Microdeletions in the Y Chromosome of Infertile Men
Jon L. Pryor, M.D., Marijo Kent-First, Ph.D., Ariege Muallem, B.S., Andrew H. Van Bergen, B.S., Wolfram E. Nolten, M.D., Lorraine Meisner, Ph.D., and Kenneth P. Roberts, Ph.D.
Background Some infertile men with azoospermia or severe oligospermiahave small deletions in regions of the Y chromosome. However,the frequency of such microdeletions among men with infertilityin general is unknown. We sought to determine the prevalenceof Y-chromosome microdeletions among infertile men and to correlatethe clinical presentation of the men with specific deletions.
Methods We studied 200 consecutive infertile men. Each man wasevaluated comprehensively for known causes of infertility, andY-chromosome microdeletions were studied with use of the polymerasechain reaction to amplify specific regions of the chromosome.The Y chromosomes of 200 normal men were also analyzed.
Results Fourteen infertile men (7 percent) and four normal men(2 percent) had microdeletions of the Y chromosome. Nine ofthe infertile men had azoospermia or severe oligospermia (spermconcentration, <5 million per milliliter), four had oligospermia(sperm concentration, 5 million to <20 million per milliliter),and one had normospermia (sperm concentration, >20 millionper milliliter). The size and location of the deletions variedand did not correlate with the severity of spermatogenic failure.The fathers of six infertile men with microdeletions were studied;two had the same deletions as their sons, and four had no deletions.
Conclusions A small proportion of men with infertility haveY-chromosome microdeletions, but the size and position of thedeletions correlate poorly with the severity of spermatogenicfailure, and a deletion does not preclude the presence of viablesperm and possible conception.
Source Information
From the Departments of Urologic Surgery (J.L.P., A.H.V.B., K.P.R.), Cell Biology and Neuroanatomy (J.L.P., K.P.R.), and Obstetrics and Gynecology (J.L.P.), University of Minnesota Medical School, Minneapolis; the Promega Corporation, Madison, Wis. (M.K.-F., A.M.); and the Departments of Meat and Animal Science (A.M.), Medicine (W.E.N.), and Preventive Medicine (L.M.), University of Wisconsin, Madison.
Address reprint requests to Dr. Roberts at the Department of Urologic Surgery, Box 394 UMHC, 420 Delaware St. S.E., Minneapolis, MN 55455.
Abu-Musa, A. A., Nassar, A. H., Usta, I. M.
(2008). Attitude of women with IVF and spontaneous pregnancies towards prenatal screening. Hum Reprod
23: 2438-2443
[Abstract][Full Text]
Bowdin, S., Allen, C., Kirby, G., Brueton, L., Afnan, M., Barratt, C., Kirkman-Brown, J., Harrison, R., Maher, E. R, Reardon, W.
(2007). A survey of assisted reproductive technology births and imprinting disorders. Hum Reprod
22: 3237-3240
[Abstract][Full Text]
Hadjkacem-Loukil, L., Ayadi, I., Bahloul, A., Ayadi, H., Ammar-Keskes, L.
(2007). Tag STS in the AZF Region Associated With Azoospermia in a Tunisian Population. J Androl
28: 652-658
[Abstract][Full Text]
Gallardo, T. D., John, G. B., Shirley, L., Contreras, C. M., Akbay, E. A., Haynie, J. M., Ward, S. E., Shidler, M. J., Castrillon, D. H.
(2007). Genomewide Discovery and Classification of Candidate Ovarian Fertility Genes in the Mouse. Genetics
177: 179-194
[Abstract][Full Text]
Bhasin, S.
(2007). Approach to the Infertile Man. J. Clin. Endocrinol. Metab.
92: 1995-2004
[Abstract][Full Text]
Kleiman, S.E., Yogev, L., Hauser, R., Botchan, A., Maymon, B.B.-S., Paz, G., Yavetz, H.
(2007). Expression profile of AZF genes in testicular biopsies of azoospermic men. Hum Reprod
22: 151-158
[Abstract][Full Text]
Hellani, A., Al-Hassan, S., Al-Duraihim, A., Coskun, S.
(2005). Y chromosome microdeletions: are they implicated in teratozoospermia?. Hum Reprod
20: 3505-3509
[Abstract][Full Text]
Seli, E., Sakkas, D.
