MITOTIC INDIRECT NONDISJUNCTION IN PHYTOHEMAGGLUTININ-STIMULATED HUMAN-LYMPHOCYTES

被引:17
作者
GUSTAVINO, B
DEGRASSI, F
FILIPPONI, R
MODESTI, D
TANZARELLA, C
RIZZONI, M
机构
[1] UNIV ROMA TORVERGATA,DIPARTIMENTO BIOL,I-00173 ROME,ITALY
[2] UNIV ROMA LA SAPIENZA,CNR,CTR GENET EVOLUZIONIST,ROME,ITALY
[3] UNIV ROMA LA SAPIENZA,DIPARTIMENTO GENET & BIOL MOLEC C DARWIN,ROME,ITALY
[4] UNIV LAQUILA,DIPARTIMENTO BIOL,CATTADRA PATOL CLIN,LAQUILA,ITALY
[5] UNIV ROMA 3,DIPARTIMENTO BIOL,ROME,ITALY
关键词
D O I
10.1093/mutage/9.1.17
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In a previous publication we demonstrated that in cells of Vicia faba micronuclei derived from whole lagging chromosomes or chromatids may perform DNA synthesis and mitotic condensation in synchrony with main nuclei and be regained by main nuclei at the next mitosis, giving rise to trisomic cells together with diploids. This process was called 'mitotic indirect non-disjunction' (MIND). In the present work the occurrence of MIND was studied in human lymphocytes cultivated in vitro. Human lymphocytes were treated with low colcemid concentrations until fixation; BrUdR was supplied together with colcemid to distinguish the number of mitoses performed by the cells (M(1), M(2) and M(3) cells). The frequencies of M(1) ana-telophases,vith single lagging chromosomes/chromatids and of M(2)(+) prophases with single micronuclei in synchronous motitic condensation with main nuclei were evaluated. On this basis the expected frequencies of both monosomic and trisomic M(2) cells were calculated, according to the hypothesis of MIND. Their observed frequencies were very close to those expected. These results support the hypothesis of the occurrence of MIND in human lymphocytes.
引用
收藏
页码:17 / 21
页数:5
相关论文
共 18 条
[1]   NON-RANDOM CHROMOSOME LOSS IN PHA-STIMULATED LYMPHOCYTES FROM NORMAL INDIVIDUALS [J].
BROWN, T ;
FOX, DP ;
ROBERTSON, FW ;
BULLOCK, I .
MUTATION RESEARCH, 1983, 122 (3-4) :403-406
[2]   IDENTIFICATION OF ANEUPLOIDY-INDUCING AGENTS USING CYTOKINESIS-BLOCKED HUMAN-LYMPHOCYTES AND AN ANTIKINETOCHORE ANTIBODY [J].
EASTMOND, DA ;
TUCKER, JD .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1989, 13 (01) :34-43
[3]   KINETOCHORE DETECTION IN MICRONUCLEI - AN ALTERNATIVE METHOD FOR MEASURING CHROMOSOME LOSS [J].
FENECH, M ;
MORLEY, AA .
MUTAGENESIS, 1989, 4 (02) :98-104
[4]   SPINDLE MICROTUBULAR DYSFUNCTION IN MOTHERS OF DOWN SYNDROME CHILDREN [J].
FORD, JH .
HUMAN GENETICS, 1984, 68 (04) :295-298
[5]  
FORD JH, 1988, AM J HUM GENET, V43, P733
[6]   DISPLACEMENT OF CHROMOSOMES IN MITOSIS - A TECHNIQUE FOR ASSESSING DIFFERENTIAL CHROMOSOME ERROR [J].
FORD, JH ;
ROBERTS, C .
CYTOGENETICS AND CELL GENETICS, 1983, 36 (03) :537-541
[7]  
FORD JH, 1985, ANEUPLOIDY ETIOLOGY, P291
[8]   A COMPARISON BETWEEN SHORT-TERM EVOLUTION OF MICRONUCLEI INDUCED BY X-RAYS AND COLCHICINE IN ROOT-TIPS OF VICIA-FABA [J].
GUSTAVINO, B ;
VITAGLIANO, E ;
SOTTILI, A ;
RIZZONI, M .
MUTATION RESEARCH, 1987, 192 (02) :109-119
[9]   CHROMOSOME PREPARATIONS OF LEUKOCYTES CULTURED FROM HUMAN PERIPHERAL BLOOD [J].
MOORHEAD, PS ;
NOWELL, PC ;
MELLMAN, WJ ;
BATTIPS, DM ;
HUNGERFORD, DA .
EXPERIMENTAL CELL RESEARCH, 1960, 20 (03) :613-616
[10]   HUMAN LEUKOCYTE TEST SYSTEM .7. FURTHER INVESTIGATIONS CONCERNING MICRONUCLEUS-DERIVED PREMATURE CHROMOSOME CONDENSATION [J].
OBE, G ;
BEEK, B .
HUMANGENETIK, 1975, 30 (02) :143-154