Incidence of chromosome 8, 10, X and Y aneuploidies in sperm nucleus of infertile men detected by FISH

被引:16
作者
Acar, H [1 ]
Kilinç, M [1 ]
Çora, T [1 ]
Aktan, M [1 ]
Taskapu, H [1 ]
机构
[1] Selcuk Univ, Fac Med, Dept Med Genet, Konya, Turkey
关键词
aneuploidy; infertility; sperm; FISH;
D O I
10.1159/000030531
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
We studied the frequency of aneuploidy in sperm nuclei of six infertile men with abnormal semen profile and normal karyotype, using fluorescence in situ hybridization (FISH) with DNA probes for chromosomes 8, 10, X and Y. The control group consisted of four healthy fertile men with normal karyotype and semen profiles. The purpose of this study was to determine whether there are differences between infertile male donors and control donors for: (1) the incidence of sex chromosome aneuploidy, and (2) the number of disomies for chromosomes 8, and 10 cosegregating with chromosomes X and Y. FISH analysis showed no significant differences of sex ratios of the sperm nuclei in and between infertile and control groups. The most significant abnormalities in the infertile group were clusters of sperm nuclei bearing XY and XYY. In addition, the incidence of disomic sperm nuclei for chromosomes 8 and 10 consegregating with sex chromosomes was not significantly different beween the patient and control groups, nor within them. However, the total frequency of aneuploid sperm nuclei was significantly different beween the infertile group and the control group. We observed a significant excess of sperm nuclei bearing chromosome 10 along with disomy for chromosome Y (10YY). In conclusion, our results from FISH analysis demonstrate a significantly increased frequency of aneuploidy for the sex chromosomes in sperm nuclei from infertile men. Therefore it may be concluded that infertility is a risk factor for sex chromosome aneuploidy in sperm nuclei. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:202 / 208
页数:7
相关论文
共 40 条
[1]   Application of the multi-colour FISH to interphase nuclei and metaphase spreads for simultaneous examination of monosomy 7 and trisomies 8 and 11 in acute myelocytic leukaemia (AML) [J].
Acar, H ;
Acar, A .
CLINICAL AND LABORATORY HAEMATOLOGY, 1997, 19 (01) :33-38
[2]   Detection of trisomy 12 and centromeric alterations in CLL by interphase- and metaphase-FISH [J].
Acar, H ;
Connor, MJ .
CANCER GENETICS AND CYTOGENETICS, 1998, 100 (02) :148-151
[3]   Comparison of gonosomal aneuploidy in spermatozoa of normal fertile men and those with severe male factor detected by in-situ hybridization [J].
Bernardini, L ;
Martini, E ;
Geraedts, JPM ;
Hopman, AHN ;
Lanteri, S ;
Capitanio, GL .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (05) :431-438
[4]   ESTIMATES OF ANEUPLOIDY USING MULTICOLOR FLUORESCENCE IN-SITU HYBRIDIZATION ON HUMAN SPERM [J].
BISCHOFF, FZ ;
NGUYEN, DD ;
BURT, KJ ;
SHAFFER, LG .
CYTOGENETICS AND CELL GENETICS, 1994, 66 (04) :237-243
[5]  
Blanco J, 1996, HUM REPROD, V11, P722
[6]   Increased incidence of hyperhaploid 24,XY spermatozoa detected by three-colour FISH in a 46,XY/47,XXY male [J].
Chevret, E ;
Rousseaux, S ;
Monteil, M ;
Usson, Y ;
Cozzi, J ;
Pelletier, R ;
Sele, B .
HUMAN GENETICS, 1996, 97 (02) :171-175
[7]   Sperm chromosome analysis in the father of a child with a de-novo reciprocal translocation t(11;15)(q12;q22) by G-banding and fluorescence in-situ hybridization [J].
Colls, P ;
Martínez-Pasarell, O ;
Pérez, MM ;
Egozcue, J ;
Templado, C .
HUMAN REPRODUCTION, 1998, 13 (01) :60-64
[8]  
Çora T, 2000, GENET COUNSEL, V11, P25
[9]   MULTIPLE COLORS BY FLUORESCENCE INSITU HYBRIDIZATION USING RATIO-LABELED DNA PROBES CREATE A MOLECULAR KARYOTYPE [J].
DAUWERSE, JG ;
WIEGANT, J ;
RAAP, AK ;
BREUNING, MH ;
VANOMMEN, GJB .
HUMAN MOLECULAR GENETICS, 1992, 1 (08) :593-598
[10]  
Griffin DK, 1996, AM J HUM GENET, V59, P1108