Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
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232 1989 EMS Abstracts<br />
. . . :-- .<br />
NOtE'S immunosuppresive agents . Two to three drops of blood were taken from the ear lobes of<br />
examined persons . TM&,blood was then incubated with 1 .0-2 .0 ml Tris-ammonium chloride<br />
buffer solution 'to'renxTlyze red blood cells . Monolayer cell smears were made with<br />
cytocentrifuge <strong>and</strong> Feulgen stain was applied to detect DNA content . The morphological<br />
observation <strong>and</strong> micronuclei counting were done with light microscope . We found that<br />
the frequencies of micronuclei of lymphocytes in healthy persons were 0 .82 per<br />
thous<strong>and</strong> cells but in patients with esophageal carcinoma were 2 .88 per thous<strong>and</strong> . The<br />
difference of frequencies of micronuclei of lymphocytes between healthy persons <strong>and</strong><br />
patients with esophageal carcinoma was statastically significant (PA0 .001) . The<br />
method we used to detect micronuclei of lymphocytes was fast <strong>and</strong> reliable <strong>and</strong> easily<br />
accepted by patients examined .<br />
http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />
674<br />
4IT' STU7Y i :+CCU' ; L :^_ IO° OF 2.L' :1 .. . . : IN Gr'.Rh: CSLLS ON INDUCTIi . :i<br />
OF ~.lDICG-_? ;~TC7.L^.OLCGICAL 3F :^r:CT .<br />
Zhu Bhoup n~, heov Siyinq, -ad lP-n :^- Liuyi, Suzhou Nedical College, Suzhou(China)<br />
T~j purpose of the present study is to ascertain r,omp,?~rative retontion of 147Pn<br />
o„- Cs in qerm cells on induction of chromnsome aberraM ns of sparmatogonium <strong>and</strong><br />
eb :iormall+.i .e in sperm . Results it .dicated that after iv Pm throu,h 50 d observstion<br />
. The rEtr.nt~oPC~~a~s in tastis were well describad by an exponential expression<br />
13~(t)=0 .1872xe- , where the retention ^=1C5 ( : . 'lhlle th3 .fat~~ntion data of<br />
Cs in t•?stiF w•er^ described by e-n expreswlofi : =tlt).O,OC15za , where the<br />
retention T, was on}X75 .2 d, 3xperimsnts indicated that the retention value aQJ4thc<br />
abs.irption ose of Pn i?A°a is ree sirnificantly high in comparism with C s .<br />
Internal conta.nins!ion of ?~ or Ce can be induced chromosome aberrations in<br />
germ cells <strong>and</strong> abnormalltiT17in spaj~b Atnona the type of chromosome aberrations of<br />
apermato-onium induc,~d bv _m or Ce includin- ^a~, chromatid breakage, chromosome<br />
brea ::age, <strong>and</strong> tranalocation, as woll as poly :'-oid spermatogonium . },oreover,<br />
the chromosoma aberrft3on rctt*s <strong>and</strong> pol,T,:loid cells were elevated when the periods<br />
of conta^:ination of Pm :rora prolon,? !d . ,1t th : semt_ t#" ehromoso:ae fragment <strong>and</strong><br />
If~nalocations of primary spermatocyte also induced by Pm . By compaTign with<br />
:m, ho-ver, the induction of cytogenetic effects on germ cells by a wke<br />
quite low.<br />
675<br />
INDUC'TION OF MUTATION IN F-'aihcrichin cofi BY DIMETHYISULFATE IS INFLUENCED BY SOS :<br />
OBSERVA'11ONS OF THE MUTATIONAL SPF.C IFICI'IY OF DMS AND E7HYL ETHANESULFONATE<br />
IN WILD-TYPE AND UmuC STRAINS . Maria Zieknaka, Janet Smylie, Jiso Iian Li <strong>and</strong> Barry W . Olickman .<br />
Dept . of Biology. York llniversity, Toronto Canada M3J 1P3 .<br />
In this study we have undertaken to examine how mutagenesis resulting from EMS <strong>and</strong> DMS is<br />
influenced by the error-prone misrepair pathway of E. rofi . We Investigated the mutational specificity of<br />
these alkylating agents by DNA sequencing <strong>and</strong> oligonucleotide probing methodologies In the first 180<br />
base pairs of the Inrl gene of F. rnfi in wild-type <strong>and</strong> UmuC strains . Consistent with the established<br />
alkylating ability of these agents, the O :C _> A :T transition dominated the resulting spedra . EMS<br />
elicited an identical mutagenic response in the two strairo ; after treatment with 3mM KMS there was a<br />
15-fold increase in mutation frequency at 57% survivaL Mutational specificity of EMS in the l1muC<br />
background was identical to that found in the wild-type strain ; O:C - > A :T transitions accounted for<br />
over 96% of the mutational events in each spectrum <strong>and</strong> their distribution was identical . DMS<br />
mutagenicity decreased in the UmuC background from a 128-fold increase in mutation frequency at 14%<br />
survival (wild-typel to a 26-fokl increase at 6O/o sunival. The influence of UmuC function was also<br />
apparent at the DNA sequence level . In the wild-type background t3 :C - > A:T transitions accounted for<br />
74% of the mutations, which were alan characterised by a significant contribution of additional<br />
mutatiomd events including Ai r=- (hC' trnnsitkms, all classes of transverskms <strong>and</strong> framoshifu . In<br />
eontrast, after DMS treatntent in a UmuC strain 82% of all mutational events were (t :C .• > A:T<br />
transitions with a different site specificity from that recovered in the wild-type background. The other<br />
claases of events found consisted of A :T => T :A <strong>and</strong> C; :C - > T:A tramversions, frameshUts <strong>and</strong> a<br />
duplication. We conclude that mutagenesis by EMS Is independent of the UmuC function in contrast to<br />
mutagenesis by 1)MS which shrn.s a marked Umu inhtence .<br />
676<br />
DETERMINATION OF SPONTANEOUS AND ENU-INDUCED MUTANT FREQUENCIES IN<br />
CYNOMOLOGOUS MONKEYS . D .M .Zimmer, C .S.Aaron, R .J .Albertini, <strong>and</strong> J .P.O'NeiII. The<br />
Upjohn Co. <strong>and</strong> University of Vermont, USA .<br />
We have undertaken a study of mutagenesis In primates (cynomologous monkeys) to<br />
determine whether such an assay offers better means of risk assessment than currently<br />
used in vitro <strong>and</strong> rodent tests. Using methods similar to those described by Albertini<br />
(Mutat . Res. 150 (1985), 411-422J, mutation at the HPRT locus was monitored by<br />
determining the ability of PHA stimulated peripheral T- lymphocytes to form clones In the<br />
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