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Erschienen in: Journal of Assisted Reproduction and Genetics 7/2011

01.07.2011 | Genetics

Chromosomal segregation in spermatozoa of five Robertsonian translocation carriers t(13;14)

verfasst von: Manel Mahjoub, Meriem Mehdi, Sonia Brahem, Hatem Elghezal, Samira Ibala, Ali Saad

Erschienen in: Journal of Assisted Reproduction and Genetics | Ausgabe 7/2011

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Abstract

Purpose

To analyse the segregation of a Robertsonian translocation t(13;14) in five male carriers, and to verify a possible inter-chromosomal effect (ICE) of the Robertsonian translocation on chromosomes 18, X, and Y.

Methods

The spermatozoa of these patients (n = 5) and of 15 donors with normal semen parameters and 46,XY karyotype were analysed using triple colour FISH with locus specific probes for chromosomes 13, 14, and 21 and by triple colour FISH for chromosomes X, Y, and 18.

Results

The frequency of balanced spermatozoa resulting from alternate segregation varied between 62.16% and 81.70% with a mean of 71.5%. The rates of unbalanced spermatozoa resulting from adjacent segregation varied between 13.4% and 25.1% with a mean of 18.26%. Triple colour FISH X-Y-18 showed a significant increase in disomy frequencies of these chromosomes in comparison with controls, indicating an ICE.

