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. 2011 Apr;96(4):E674-9.
doi: 10.1210/jc.2010-2018. Epub 2011 Jan 20.

Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions

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Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions

Carolina J Jorgez et al. J Clin Endocrinol Metab. 2011 Apr.

Abstract

Context: The pseudoautosomal regions (PARs) of the Y-chromosome undergo meiotic recombination with the X-chromosome. PAR mutations are associated with infertility and mental and stature disorders.

Objective: The aim of the study was to determine whether men with Y-chromosome microdeletions have structural defects in PARs.

Design and participants: Eighty-seven infertile men with Y-chromosome microdeletions and 35 controls were evaluated for chromosomal rearrangements using commercial or custom (X- and Y-chromosome) array comparative genomic hybridization or by quantitative PCR of selected PAR genes. Multisoftware-defined chromosomal gains or losses were validated by quantitative PCR and FISH.

Results: Array comparative genomic hybridization confirmed the AZF deletions identified by multiplex PCR. All men with Y-chromosome microdeletions and an abnormal karyotype displayed PAR abnormalities, as did 10% of men with Y-chromosome microdeletions and a normal karyotype. None of the control subjects or infertile men without Y-chromosome microdeletions had PAR duplications or deletions. SHOX aberrations occurred in 14 men (nine gains and five losses); four were short in stature (<10th percentile), and one was tall (>95th percentile). In contrast, the height of 23 men with Y-chromosome microdeletions and normal PARs was average at 176.8 cm (50th percentile).

Conclusions: Y-chromosome microdeletions can include PAR defects causing genomic disorders such as SHOX, which may be transmitted to offspring. Previously unrecognized PAR gains and losses in men with Y-chromosome microdeletions may have consequences for offspring.

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Figures

Fig. 1.
Fig. 1.
SHOX duplication associated with abnormal stature in AZFbc infertile men. A, Demographics of four of the AZFbc patients with SHOX duplication. B, FISH analysis on subject 57658 [46,X,del(Y)(q11.2)] validated duplication on PAR1 and it localized on Yq. Probe RP11-1325A17 (includes SHOX) is shown in red, whereas control probe RP11-611P22 on the X chromosome is shown in green. C, View of aCGH of subject 61783 [46,X,idic(Yq11.2)] Y-chromosome showing a loss on Yq11.223-Yq11.23 that corresponds to the AZFbc region. Blue dots represent the relative hybridization to each probe in the aCGH.

References

    1. Stahl PJ, Masson P, Mielnik A, Marean MB, Schlegel PN, Paduch DA. 2010. A decade of experience emphasizes that testing for Y microdeletions is essential in American men with azoospermia and severe oligozoospermia. Fertil Steril 94:1753–1756 - PubMed
    1. Silber SJ, Alagappan R, Brown LG, Page DC. 1998. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. Hum Reprod 13:3332–3337 - PubMed
    1. Oates RD, Silber S, Brown LG, Page DC. 2002. Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI. Hum Reprod 17:2813–2824 - PubMed
    1. Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, Cordum HS, Hillier L, Brown LG, Repping S, Pyntikova T, Ali J, Bieri T, Chinwalla A, Delehaunty A, Delehaunty K, Du H, Fewell G, Fulton L, Fulton R, Graves T, Hou SF, Latrielle P, Leonard S, Mardis E, Maupin R, McPherson J, Miner T, Nash W, Nguyen C, Ozersky P, Pepin K, Rock S, Rohlfing T, Scott K, Schultz B, Strong C, Tin-Wollam A, Yang SP, Waterston RH, Wilson RK, Rozen S, Page DC. 2003. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 423:825–837 - PubMed
    1. Gabriel-Robez O, Rumpler Y, Ratomponirina C, Petit C, Levilliers J, Croquette MF, Couturier J. 1990. Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X;Y translocation. Cytogenet Cell Genet 54:38–42 - PubMed

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