(2005). Spermatozoal nuclear determinants of reproductive outcome: implications for ART. Hum Reprod Update
11: 337-349
[Abstract][Full Text]
Lynch, M., Cram, D.S., Reilly, A., O'Bryan, M.K., Baker, H.W.G., de Kretser, D.M., McLachlan, R.I.
(2005). The Y chromosome gr/gr subdeletion is associated with male infertility. Mol Hum Reprod
11: 507-512
[Abstract][Full Text]
Stouffs, K., Lissens, W., Tournaye, H., Van Steirteghem, A., Liebaers, I.
(2005). The choice and outcome of the fertility treatment of 38 couples in whom the male partner has a Yq microdeletion. Hum Reprod
20: 1887-1896
[Abstract][Full Text]
Hewitson, L.
(2004). Primate models for assisted reproductive technologies. Reproduction
128: 293-299
[Abstract][Full Text]
Benoff, S. H., Millan, C., Hurley, I. R., Napolitano, B., Marmar, J. L.
(2004). Bilateral increased apoptosis and bilateral accumulation of cadmium in infertile men with left varicocele. Hum Reprod
19: 616-627
[Abstract][Full Text]
Rao, L., Babu, A., Kanakavalli, M., Padmalatha, V., Singh, A., Singh, P. K., Deenadayal, M., Singh, L.
(2004). Chromosomal Abnormalities and Y Chromosome Microdeletions in Infertile Men With Varicocele and Idiopathic Infertility of South Indian Origin. J Androl
25: 147-153
[Abstract][Full Text]
Leslie, G.I., Gibson, F.L., McMahon, C., Cohen, J., Saunders, D.M., Tennant, C.
(2003). Children conceived using ICSI do not have an increased risk of delayed mental development at 5 years of age. Hum Reprod
18: 2067-2072
[Abstract][Full Text]
Hopps, C.V., Mielnik, A., Goldstein, M., Palermo, G.D., Rosenwaks, Z., Schlegel, P.N.
(2003). Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regions. Hum Reprod
18: 1660-1665
[Abstract][Full Text]
Thangaraj, K., Gupta, N. J., Pavani, K., Reddy, A. G., Subramainan, S., Rani, D. S., Ghosh, B., Chakravarty, B., Singh, L.
(2003). Y Chromosome Deletions in Azoospermic Men in India. J Androl
24: 588-597
[Abstract][Full Text]
Thangaraj, K., Joshi, M. B., Reddy, A. G., Rasalkar, A. A., Singh, L.
(2003). Sperm Mitochondrial Mutations as a Cause of Low Sperm Motility. J Androl
24: 388-392
[Abstract][Full Text]
Moore, F. L., Jaruzelska, J., Fox, M. S., Urano, J., Firpo, M. T., Turek, P. J., Dorfman, D. M., Pera, R. A. R.
(2003). Human Pumilio-2 is expressed in embryonic stem cells and germ cells and interacts with DAZ (Deleted in AZoospermia) and DAZ-Like proteins. Proc. Natl. Acad. Sci. USA
100: 538-543
[Abstract][Full Text]
Pasqualotto, F. F., Lucon, A. M., Hallak, J., Goes, P. M., Saldanha, L. B., Arap, S.
(2003). Induction of spermatogenesis in azoospermic men after varicocele repair. Hum Reprod
18: 108-112
[Abstract][Full Text]
Teng, Y.-N., Lin, Y.-M., Lin, Y.-H., Tsao, S.-Y., Hsu, C.-C., Lin, S.-J., Tsai, W.-C., Kuo, P.-L.
(2002). Association of a Single-Nucleotide Polymorphism of the Deleted-in-Azoospermia-Like Gene with Susceptibility to Spermatogenic Failure. J. Clin. Endocrinol. Metab.
87: 5258-5264
[Abstract][Full Text]
Oates, R. D., Silber, S., Brown, L. G., Page, D. C.
(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
[Abstract][Full Text]
Zubenko, G. S., Stiffler, J. S., Hughes III, H. B., Fatigati, M. J., Zubenko, W. N.
(2002). Genome Survey for Loci That Influence Successful Aging: Sample Characterization, Method Validation, and Initial Results for the Y Chromosome. AJGP
10: 619-630
[Abstract][Full Text]
Luetjens, C.M., Gromoll, J., Engelhardt, M., von Eckardstein, S., Bergmann, M., Nieschlag, E., Simoni, M.
