Extruded micronuclei induced by colchicine or acrylamide contain mostly lagging chromosomes identified in paintbrush smears by minor and major mouse DNA probes

被引:27
作者
SchrieverSchwemmer, G
Kliesch, U
Adler, ID
机构
[1] GSF FORSCHUNGSZENTRUM UMWELT & GESUNDHEIT GMBH,INST SAUGETIERGENET,D-85764 NEUHERBERG,GERMANY
[2] UNIV MUNICH,TIERARZTLICHE FAK,LEHRSTUHL ALLGEMEINE PATHOL & NEUROPATHOL,D-80539 MUNICH,GERMANY
关键词
D O I
10.1093/mutage/12.4.201
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In the mouse bone marrow micronucleus assay, it was studied whether micronuclei (MN) could be expelled from polychromatic erythrocytes (PCE) in a similar way to the main nucleus, To avoid the disrupting centrifugation step of the conventional bone marrow preparation procedure, the paintbrush technique was used in the present experiments. With May-Grunwald-Giemsa staining of paintbrush slides, 5% of the colchicine (COL)-induced MN were found attached to the outside membranes of PCE and were regarded as extruded, Of the acrylamide (AA)-induced MN, 22% were extruded, After fluorescence in situ hybridization (FISH) of a total of 300 MN per chemical treatment with the mouse minor and major satellite DNA probes, 9.7% MN were extruded in the COL group and 8.3% MN were extruded in the AA group, FISH showed that 76% of the retained COL-induced MN were signal-positive, indicating that they contained entire chromosomes, With AA, 29% minor-positive and 28.3% major-positive retained MN were found, confirming its known clastogenicity, However, the observed frequency of signal-positive MN (1.7 MNPCEpos/1000 PCE) in the AA group was about three times higher than in the control (0.5 MNPCEpos/1000 PCE) which indicates that AA has aneugenic potential, FISH analysis of the extruded MN showed 72-100% major as well as minor signals, It is concluded that expelled MN contain mostly entire chromosomes.
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页码:201 / 207
页数:7
相关论文
共 39 条
[1]  
Adler I.-D., 1984, MUTAGENICITY TESTING, P275
[2]   CLASTOGENIC EFFECTS OF ACRYLAMIDE IN MOUSE BONE-MARROW CELLS [J].
ADLER, ID ;
INGWERSEN, I ;
KLIESCH, U ;
ELTARRAS, A .
MUTATION RESEARCH, 1988, 206 (03) :379-385
[3]   PERTURBATION OF CELL-DIVISION BY ACRYLAMIDE INVITRO AND INVIVO [J].
ADLER, ID ;
ZOUH, R ;
SCHMID, E .
MUTATION RESEARCH, 1993, 301 (04) :249-254
[4]   DOSE-RESPONSE FOR HERITABLE TRANSLOCATIONS INDUCED BY ACRYLAMIDE IN SPERMATIDS OF MICE [J].
ADLER, ID ;
REITMEIR, P ;
SCHMOLLER, R ;
SCHRIEVERSCHWEMMER, G .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1994, 309 (02) :285-291
[5]   MOUSE MICRONUCLEUS TESTS WITH KNOWN AND SUSPECT SPINDLE POISONS - RESULTS FROM 2 LABORATORIES [J].
ADLER, ID ;
KLIESCH, U ;
VANHUMMELEN, P ;
KIRSCHVOLDERS, M .
MUTAGENESIS, 1991, 6 (01) :47-53
[6]   RELATIONSHIP OF MOUSE MINOR SATELLITE DNA TO CENTROMERE ACTIVITY [J].
BROCCOLI, D ;
MILLER, OJ ;
MILLER, DA .
CYTOGENETICS AND CELL GENETICS, 1990, 54 (3-4) :182-186
[7]   DETECTION OF HYDROQUINONE-INDUCED NONRANDOM BREAKAGE IN THE CENTROMERIC HETEROCHROMATIN OF MOUSE BONE-MARROW CELLS USING MULTICOLOR FLUORESCENCE IN-SITU HYBRIDIZATION WITH THE MOUSE MAJOR AND MINOR SATELLITE PROBES [J].
CHEN, HW ;
TOMAR, R ;
EASTMOND, DA .
MUTAGENESIS, 1994, 9 (06) :563-569
[8]  
EASTMOND DA, 1993, NATO ASI SER, V72, P377
[9]   REEVALUATION OF THE INDUCTION OF SPECIFIC-LOCUS MUTATIONS IN SPERMATOGONIA OF THE MOUSE BY ACRYLAMIDE [J].
EHLING, UH ;
NEUHAUSERKLAUS, A .
MUTATION RESEARCH, 1992, 283 (03) :185-191
[10]   THE USE OF FLUORESCENCE IN-SITU HYBRIDIZATION FOR THE DETECTION OF ANEUGENS IN CYTOKINESIS-BLOCKED MOUSE SPLENOCYTES [J].
FAROOQI, Z ;
DARROUDI, F ;
NATARAJAN, AT .
MUTAGENESIS, 1993, 8 (04) :329-334