate for Ames assay, micronucleus test <strong>and</strong><br />

chromosome aberration analysis in Chinese Han .ater Lung cells . The result indicated th-<br />

at the conjugate could not increase remarkarly either the revertants of four test strains<br />

( TA97, TA98 . TA100, <strong>and</strong> TA102 ) with of without 89 mix In Ames asaay at the con-<br />

centration range of 0 .2-125 ug/plate, or the rate of micronucleus after treatment for<br />

2t hours in the polyghromatic erthrocytes of tho bone mRrrow cells in mice at the con-<br />

centration range of 48-1200 ug/I(g body weight . The result also indicated that half of<br />

the cells was inhirited In vitro when the roriugete was et the concentration if 0 .92<br />

ug/ml <strong>and</strong> the conjugate could not increase remarkably the rate of chromosome aberrati-<br />

on after treFtmertt for u hours with S9 mix or for 24 or 48 hours without 59 mix at the<br />

concentration range of 0 .25-1 .0iug/ml in chromosorre aberration anelysis . It wss belie-<br />

ved that the conjugate hae no mutegenicity in our leb. f<br />

474 •<br />

THE LACK OF DNA HOMOLOGY IN PAIRS OF DNA DIVERGENT CHROMOSOMES SENSITIZES THEN TO<br />

LOSS BY DNA DAMAGE . M .A . Resnick <strong>and</strong> T .Nilsson-Tillgren . Yeast Genetics Group,<br />

National Inst . Environmen-EaT~eafth Sciences, Research Triangle Park, NC, USA ;<br />

Inst . of Genetics, U . Copenhagen, Denmark<br />

Chromosomal DNA is considered a priori to be a target for production of numerical<br />

(whole chromosome) aneuploidy <strong>and</strong> DNA repair would be expected to play a role .<br />

Using the yeast Saccharom ces cerevisiae, we have addressed the importance of<br />

recombinational repa r requ re or ouble-str<strong>and</strong> break [DSB] repair) in the<br />

maintenance of complete chromosomes . Specifically, aneuploidy induction by Ionizing<br />

radiation has been examined in diploids which had either one chromosome III<br />

or chromosome V replaced by a DNA divergent (homoeologous) chromosome from S .<br />

carlsber ensis . While they are functionally equivalent, the lack of precise DNA<br />

omo oof chromosome III or all of V was expected to prevent recombinational<br />

repair . The absence of recombinational repair (presumably of DSBs) in the<br />

divergent chromosomes results in aneuploidy levels of 5 to 15% at nonlethal doses<br />

<strong>and</strong> a low level of rearrangements . The induction appears to level off suggesting<br />

alternative ways of dealing with double-str<strong>and</strong> breaks . For homologous chromosomes,<br />

the aneuploidy frequency is 20 to 50 X lower . Based on genetic <strong>and</strong> physical analyses,<br />

the aneuploidy is due to chromosome loss, not chromosome deletions nor<br />

malsegregation . Thus, the absence of opportunity for homologous recombinational<br />

repair of double-str<strong>and</strong> damage results in chromosome loss . We suggest that nonhomologous<br />

regions of otherwise homologous chromosomes may be important targets for<br />

the induction of aneuploidy . The relevance of these observations to those in mammalian<br />

cells will be discussed .<br />

475<br />

BIOMOHITORIPG OF INDIVIDUALS OCCUPATIONALLY EIpOSED TO AROMATIC A11IwES .<br />

L .R .Ribeiro,D .M .F .Salvadori,E .M .M .Cerqueira,H .S .Barbosa,M .D .M .Oliveira <strong>and</strong> A .R .Silva .<br />

Universidade Federal da Bahia, Salvador, BA (BRASIL) .<br />

Several reports show high frequency of genetic damage <strong>and</strong> high incidence of urinary<br />

bladder cancer due to the presence of mutagenic <strong>and</strong> carcinogenic products in the urinary<br />

tract,apecially the aromatic amines .The genetic <strong>and</strong> carcinogenic risks of workers occupationally<br />

exposed to aromatic amines <strong>and</strong> the presumed antimutagenic <strong>and</strong> anticarcinogenic<br />

potential of provitamin a-carotene are being studied at the production plant at<br />

the Petrochemical Industrial Complex of CamaSari,BA,Brazi1 .30 male individuals exposed<br />

http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />

1989 EMS Abstracts 163<br />

Notes

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