(2002). Manifestation of Y-chromosomal deletions in the human testis: a morphometrical and immunohistochemical evaluation. Hum Reprod
17: 2258-2266
[Abstract][Full Text]
Rolf, C., Gromoll, J., Simoni, M., Nieschlag, E.
(2002). Natural transmission of a partial AZFb deletion of the Y chromosome over three generations: Case report. Hum Reprod
17: 2267-2271
[Abstract][Full Text]
Tielemans, E., Burdorf, A., te Velde, E., Weber, R., van Kooij, R., Heederik, D.
(2002). Sources of Bias in Studies among Infertility Clients. Am J Epidemiol
156: 86-92
[Abstract][Full Text]
Zeyneloglu, H. B., Baltaci, V., Duran, H. E., Erdemli, E., Batioglu, S.
(2002). Achievement of pregnancy in globozoospermia with Y chromosome microdeletion after ICSI: Case report. Hum Reprod
17: 1833-1836
[Abstract][Full Text]
Kirsch, S, Weiss, B, Kleiman, S, Roberts, K, Pryor, J, Milunsky, A, Ferlin, A, Foresta, C, Matthijs, G, Rappold, G A
(2002). Localisation of the Y chromosome stature gene to a 700 kb interval in close proximity to the centromere. J. Med. Genet.
39: 507-513
[Full Text]
Katz, M.G., Chu, B., McLachlan, R., Alexopoulos, N.I., de Kretser, D.M., Cram, D.S.
(2002). Genetic follow-up of male offspring born by ICSI, using a multiplex fluorescent PCR-based test for Yq deletions. Mol Hum Reprod
8: 589-595
[Abstract][Full Text]
Gatta, V, Stuppia, L, Calabrese, G, Morizio, E, Guanciali-Franchi, P, Palka, G
(2002). A new case of Yq microdeletion transmitted from a normal father to two infertile sons. J. Med. Genet.
39: e27-27
[Full Text]
Kolettis, P. N.
(2002). The Evaluation and Management of the Azoospermic Patient. J Androl
23: 293-305
[Full Text]
Buonadonna, A.L., Cariola, F., Caroppo, E., Carlo, A.D., Fiorente, P., Valenzano, M.C., D'Amato, G., Gentile, M.
(2002). Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y;14 translocation and alternate centromere inactivation. Hum Reprod
17: 564-569
[Abstract][Full Text]
Peterlin, B., Kunej, T., Sinkovec, J., Gligorievska, N., Zorn, B.
(2002). Screening for Y chromosome microdeletions in 226 Slovenian subfertile men. Hum Reprod
17: 17-24
[Abstract][Full Text]
Jaruzelska, J., Korcz, A., Wojda, A., Jedrzejczak, P., Bierla, J., Surmacz, T., Pawelczyk, L., Page, D. C, Kotecki, M.
(2001). Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion. J. Med. Genet.
38: 798-802
[Full Text]
Calogero, A. E., Garofalo, M. R., Barone, N., De Palma, A., Vicari, E., Romeo, R., Tumino, S., D'Agata, R.
(2001). Spontaneous regression over time of the germinal epithelium in a Y chromosome-microdeleted patient: Case report. Hum Reprod
16: 1845-1848
[Abstract][Full Text]
Foresta, C., Moro, E., Ferlin, A.
(2001). Prognostic value of Y deletion analysis: The role of current methods. Hum Reprod
16: 1543-1547
[Abstract][Full Text]
Larriba, S., Bassas, L., Egozcue, S., Gimenez, J., Ramos, M. D., Briceno, O., Estivill, X., Casals, T.
(2001). Adenosine Triphosphate-Binding Cassette Superfamily Transporter Gene Expression in Severe Male Infertility. Biol. Reprod.
65: 394-400
[Abstract][Full Text]
Krausz, C., Rajpert-De Meyts, E., Frydelund-Larsen, L., Quintana-Murci, L., McElreavey, K., Skakkebaek, N. E.
(2001). Double-Blind Y Chromosome Microdeletion Analysis in Men with Known Sperm Parameters and Reproductive Hormone Profiles: Microdeletions Are Specific for Spermatogenic Failure. J. Clin. Endocrinol. Metab.
86: 2638-2642
[Abstract][Full Text]
Makrinou, E., Fox, M., Lovett, M., Haworth, K., Cameron, J. M., Taylor, K., Edwards, Y. H.