Conclusion

In spite of the high number of normal/balanced frequencies, there remain many unbalanced spermatozoa resulting from adjacent mode of segregation. This raises the question of the unbalanced chromosomal risk for the offspring of 45,XY, t(13;14) males and the importance of the genetic counselling prior to ICSI or IVF treatment for couples where the male is a Robertsonian translocation carrier.
Literatur
1.
Zurück zum Zitat Nielsen J, Wohlert M. Chromosome abnormalities found among 34910 newborn children: results from 13 –year incidence study in Arhus, Denmark. Hum Genet. 1991;87:81–3.PubMedCrossRef Nielsen J, Wohlert M. Chromosome abnormalities found among 34910 newborn children: results from 13 –year incidence study in Arhus, Denmark. Hum Genet. 1991;87:81–3.PubMedCrossRef
2.
Zurück zum Zitat Vidal F, Templado C, Navarro J, Marina S, Egoscue J. Meiotic and synaptonemal complexes studies in a 14/21 translocation carrier. Int J Androl. 1982;5:21–6.PubMedCrossRef Vidal F, Templado C, Navarro J, Marina S, Egoscue J. Meiotic and synaptonemal complexes studies in a 14/21 translocation carrier. Int J Androl. 1982;5:21–6.PubMedCrossRef
3.
Zurück zum Zitat Sybenga J. Chromosome structural variants. In: Sybenga J, editor. General cytogenetics. Amsterdam: North-Holland; 1975. p. 165–212. Sybenga J. Chromosome structural variants. In: Sybenga J, editor. General cytogenetics. Amsterdam: North-Holland; 1975. p. 165–212.
4.
Zurück zum Zitat Egoscue S, Blanco J, Vendrell JM, Garcia F, Veiga A, Aran B, et al. Human male infertility: chromosome anomalies, meiotic desorders, abnormal spermatozoa and recurrent abortion. Hum Reprod Update. 2000;6:93–105.CrossRef Egoscue S, Blanco J, Vendrell JM, Garcia F, Veiga A, Aran B, et al. Human male infertility: chromosome anomalies, meiotic desorders, abnormal spermatozoa and recurrent abortion. Hum Reprod Update. 2000;6:93–105.CrossRef
5.
Zurück zum Zitat Balkan W, Martin RH. Segregation of chromosomes into the spermatozoa of a man heterozygeous for a 14;21 Robertsonian translocation. Am J Med Genet. 1983;16:169–72.PubMedCrossRef Balkan W, Martin RH. Segregation of chromosomes into the spermatozoa of a man heterozygeous for a 14;21 Robertsonian translocation. Am J Med Genet. 1983;16:169–72.PubMedCrossRef
6.
Zurück zum Zitat Rousseaux S, Hazzouri M, Pelletier R, Monteil M, Usson Y, Sèle B. Disomy rates for chromosomes 14 and 21 studied by fluorescent in-situ hybridization in spermatozoa from three men over 60 years of age. Mol Hum Reprod. 1998;4:695–9.PubMedCrossRef Rousseaux S, Hazzouri M, Pelletier R, Monteil M, Usson Y, Sèle B. Disomy rates for chromosomes 14 and 21 studied by fluorescent in-situ hybridization in spermatozoa from three men over 60 years of age. Mol Hum Reprod. 1998;4:695–9.PubMedCrossRef
7.
Zurück zum Zitat Honda H, Miharu N, Ohashi Y, Honda N, Hara T, Ohama K. 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. Hum Genet. 1999;105:428–36.PubMedCrossRef Honda H, Miharu N, Ohashi Y, Honda N, Hara T, Ohama K. 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. Hum Genet. 1999;105:428–36.PubMedCrossRef
8.
Zurück zum Zitat Honda H, Miharu N, Samura O, He H, Ohama K. Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization. Hum Genet. 2000;106:188–93.PubMedCrossRef Honda H, Miharu N, Samura O, He H, Ohama K. Meiotic segregation analysis of a 14;21 Robertsonian translocation carrier by fluorescence in situ hybridization. Hum Genet. 2000;106:188–93.PubMedCrossRef
9.
Zurück zum Zitat Frydman N, Romana S, Le Lorc’h M, Vekemans M, Frydman R, Tachjian G. Assisting reproduction of infertile men carrying a Robertsonian translocation. Hum Reprod. 2001;16:2274–7.PubMedCrossRef Frydman N, Romana S, Le Lorc’h M, Vekemans M, Frydman R, Tachjian G. Assisting reproduction of infertile men carrying a Robertsonian translocation. Hum Reprod. 2001;16:2274–7.PubMedCrossRef
10.
Zurück zum Zitat Moosani N, Pattinson HA, Carter MD, Cox DM, Rademaker AW, Martin RH. Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization. Fertil Steril. 1995;64:811–7.PubMed Moosani N, Pattinson HA, Carter MD, Cox DM, Rademaker AW, Martin RH. Chromosomal analysis of sperm from men with idiopathic infertility using sperm karyotyping and fluorescence in situ hybridization. Fertil Steril. 1995;64:811–7.PubMed
11.
Zurück zum Zitat Anton E, Blanco J, Egoscue J, Vidal F. Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q10). Hum Reprod. 2004;19:1345–51.PubMedCrossRef Anton E, Blanco J, Egoscue J, Vidal F. Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q10). Hum Reprod. 2004;19:1345–51.PubMedCrossRef
12.
Zurück zum Zitat World Health Organization. Laboratory manual for the examination of human semen and sperm-cervical mucus interaction. New York: Cambridge University Press; 1999. World Health Organization. Laboratory manual for the examination of human semen and sperm-cervical mucus interaction. New York: Cambridge University Press; 1999.
13.
Zurück zum Zitat Pelloster F, Sèle B, Jalbert H. Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation. Hum Genet. 1987;85:116–20.CrossRef Pelloster F, Sèle B, Jalbert H. Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation. Hum Genet. 1987;85:116–20.CrossRef
14.
Zurück zum Zitat Ogur G, Van Assche E, Vegetti W, Verheyen G, Tournaye H, Bonduelle M, et al. Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers. Mol Hum Reprod. 2006;12:209–15.PubMedCrossRef Ogur G, Van Assche E, Vegetti W, Verheyen G, Tournaye H, Bonduelle M, et al. Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers. Mol Hum Reprod. 2006;12:209–15.PubMedCrossRef
