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Published in: Journal of Assisted Reproduction and Genetics 1/2012

01-01-2012 | Genetics

Meiotic segregation and interchromosomal effects in a rare (1:2:10) complex chromosomal rearrangement

Authors: Gordon Kirkpatrick, Sai Ma

Published in: Journal of Assisted Reproduction and Genetics | Issue 1/2012

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Abstract

Purpose

Complex chromosomal rearrangements (CCR) are rare rearrangements involving more than two chromosomes and more than two breakpoints. CCR are associated with male infertility as a result of the disruption of spermatogenesis due to complex meiotic configurations and the production of chromosomally abnormal sperm. We examined a carrier of a t(1:2:10) CCR in order to determine the patterns of segregation and any presence of an interchromosomal effect (ICE).

Methods

Centromeric, locus specific and telomeric probes (Vysis, USA) were used for the study. On ~1,000 sperm nuclei from the reciprocal translocation carrier, dual color Fluorescence in situ hybridization (FISH) was performed on each of the involved chromosomes to determine the patterns of segregation. FISH was also performed on chromosome 13, 18, 21, X and Y to determine any ICE.

Results

We observed abnormal chromosome complements in 24.3%, 19.5% and 15.8% of sperm for chromosomes 2, 10 and 1, respectively. There was a significantly increased rate of ICEs for chromosomes 13 and 21 when compared with controls.

