Stable variants of sperm aneuploidy among healthy men show associations between germinal and somatic aneuploidy
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S.
Grantová podpora
P42 ES004705
NIEHS NIH HHS - United States
PubMed
11992257
PubMed Central
PMC379139
DOI
10.1086/340791
PII: S0002-9297(07)60703-4
Knihovny.cz E-zdroje
- MeSH
- aneuploidie * MeSH
- diploidie MeSH
- dospělí MeSH
- genetická variace genetika MeSH
- hybridizace in situ fluorescenční MeSH
- lidé MeSH
- lidské chromozomy, pár 8 genetika MeSH
- lymfocyty cytologie metabolismus patologie MeSH
- motilita spermií genetika MeSH
- počet spermií MeSH
- pohlavní chromozomy genetika MeSH
- spermie cytologie metabolismus patologie MeSH
- velikost buňky MeSH
- zdraví MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
- srovnávací studie MeSH
Repeated semen specimens from healthy men were analyzed by sperm fluorescence in situ hybridization (FISH), to identify men who consistently produced elevated frequencies of aneuploid sperm and to determine whether men who were identified as stable variants of sperm aneuploidy also exhibited higher frequencies of aneuploidy in their peripheral blood lymphocytes. Seven semen specimens were provided by each of 15 men over a 2-year period and were evaluated by the X-Y-8 multicolor sperm FISH method (i.e., approximately 1,050,000 sperm were analyzed from 105 specimens). Three men were identified as stable aneuploidy variants producing significantly higher frequencies of XY, disomy X, disomy Y, disomy 8, and/or diploid sperm over time. In addition, one man and three men were identified as sperm-morphology and sperm-motility variants, respectively. Strong correlations were found between the frequencies of sperm with autosomal and sex-chromosome aneuploidies and between the two types of meiosis II diploidy; but not between sperm aneuploidy and semen quality. A significant association was found between the frequencies of sex-chromosome aneuploidies in sperm and lymphocytes in a subset of 10 men (r2=0.67, P=.004), especially between XY sperm and sex-chromosome aneuploidy in lymphocytes (r2=0.70, P=.003). These findings suggest that certain apparently healthy men can produce significantly higher frequencies of both aneuploid sperm and lymphocytes. Serious long-term somatic and reproductive health consequences may include increased risks of aneuploidy-related somatic diseases and of having children with paternally transmitted aneuploidies, such as Klinefelter, Turner, triple-X, and XYY syndromes.
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Abruzzo MA, Griffin DK, Millie EA, Sheean LA, Hassold TJ (1996) The effect of y-chromosome alpha-satellite array length on the rate of sex chromosome disomy in human sperm. Hum Genet 97:819–823 PubMed
Amalfitano G, Chatel M, Paquis P, Michiels JF (2000) Fluorescence in situ hybridization study of aneuploidy of chromosomes 7, 10, X, and Y in primary and secondary glioblastomas. Cancer Genet Cytogenet 116:6–9 PubMed
Baumgartner A, Schmid TE, Schuetz CG, Adler ID (2001) Detection of aneuploidy in rodent and human sperm by multicolor FISH after chronic exposure to diazepam. Mutat Res 490:11–19 PubMed
Baumgartner A, Van Hummelen P, Lowe XR, Adler ID, Wyrobek AJ (1999) Numerical and structural chromosomal abnormalities detected in human sperm with a combination of multicolor FISH assays. Environ Mol Mutagen 33:49–58 PubMed
Bielanska M, Tan SL, Ao A (2000) Fluorescence in-situ hybridization of sex chromosomes in spermatozoa and spare preimplantation embryos of a Klinefelter 46,XY/47,XXY male. Hum Reprod 15:440–444 PubMed
Blanco J, Gabau E, Gómez D, Baena N, Guitart M, Egozcue J, Vidal F (1998) Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21 in a population with a high prevalence of Down’s syndrome: increased incidence in cases of paternal origin. Am J Hum Genet 63:1067–1072 PubMed PMC
Brandriff B, Gordon L (1990) Human sperm cytogenetics and the one-cell zygote. In: Allen JW, Bridges BA, Lyon MF, Moses MJ, Russell LB (eds) Biology of mammalian germ cell mutagenesis. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, pp 183–194