15.
Zurück zum Zitat Escudero T, Lee M, Carrel D, Blanco J, Munne S. Analysis of chromosomes abnormalities in sperm and embryos from two 45, XY, t(13;14)(q10;q10) carriers. Prenat Diagn. 2000;20:599–602.PubMedCrossRef Escudero T, Lee M, Carrel D, Blanco J, Munne S. Analysis of chromosomes abnormalities in sperm and embryos from two 45, XY, t(13;14)(q10;q10) carriers. Prenat Diagn. 2000;20:599–602.PubMedCrossRef
16.
Zurück zum Zitat Martin RH. Cytogenetic analysis of sperm from a male heterozygous for a 13 ;14 Robertsonian translocation. Hum Genet. 1988;80:357–61.PubMedCrossRef Martin RH. Cytogenetic analysis of sperm from a male heterozygous for a 13 ;14 Robertsonian translocation. Hum Genet. 1988;80:357–61.PubMedCrossRef
17.
Zurück zum Zitat Ogawa S, Araki S, Araki Y, Ohno M, Sato I. Chromosome analysis of human spermatozoa from an oligoasthenozoospermic carrier for a 13;14 Robertsonian translocation by their injection into mouse oocytes. Hum Reprod. 2000;15:1136–9.PubMedCrossRef Ogawa S, Araki S, Araki Y, Ohno M, Sato I. Chromosome analysis of human spermatozoa from an oligoasthenozoospermic carrier for a 13;14 Robertsonian translocation by their injection into mouse oocytes. Hum Reprod. 2000;15:1136–9.PubMedCrossRef
18.
Zurück zum Zitat Luciani JM, Guichaoua MR, Mattei A, Morazzani MR. Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle. Cytogenet Cell Genet. 1984;38:14–22.PubMedCrossRef Luciani JM, Guichaoua MR, Mattei A, Morazzani MR. Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle. Cytogenet Cell Genet. 1984;38:14–22.PubMedCrossRef
19.
Zurück zum Zitat Morel F, Roux C, Bresson JL. FISH analysis of the chromosomal status of spermatozoa from three men with 45, XY, der (13;14)(q10;q10). Mol Hum Reprod. 2001;7:483–8.PubMedCrossRef Morel F, Roux C, Bresson JL. FISH analysis of the chromosomal status of spermatozoa from three men with 45, XY, der (13;14)(q10;q10). Mol Hum Reprod. 2001;7:483–8.PubMedCrossRef
20.
Zurück zum Zitat Vegetti W, Van Asseche E, Frias A, Verheven G, Bianchi MM, Bonduelle M, et al. Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in-situ hybridization in infertile men. Hum Reprod. 2000;15:351–65.PubMedCrossRef Vegetti W, Van Asseche E, Frias A, Verheven G, Bianchi MM, Bonduelle M, et al. Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in-situ hybridization in infertile men. Hum Reprod. 2000;15:351–65.PubMedCrossRef
21.
Zurück zum Zitat Luciani JM, Guichaoua MR. L’incidence des anomalies chromosomiques de structure sur la spermatogenèse chez l’homme. Reprod Nutr Dev. 1990;1:95–103. Luciani JM, Guichaoua MR. L’incidence des anomalies chromosomiques de structure sur la spermatogenèse chez l’homme. Reprod Nutr Dev. 1990;1:95–103.
22.
Zurück zum Zitat Vendrell JM, Garcia F, Veiga A, Calderon G, Egozcue S, Egozcue J, et al. Meiotic abnormalities and spermatogenic parameters in severe oligoasthenozoospermia. Hum Reprod. 1999;14:375–8.PubMedCrossRef Vendrell JM, Garcia F, Veiga A, Calderon G, Egozcue S, Egozcue J, et al. Meiotic abnormalities and spermatogenic parameters in severe oligoasthenozoospermia. Hum Reprod. 1999;14:375–8.PubMedCrossRef
23.
Zurück zum Zitat Blanco J, Egoscue J, Vidal F. interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei. Hum Genet. 2000;106:500–5.PubMedCrossRef Blanco J, Egoscue J, Vidal F. interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei. Hum Genet. 2000;106:500–5.PubMedCrossRef
24.
Zurück zum Zitat Guttenbach M, Martinez-Exposito MJ, Michelmann HW, Engel W, Schmid M. Incidence of diploid and disomic sperm nuclei in 45 infertile men. Hum Reprod. 1997;12:468–73.PubMedCrossRef Guttenbach M, Martinez-Exposito MJ, Michelmann HW, Engel W, Schmid M. Incidence of diploid and disomic sperm nuclei in 45 infertile men. Hum Reprod. 1997;12:468–73.PubMedCrossRef
25.
Zurück zum Zitat Estop AM, Cieply K, Munne S, Surti U, Wakim A, Feingold E. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies. Hum Genet. 2000;106:517–24.PubMedCrossRef Estop AM, Cieply K, Munne S, Surti U, Wakim A, Feingold E. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies. Hum Genet. 2000;106:517–24.PubMedCrossRef
26.
Zurück zum Zitat Pang MG, Hoegerman SF, Cuticchia AJ, Moon SY, Doncel GF, Acosta AA, et al. Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection. Hum Reprod. 1999;14:1266–73.PubMedCrossRef Pang MG, Hoegerman SF, Cuticchia AJ, Moon SY, Doncel GF, Acosta AA, et al. Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection. Hum Reprod. 1999;14:1266–73.PubMedCrossRef
27.
Zurück zum Zitat Rives N, Saint Clair A, Mazurier S, Sibert L, Simeon N, Joly G, et al. Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males. Hum Genet. 1999;105:266–72.PubMedCrossRef Rives N, Saint Clair A, Mazurier S, Sibert L, Simeon N, Joly G, et al. Relationship between clinical phenotype, semen parameters and aneuploidy frequency in sperm nuclei of 50 infertile males. Hum Genet. 1999;105:266–72.PubMedCrossRef
Metadaten
Titel
Chromosomal segregation in spermatozoa of five Robertsonian translocation carriers t(13;14)
verfasst von
Manel Mahjoub
Meriem Mehdi
Sonia Brahem
Hatem Elghezal
Samira Ibala
Ali Saad
Publikationsdatum
01.07.2011
Verlag
Springer US
Erschienen in
Journal of Assisted Reproduction and Genetics / Ausgabe 7/2011
Print ISSN: 1058-0468
Elektronische ISSN: 1573-7330
DOI
https://doi.org/10.1007/s10815-011-9560-6

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