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
[1]   Screening for abnormalities of chromosomes X, Y, and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program [J].
Aran, B ;
Blanco, J ;
Vidal, F ;
Vendrell, JM ;
Egozcue, S ;
Barri, PN ;
Egozcue, J ;
Veiga, A .
FERTILITY AND STERILITY, 1999, 72 (04) :696-701
[2]  
ASHLEY T, 1988, GENETICS, V118, P307
[3]   CHROMOSOME SEGREGATION INTO THE SPERMATOZOA OF 2 MEN HETEROZYGOUS FOR DIFFERENT RECIPROCAL TRANSLOCATIONS [J].
BALKAN, W ;
MARTIN, RH .
HUMAN GENETICS, 1983, 63 (04) :345-348
[4]   CHROMOSOME-ABNORMALITIES IN HUMAN SPERMATOZOA AFTER ALBUMIN OR TEST-YOLK CAPACITATION [J].
BENET, J ;
NAVARRO, J ;
GENESCA, A ;
EGOZCUE, J ;
TEMPLADO, C .
HUMAN REPRODUCTION, 1991, 6 (03) :369-375
[5]  
Blanco J, 1996, HUM REPROD, V11, P722
[6]   Interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei [J].
Blanco, J ;
Egozcue, J ;
Vidal, F .
HUMAN GENETICS, 2000, 106 (05) :500-505
[7]   FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t(5;8)(q33;q13) [J].
Blanco, J ;
Egozcue, J ;
Clusellas, N ;
Vidal, F .
CYTOGENETICS AND CELL GENETICS, 1998, 83 (3-4) :275-280
[8]  
BRAMBATI B, 1990, ESTABLISHING SUCCESS, V66, P269
[9]  
BRANDRIFF B, 1986, AM J HUM GENET, V38, P197
[10]  
BURNS JP, 1986, AM J HUM GENET, V38, P954