Catalan J, Autio K, Wessman M, Lindholm C, Knuutila S, Sorsa M, Norppa H (1995) Age associated micronuclei containing centromeres and the X chromosome in lymphocytes of women. Cytogenet Cell Genet 68:11–33 PubMed
Colombero LT, Hariprashad JJ, Tsai MC, Rosenwaks Z, Palermo GD (1999) Incidence of sperm aneuploidy in relation to semen characteristics and assisted reproductive outcome. Fertil Steril 72:90–96 PubMed
Dasari VK, Goharderakhshan RZ, Perinchery G, Li LC, Tanaka Y, Alonzo J, Dahiya R (2001) Expression analysis of Y chromosome genes in human prostate cancer. J Urol 165:1335–1341 PubMed
De Mas P, Daudin M, Vincent MC, Bourrouillou G, Calvas P, Mieusset R, Bujan L (2001) Increased aneuploidy in spermatozoa from testicular tumour patients after chemotherapy with cisplatin, etoposide and bleomycin. Hum Reprod 16:1204–1208 PubMed
Devi AS, Metzger DA, Luciano AA, Benn PA (1998) 45, X/46, XX mosaicism in patients with idiopathic premature ovarian failure. Fertil Steril 70:89–93 PubMed
Downie SE, Flaherty SP, Swann NJ, Matthews CD (1997) Estimation of aneuploidy for chromosomes 3, 7, 16, X and Y in spermatozoa from 10 normospermic men using fluorescence in-situ hybridization. Mol Hum Reprod 3:815–819 PubMed
Duesberg P, Rasnick D (2000) Aneuploidy, the somatic mutation that makes cancer a species of its own. Cell Motil Cytoskeleton 47:81–107 PubMed
Duesberg P, Rasnick D, Li RH, Winters L, Rausch C, Hehlmann R (1999) How aneuploidy may cause cancer and genetic instability. Anticancer Res 19:4887–4906 PubMed
Eskenazi B, Wyrobek AJ, Kidd SA, Lowe X, Moore DII, Weisinger, K, Aylstock M (2002) Sperm aneuploidy in fathers of children with paternally and maternally inherited Klinefelter syndrome. Hum Reprod 17:576–583 PubMed
Fait G, Yogev L, Botchan A, Paz G, Lessing JB, Yavetz H (2001) Sex chromosome aneuploidy in sperm cells obtained from Hodkin’s lymphoma patients before therapy. Fertil Steril 75:828–829 PubMed
Galloway SM, Buckton KE (1978) Aneuploidy and ageing: chromosome studies on a random sample of the population using G-banding. Cytogenet Cell Genet 20:78–95 PubMed
Gazvani MR, Wilson EDA, Richmond DH, Howard PJ, Kingsland CR, Lewis-Jones DI (2000a) Evaluation of the role of mitotic instability in karyotypically normal men with oligozoospermia. Fertil Steril 73:51–55 PubMed
——— (2000b) Role of mitotic control in spermatogenesis. Fertil Steril 74:251–256 PubMed
Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ (1995) Non-disjunction in human sperm: evidence for an effect of increasing paternal age. Hum Mol Genet 4:2227–2232 PubMed
Hamilton LC (1998) Statistics with STATA 5. Brooks/Cole Publishing, Pacific Grove, CA
Harkonen K, Viitanen T, Larsen SB, Bonde JP, Lahdetie J (1999) Aneuploidy in sperm and exposure to fungicides and lifestyle factors. Environ Mol Mutagen 34:39–46 PubMed
Hassold T, Hunt P (2001) To err (meiotically) is human: the genesis of human aneuploidy. Nat Rev Genet 2:280–291 PubMed
Kinakin B, Rademaker A, Martin R (1997) Paternal age effect of YY aneuploidy in human sperm, as by fluorescence in situ hybridization. Cytogenet Cell Genet 78:116–119 PubMed
Lim AST, Fong Y, Yu SL (1999a) Analysis of the sex chromosome constitution of sperm in men with a 47,XYY mosaic karyotype by fluorescence in situ hybridization. Fertil Steril 72:121–123 PubMed
——— (1999b) Estimates of sperm sex chromosome disomy and diploidy rates in a 47,XXY/46,XY mosaic Klinefelter patient. Hum Genet 104:405–409 PubMed
Lowe X, Collins B, Allen J, Titenko Holland N, Breneman J, van Beek M, Bishop J, Wyrobek AJ (1995) Aneuploidies and micronuclei in the germ cells of male mice of advanced age. Mutat Res 338:59–76 PubMed
Lowe X, Eskenazi B, Nelson DO, Kidd S, Alme A, Wyrobek AJ (2001) Frequency of XY sperm increases with age in fathers of boys with Klinefelter syndrome. Am J Hum Genet 69:1046–1054 PubMed PMC
Marchetti F, Bishop JB, Lowe X, Generoso WM, Hozier J, Wyrobek AJ (2001) Etoposide induces heritable chromosomal aberrations and aneuploidy during male meiosis in the mouse. Proc Natl Acad Sci USA 98:3952–3957 PubMed PMC