(2001). TTY2: A Multicopy Y-Linked Gene Family. Genome Res
11: 935-945
[Abstract][Full Text]
Krausz, C., McElreavey, K.
(2001). Y chromosome microdeletions in `fertile' males. Hum Reprod
16: 1306-1306
[Full Text]
Foresta, C., Moro, E., Ferlin, A.
(2001). Y Chromosome Microdeletions and Alterations of Spermatogenesis. Endocr. Rev.
22: 226-239
[Abstract][Full Text]
Kleiman, S.E., Maymon, B.B.-S., Yogev, L., Paz, G., Yavetz, H.
(2001). The prognostic role of the extent of Y microdeletion on spermatogenesis and maturity of Sertoli cells. Hum Reprod
16: 399-402
[Abstract][Full Text]
Simoni, M.
(2001). Molecular diagnosis of Y chromosome microdeletions in Europe: state-of-the-art and quality control. Hum Reprod
16: 402-409
[Abstract][Full Text]
Liow, S. L., Yong, E. L., Ng, S. C.
(2001). Prognostic value of Y deletion analysis: How reliable is the outcome of Y deletion analysis in providing a sound prognosis?. Hum Reprod
16: 9-12
[Abstract][Full Text]
Reijo, R. A., Dorfman, D. M., Slee, R., Renshaw, A. A., Loughlin, K. R., Cooke, H., Page, D. C.
(2000). DAZ Family Proteins Exist Throughout Male Germ Cell Development and Transit from Nucleus to Cytoplasm at Meiosis in Humans and Mice. Biol. Reprod.
63: 1490-1496
[Abstract][Full Text]
Blanco, P., Shlumukova, M., Sargent, C. A, Jobling, M. A, Affara, N., Hurles, M. E
(2000). Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism. J. Med. Genet.
37: 752-758
[Abstract][Full Text]
Sun, C., Skaletsky, H., Rozen, S., Gromoll, J., Nieschlag, E., Oates, R., Page, D. C.
(2000). Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses. Hum Mol Genet
9: 2291-2296
[Abstract][Full Text]
Saut, N., Terriou, P., Navarro, A., Levy, N., Mitchell, M. J.
(2000). The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility. Mol Hum Reprod
6: 789-793
[Abstract][Full Text]
Le Bourhis, C., Siffroi, J. P., McElreavey, K., Dadoune, J. P.
(2000). Y chromosome microdeletions and germinal mosaicism in infertile males. Mol Hum Reprod
6: 688-693
[Abstract][Full Text]
Krausz, C., Quintana-Murci, L., McElreavey, K.
(2000). Prognostic value of Y deletion analysis: What is the clinical prognostic value of Y chromosome microdeletion analysis?. Hum Reprod
15: 1431-1434
[Abstract][Full Text]
Foresta, C., Ferlin, A., Moro, E.
(2000). Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility. Hum Mol Genet
9: 1161-1169
[Abstract][Full Text]
Van Landuyt, L., Lissens, W., Stouffs, K., Tournaye, H., Liebaers, I., Van Steirteghem, A.
(2000). Validation of a simple Yq deletion screening programme in an ICSI candidate population. Mol Hum Reprod
6: 291-297
[Abstract][Full Text]
Venables, J.P., Elliott, D.J., Makarova, O.V., Makarov, E.M., Cooke, H.J., Eperon, I.C.
(2000). RBMY, a probable human spermatogenesis factor, and other hnRNP G proteins interact with Tra2{beta} and affect splicing. Hum Mol Genet
9: 685-694
[Abstract][Full Text]
Goodwin, L. O., Karabinus, D. S., Pergolizzi, R. G., Benoff, S.
(2000). L-type voltage-dependent calcium channel {alpha}-1C subunit mRNA is present in ejaculated human spermatozoa. Mol Hum Reprod
6: 127-136
[Abstract][Full Text]
Vogel, T., Speed, R.M., Teague, P., Cooke, H.J.
(1999). Mice with Y chromosome deletion and reduced Rbm genes on a heterozygous Dazl1 null background mimic a human azoospermic factor phenotype. Hum Reprod
14: 3023-3029
[Abstract][Full Text]
Chang, P. L., Sauer, M. V., Brown, S.
