Meiotic segregation analysis in a t(4;8) carrier: comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei

被引:39
作者
Oliver-Bonet, M [1 ]
Navarro, J
Codina-Pascual, M
Carrera, M
Egozcue, J
Benet, J
机构
[1] Univ Autonoma Barcelona, Unitat Biol, Fac Med, Dept Biol Cellular Fisiol & Immunol, E-08193 Barcelona, Spain
[2] Ctr Patol Celular, Barcelona, Spain
[3] Autonomous Univ Barcelona, Unitat Biol Cellular, Fac Ciencies, Dept Biol Cellular Fisiol & Immunol, E-08193 Barcelona, Spain
关键词
sperm chromosome; sperm nuclei; meiotic segregation; chromosome rearrangements; aneuploidy; FISH;
D O I
10.1038/sj.ejhg.5200654
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Meiotic segregation of a t(4;8)(q28;p23) translocation carrier was determined by two different methods to compare the final results. A total of 352 sperm chromosome complements, obtained after human-hamster in vitro fertilisation, were analysed by whole chromosome painting, and 6590 sperm heads were studied by fluorescence in situ hybridisation (FISH). Frequencies of alternate, adjacent I, adjacent II and 3:1 segregations were, for sperm chromosomes, 35.5, 33.2, 19.9 and 11.3% respectively. For sperm head analysis, results were 30.5, 28.5, 20.5 and 19.5% respectively. There were no statistically significant differences between the two methods with respect to the observed frequencies of sperm with balanced and unbalanced chromosome constitutions. Among unbalanced gametes, the methods differed only in the frequency of 3:1 segregation (chi (2), P <0.0001). Different factors that could explain this result are discussed. To determine possible interchromosomal effects, multicolour FISH was used on sperm heads. Disomy rates of sex and 18 chromosomes were higher in the translocation carrier than in the control. The differences observed were statistically significant (P <0.0001 for chromosomes X and 18, and P=0.0091 for chromosome Y).
引用
收藏
页码:395 / 403
页数:9
相关论文
共 43 条
[21]   Analysis of structural and numerical chromosome abnormalities in sperm of normal men and carriers of constitutional chromosome aberrations. A review [J].
Guttenbach, M ;
Engel, W ;
Schmid, M .
HUMAN GENETICS, 1997, 100 (01) :1-21
[22]   Analysis of segregation and aneuploidy in two reciprocal translocation carriers, t(3;9)(q26.2;q32) and t(3;9)(p25;q32), by triple-color fluorescence in situ hybridization [J].
Honda, H ;
Miharu, N ;
Ohashi, Y ;
Honda, N ;
Hara, T ;
Ohama, K .
HUMAN GENETICS, 1999, 105 (05) :428-436
[23]  
HULTEN M, 1974, HEREDITAS, V76, P55
[24]  
JACOBS PA, 1981, AM J HUM GENET, V33, P44
[25]   RECIPROCAL TRANSLOCATIONS - A WAY TO PREDICT THE MODE OF IMBALANCED SEGREGATION BY PACHYTENE-DIAGRAM DRAWING - A STUDY OF 151 HUMAN TRANSLOCATIONS [J].
JALBERT, P ;
SELE, B ;
JALBERT, H .
HUMAN GENETICS, 1980, 55 (02) :209-222
[26]   FURTHER-STUDIES ON BIVALENT CHIASMA FREQUENCY IN HUMAN MALES WITH NORMAL KARYOTYPES [J].
LAURIE, DA ;
HULTEN, MA .
ANNALS OF HUMAN GENETICS, 1985, 49 (JUL) :189-201
[27]  
LEJEUNE J, 1963, PEDIATRICS, V32, P326
[28]  
MARTIN RH, 1984, CLIN GENET, V25, P357
[29]   Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH [J].
Martini, E ;
von Bergh, ARM ;
Coonen, E ;
de Die-Smulders, CEM ;
Hopman, AHN ;
Ramaekers, FCS ;
Geraedts, JPM .
HUMAN GENETICS, 1998, 102 (02) :157-165
[30]   Molecular analysis of the chromosomal equipment in spermatozoa of a 46, XY, t (7;8) (q11.21;cen) carrier by using fluorescence in situ hybridization [J].
Mercier, S ;
Morel, F ;
Fellman, F ;
Roux, C ;
Bresson, JL .
HUMAN GENETICS, 1998, 102 (04) :446-451