Conclusions

CCR may present a lower risk for producing unbalanced chromosomes than other studies have indicated. CCRs may be at an increased risk for ICE especially among acrocentric chromosomes.
Literature
1.
go back to reference Pai GS, Thomas GH, Mahoney W, Migeon BR. Complex chromosome rearrangements. Report of a new case and literature review. Clin Genet. 1980;18:436–44.PubMedCrossRef Pai GS, Thomas GH, Mahoney W, Migeon BR. Complex chromosome rearrangements. Report of a new case and literature review. Clin Genet. 1980;18:436–44.PubMedCrossRef
2.
go back to reference Sadallah N, Hulten M. A complex three breakpoint translocation involving chromosomes 2, 4, and 9 identified by meiotic investigations of a human male ascertained for subfertility. Hum Genet. 1985;71:312–20.CrossRef Sadallah N, Hulten M. A complex three breakpoint translocation involving chromosomes 2, 4, and 9 identified by meiotic investigations of a human male ascertained for subfertility. Hum Genet. 1985;71:312–20.CrossRef
3.
go back to reference Johannisson R, Lohrs U, Passarge E. Pachytene analysis in males heterozygous for a familial translocation (9;12;13)(q22;q22;q32) ascertained through a child with partial trisomy 9. Cytogenet Cell Genet. 1988;47:160–6.PubMedCrossRef Johannisson R, Lohrs U, Passarge E. Pachytene analysis in males heterozygous for a familial translocation (9;12;13)(q22;q22;q32) ascertained through a child with partial trisomy 9. Cytogenet Cell Genet. 1988;47:160–6.PubMedCrossRef
4.
go back to reference Kovacs A, Villagomez DA, Gustavsson I, Lindblad K, Foote RH, Howard TH. Synaptonemal complex analysis of a three-breakpoint translocation in a subfertile bull. Cytogenet Cell Genet. 1992;61:195–201.PubMedCrossRef Kovacs A, Villagomez DA, Gustavsson I, Lindblad K, Foote RH, Howard TH. Synaptonemal complex analysis of a three-breakpoint translocation in a subfertile bull. Cytogenet Cell Genet. 1992;61:195–201.PubMedCrossRef
5.
go back to reference Lejeune J. Autosomal Disorders Pediatrics. 1963;32:326–37. Lejeune J. Autosomal Disorders Pediatrics. 1963;32:326–37.
6.
go back to reference Tang SS, Gao H, Robinson WP, Ho Yuen B, Ma S. An association between sex chromosomal aneuploidy in sperm and an abortus with 45, X of paternal origin: possible transmission of chromosomal abnormalities through ICSI. Hum Reprod. 2004;19:147–51.PubMedCrossRef Tang SS, Gao H, Robinson WP, Ho Yuen B, Ma S. An association between sex chromosomal aneuploidy in sperm and an abortus with 45, X of paternal origin: possible transmission of chromosomal abnormalities through ICSI. Hum Reprod. 2004;19:147–51.PubMedCrossRef
7.
go back to reference Kirkpatrick G, Ferguson KA, Gao H, Tang S, Chow V, Yuen BH, et al. A comparison of sperm aneuploidy rates between infertile men with normal and abnormal karyotypes. Hum Reprod. 2008;23:1679–83.PubMedCrossRef Kirkpatrick G, Ferguson KA, Gao H, Tang S, Chow V, Yuen BH, et al. A comparison of sperm aneuploidy rates between infertile men with normal and abnormal karyotypes. Hum Reprod. 2008;23:1679–83.PubMedCrossRef
8.
go back to reference Cifuentes P, Navarro J, Miguez L, Egozcue J, Benet J. Sperm segregation analysis of a complex chromosome rearrangement, 2;22;11, by whole chromosome painting. Cytogenet Cell Genet. 1998;82:204–9.PubMedCrossRef Cifuentes P, Navarro J, Miguez L, Egozcue J, Benet J. Sperm segregation analysis of a complex chromosome rearrangement, 2;22;11, by whole chromosome painting. Cytogenet Cell Genet. 1998;82:204–9.PubMedCrossRef
9.
go back to reference Pellestor F, Anahory T, Lefort G, Puechberty J, Liehr T, Hédon B, et al. Complex chromosomal rearrangements: origin and meiotic behavior. Hum Reprod Update. 2011;4:476–94.CrossRef Pellestor F, Anahory T, Lefort G, Puechberty J, Liehr T, Hédon B, et al. Complex chromosomal rearrangements: origin and meiotic behavior. Hum Reprod Update. 2011;4:476–94.CrossRef
10.
go back to reference Loup V, Bernicot I, Janssens P, Hedon B, Hamamah S, Pellestor F, et al. Combined FISH and PRINS sperm analysis of complex chromosome rearrangement t(1;19;13): an approach facilitating PGD. Mol Hum Reprod. 2010;16:111–6.PubMedCrossRef Loup V, Bernicot I, Janssens P, Hedon B, Hamamah S, Pellestor F, et al. Combined FISH and PRINS sperm analysis of complex chromosome rearrangement t(1;19;13): an approach facilitating PGD. Mol Hum Reprod. 2010;16:111–6.PubMedCrossRef
11.
go back to reference Lu PY, Hammitt DG, Zinsmeister AR, Dewald GW. Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8)(q23;q27;p21). Fertil Steril. 1994;62:394–9.PubMed Lu PY, Hammitt DG, Zinsmeister AR, Dewald GW. Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8)(q23;q27;p21). Fertil Steril. 1994;62:394–9.PubMed
12.
go back to reference Lespinasse J, Rethore MO, North MO, Bovier-Lapierre M, Lundsteen C, Fert-Ferrer, et al. Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases. Ann Genet. 2004;47:315–24.PubMedCrossRef Lespinasse J, Rethore MO, North MO, Bovier-Lapierre M, Lundsteen C, Fert-Ferrer, et al. Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases. Ann Genet. 2004;47:315–24.PubMedCrossRef
13.
go back to reference Ferguson KA, Chow V, Ma S. Silencing of unpaired meiotic chromosomes and altered recombination patterns in an azoospermic carrier of a t(8;13) reciprocal translocation. Hum Reprod. 2008;23:988–95.PubMedCrossRef Ferguson KA, Chow V, Ma S. Silencing of unpaired meiotic chromosomes and altered recombination patterns in an azoospermic carrier of a t(8;13) reciprocal translocation. Hum Reprod. 2008;23:988–95.PubMedCrossRef
14.
go back to reference Coco R, Rahn MI, Estanga PG, Antonioli G, Solari AJ. A constitutional complex chromosome rearrangement involving meiotic arrest in an azoospermic male: case report. Hum Reprod. 2004;19:2784–90.PubMedCrossRef Coco R, Rahn MI, Estanga PG, Antonioli G, Solari AJ. A constitutional complex chromosome rearrangement involving meiotic arrest in an azoospermic male: case report. Hum Reprod. 2004;19:2784–90.PubMedCrossRef
16.
go back to reference Eaker S, Pyle A, Cobb J, Handel MA. Evidence for meiotic spindle checkpoint from analysis of spermatocytes from Robertsonian-chromozome heterozygous mice. J Cell Sci. 2001;114:2953–65.PubMed Eaker S, Pyle A, Cobb J, Handel MA. Evidence for meiotic spindle checkpoint from analysis of spermatocytes from Robertsonian-chromozome heterozygous mice. J Cell Sci. 2001;114:2953–65.PubMed
Metadata
Title
Meiotic segregation and interchromosomal effects in a rare (1:2:10) complex chromosomal rearrangement
Authors
Gordon Kirkpatrick
Sai Ma
Publication date
01-01-2012
Publisher
Springer US
Published in
Journal of Assisted Reproduction and Genetics / Issue 1/2012
Print ISSN: 1058-0468
Electronic ISSN: 1573-7330
DOI
https://doi.org/10.1007/s10815-011-9655-0

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