(1999). Y chromosome microdeletion in a father and his four infertile sons. Hum Reprod
14: 2689-2694
[Abstract][Full Text]
Krausz, C., Quintana-Murci, L., Barbaux, S., Siffroi, J.-P., Rouba, H., Delafontaine, D., Souleyreau-Therville, N., Arvis, G., Antoine, J. M., Erdei, E., Taar, J. P., Tar, A., Jeandidier, E., Plessis, G., Bourgeron, T., Dadoune, J.-P., Fellous, M., McElreavey, K.
(1999). A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility. J. Clin. Endocrinol. Metab.
84: 3606-3612
[Abstract][Full Text]
Foresta, C., Moro, E., Garolla, A., Onisto, M., Ferlin, A.
(1999). Y Chromosome Microdeletions in Cryptorchidism and Idiopathic Infertility. J. Clin. Endocrinol. Metab.
84: 3660-3665
[Abstract][Full Text]
M.Dorfman, D., R.Genest, D., Pera, R. A.R.
(1999). Human DAZL1 encodes a candidate fertility factor in women that localizes to the prenatal and postnatal germ cells. Hum Reprod
14: 2531-2536
[Abstract][Full Text]
Ferlin, A., Moro, E., Onisto, M., Toscano, E., Bettella, A., Foresta, C.
(1999). Absence of testicular DAZ gene expression in idiopathic severe testiculopathies. Hum Reprod
14: 2286-2292
[Abstract][Full Text]
Kamischke, A., Gromoll, J., Simoni, M., Behre, H.M., Nieschlag, E.
(1999). Transmission of a Y chromosomal deletion involving the deleted in azoospermia (DAZ) and chromodomain (CDY1) genes from father to son through intracytoplasmic sperm injection: Case report. Hum Reprod
14: 2320-2322
[Abstract][Full Text]
Sargent, C. A, Boucher, C. A, Kirsch, S., Brown, G., Weiss, B., Trundley, A., Burgoyne, P., Saut, N., Durand, C., Levy, N., Terriou, P., Hargreave, T., Cooke, H., Mitchell, M., Rappold, G. A, Affara, N. A
(1999). The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences. J. Med. Genet.
36: 670-677
[Abstract][Full Text]
Slee, R., Grimes, B., Speed, R. M., Taggart, M., Maguire, S. M., Ross, A., McGill, N. I., Saunders, P. T. K., Cooke, H. J.
(1999). A human DAZ transgene confers partial rescue of the mouse Dazl null phenotype. Proc. Natl. Acad. Sci. USA
96: 8040-8045
[Abstract][Full Text]
Ferlin, A., Moro, E., Garolla, A., Foresta, C.
(1999). Human male infertility and Y chromosome deletions: role of the AZF-candidate genes DAZ, RBM and DFFRY. Hum Reprod
14: 1710-1716
[Abstract][Full Text]
Krausz, C., Bussani-Mastellone, C., Granchi, S., McElreavey, K., Scarselli, G., Forti, G.
(1999). Screening for microdeletions of Y chromosome genes in patients undergoing intracytoplasmic sperm injection. Hum Reprod
14: 1717-1721
[Abstract][Full Text]
Page, D. C., Silber, S., Brown, L. G.
(1999). Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility. Hum Reprod
14: 1722-1726
[Abstract][Full Text]
Calogero, A. E., Garofalo, M. R., D'Agata, R.
(1999). Factors influencing the variable incidence of Y chromosome microdeletions in infertile patients. Hum Reprod
14: 275-275
[Full Text]
Kleiman, S.E., Yogev, L., Gamzu, R., Hauser, R., Botchan, A., Lessing, J.B., Paz, G., Yavetz, H.
(1999). Genetic evaluation of infertile men. Hum Reprod
14: 33-38
[Abstract][Full Text]
Tut, T. G., Ghadessy, F. J., Trifiro, M. A., Pinsky, L., Yong, E. L.
(1997). Long Polyglutamine Tracts in the Androgen Receptor Are Associated with Reduced Trans-Activation, Impaired Sperm Production, and Male Infertility. J. Clin. Endocrinol. Metab.
82: 3777-3782
[Abstract][Full Text]
Lahn, B. T., Page, D. C.
(1997). Functional Coherence of the Human Y Chromosome. Science
278: 675-680
[Abstract][Full Text]
de Kretser, D. M., Burger, H. G.
(1997). The Y Chromosome and Spermatogenesis. NEJM
336: 576-578
[Full Text]