Martin RH, Chan K, Ko E, Rademaker AW (1994) Detection of aneuploidy in human sperm by fluorescence in situ hybridization (FISH): different frequencies in fresh and stored sperm nuclei. Cytogenet Cell Genet 65:95–96 PubMed
Martin RH, Rademaker A (1990) The frequency of aneuploidy among individual chromosomes in 6,821 human sperm chromosome complements. Cytogenet Cell Genet 53:103–107 PubMed
——— (1995) Reliability of aneuploidy estimates in human sperm: results of fluorescence in situ hybridization studies using two different scoring criteria. Mol Reprod Dev 42:89–93 PubMed
Martin RH, Spriggs E, Ko E, Rademaker AW (1995) The relationship between paternal age, sex ratios, and aneuploidy frequencies in human sperm, as assessed by multicolor FISH. Am J Hum Genet 57:1395–1399 PubMed PMC
Martínez-Pasarell O, Nogués C, Bosch M, Egoscue J, Templado C (1999) Analysis of sex chromosome aneuploidy in sperm from fathers of Turner syndrome patients. Hum Genet 104:345–349 PubMed
Morel F, Mercier S, Roux C, Elmrini T, Clavequin MC, Bresson JL (1998) Interindividual variations in the disomy frequencies of human spermatozoa and their correlation with nuclear maturity as evaluated by aniline blue staining. Fertil Steril 69:1122–1127 PubMed
Morel F, Roux C, Bresson JL (2000) Segregation of sex chromosomes in spermatozoa of 46,XY/47,XXY men by multicolour fluorescence in-situ hybridization. Mol Hum Reprod 6:566–570 PubMed
Nash RN, Willalt LR, Andrew T, Green AJ (1997) Recurrent multiple aneuploidies: a family with autosomal recessive failure of mitotic control. J Med Genet Suppl 34:63
Pang MG, Hoegerman SF, Cuticchia AJ, Moon SY, Doncel GF, Acosta AA, Kearns WG (1999) 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 14:1266–1273 PubMed
Papi L, Montali E, Marconi G, Guazzelli R, Bigozzi U, Maraschio P, Zuffardi O (1989) Evidence for a human mitotic mutant with pleiotropic effect. Ann Hum Genet 53:243–248 PubMed
Pfeffer J, Pang MG, Hoegerman SF, Osgood CJ, Stacey MW, Mayer J, Oehninger S, Kearns WG (1999) Aneuploidy frequencies in semen fractions from ten oligoasthenoteratozoospermic patients donating sperm for intracytoplasmic sperm injection. Fertil Steril 72:472–478 PubMed
Rives N, Joly G, Machy A, Simeon N, Leclerc P, Mace B (2000) Assessment of sex chromosome aneuploidy in sperm nuclei from 47,XXY and 46,XY/47,XXY males: comparison with fertile and infertile males with normal karyotype. Mol Hum Reprod 6:107–112 PubMed
Robbins WA (1996) Cytogenetic damage measured in human sperm following cancer chemotherapy. Mutat Res 355:235–252 PubMed
Robbins WA, Baulch JE, Moore D, Weier HU, Blakey D, Wyrobek AJ (1995) Three-probe fluorescence in situ hybridization to assess chromosome X, Y, and 8 aneuploidy in sperm of 14 men from two healthy groups: evidence for a paternal age effect on sperm aneuploidy. Reprod Fertil Dev 7:799–809 PubMed
Robbins WA, Meistrich ML, Moore D, Hagemeister FB, Weier HU, Cassel MJ, Wilson G, Eskenazi B, Wyrobek AJ (1997a) Chemotherapy induces transient sex chromosomal and autosomal aneuploidy in human sperm. Nat Genet 16:74–78 PubMed
Robbins WA, Rubes J, Selevan, SG, Perreault, SD (1999) Air pollution and sperm aneuploidy in healthy young men. Environ Epidemiol Toxicol 1:125–131
Robbins WA, Segraves R, Pinkel D, Wyrobek AJ (1993) Detection of aneuploid human sperm by fluorescence in situ hybridization—evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y. Am J Hum Genet 52:799–807 PubMed PMC
Robbins WA, Vine MF, Truong KY, Everson RB (1997b) Use of fluorescence in situ hybridization (FISH) to assess effects of smoking, caffeine, and alcohol on aneuploidy load in sperm of healthy men. Environ Mol Mutagen 30:175–183 PubMed
Rubes J, Lowe X, Moore D, Perreault S, Slott V, Evenson D, Selevan SG, Wyrobek AJ (1998) Smoking cigarettes is associated with increased sperm disomy in teenage men. Fertil Steril 70:715–723 PubMed
Schmid TE, Lowe X, Marchetti F, Bishop J, Haseman J, Wyrobek AJ (2001) Evaluation of inter-scorer and inter-laboratory reliability of the mouse epididymal sperm aneuploidy (m-ESA) assay. Mutagenesis 16:189–195 PubMed
Schultz H, Mennicke K, Schlieker H, Alhasani S, Balspratsch M, Diedrich K, Schwinger E (2000) Comparative study of disomy and diploidy rates in spermatozoa of fertile and infertile men: a donor-adapted protocol for multi-colour fluorescence in situ hybridization (FISH). Int J Androl 23:300–308 PubMed
Selevan SG, Borkovec L, Slott VL, Zudová Z, Rubes J, Evenson DP, Perreault SD (2000) Semen quality and reproductive health of young Czech men exposed to seasonal air pollution. Environ Health Perspect 108:887–894 PubMed PMC
Sen S (2000) Aneuploidy and cancer. Curr Opin Oncol 12:82–88 PubMed
Shi QH, Ko E, Barclay L, Hoang T, Rademaker A, Martin R (2001) Cigarette smoking and aneuploidy in human sperm. Mol Reprod Dev 59:417–421 PubMed
Shi Q, Martin RH (2000a) Aneuploidy in human sperm: a review of the frequency and distribution of aneuploidy, effects of donor age and lifestyle factors. Cytogenet Cell Genet 90:219–226 PubMed
——— (2000b) Spontaneous frequencies of aneuploid and diploid sperm in 10 normal Chinese men: assessed by multicolor fluorescence in situ hybridization. Cytogenet Cell Genet 90:79–83 PubMed
Sloter ED, Lowe X, Moore DH, Nath J, Wyrobek AJ (2000) Multicolor FISH analysis of chromosomal breaks, duplications, deletions, and numerical abnormalities in the sperm of healthy men. Am J Hum Genet 67:862–872 PubMed PMC
Soares SR, Templado C, Blanco J, Egozcue J, Vidal F (2001) Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunction. Hum Genet 108:134–139 PubMed
Spriggs EL, Rademaker AW, Martin RH (1995) Aneuploidy in human sperm: results of two- and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X, and Y. Cytogenet Cell Genet 71:47–53 PubMed
Tolmie JL, Boyd E, Batstare P, Fergusson-Smith ME, Al Roomi L, Connor JM (1988) Siblings with chromosome mosaicism, microcephaly and growth retardation: the phenotypic expression of a human mitotic mutant? Hum Genet 80:197–200 PubMed
Van Hummelen P, Lowe XR, Wyrobek AJ (1996) Simultaneous detection of structural and numerical chromosome abnormalities in sperm of healthy men by multicolor fluorescence in situ hybridization. Hum Genet 98:608–615 PubMed
Van Hummelen P, Manchester D, Lowe X, Wyrobek AJ (1997) Meiotic segregation, recombination, and gamete aneuploidy assessed in a t(1;10)(p22.1;q22.3) reciprocal translocation carrier by three- and four-probe multicolor FISH in sperm. Am J Hum Genet 61:651–659 PubMed PMC
Vegetti W, Vanassche E, Frias A, Verheyen G, Bianchi MM, Bonduelle M, Liebaers I, Vansteirteghem A (2000) Correlation between semen parameters and sperm aneuploidy rates investigated by fluorescence in-situ hybridization in infertile men. Hum Reprod 15:351–365 PubMed
Verma RS, Babu A (1989) Human chromosomes: manual of basic techniques, Pergamon Press, New York, pp 4–9
Wang JY, Samura O, Zhen DK, Cowan JM, Cardone V, Summers M, Bianchi DW (2000) Fluorescence in-situ hybridization analysis of chromosomal constitution in spermatozoa from a mosaic 47, XYY/46,XY male. Mol Hum Reprod 6:665–668 PubMed
World Health Organization (1992) WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge University Press, Cambridge
World Health Organization (1999) WHO laboratory manual for the examination of human semen and semen-cervical mucus interaction. Cambridge University Press, Cambridge
Wyrobek AJ, Aardema M, Eichenlaubritter U, Ferguson L, Marchetti F (1996) Mechanisms and targets involved in maternal and paternal age effects on numerical aneuploidy. Environ Mol Mutagen 28:254–264 PubMed
Wyrobek AJ, Marchetti F, Sloter E, Bishop J (2000) Chromosomally defective sperm and their developmental consequences. In: Anderson D, Karakaya AE, Srám RJ (eds) Human monitoring after environmental and occupational exposure to chemical and physical agents. IOS Press, Amsterdam, pp 134–150
Yamaki H, Sasano H, Ohashi Y, Shizawa S, Shineha R, Satomi S, Nagura H (2001) Alteration of X and Y chromosomes in human esophageal squamous cell carcinoma. Anticancer Res 21:985–990 PubMed