PCR for rapid detection of nine loci of Y-chromosomal DNA including SRY sequences in Turner syndrome patients
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Abstract
Detection of Y-chromosomal sequences is crucial for certain cases of phenotypic females since prophylactic gonadectomy is recommended to prevent germ cell tumor development in the future. This cross-sectional study aimed to develop a simple, rapid, and accurate method for determination of 9 loci of Y-chromosomal DNA spanning Yp, centromere, and Yq, including SRY sequences by using 2 polymerase chain reaction (PCR) conditions. The first PCR condition was used for Assay A, which yielded pentaplex PCR products consisting of loci ZFX/ZFY, SRY, AZFz, AZFb, and AZFc. The second PCR condition was used for Assay B, which yielded PCR products consisting loci PABY, AMGLXX/AMGLXY, Y-centromere, and YD. DNA from 20 Turner syndrome (TS) patients with different chromosomal aberrations were assessed. Normal female DNA and normal male DNA were used as controls. The pentaplex PCR together with 4 other simultaneous PCR reactions showed 10 positive PCR products of 9 loci in normal male controls and 3 mosaic TS patients (45,X/46,XY and 45,X/46,X,+marker). Five positive PCR products representing the regions PABY, ZFX/ZFY, and AMGLXX/AMGLXY and SRY were identified in 1 of 9 TS (monosomy; 45,X) patients. All female controls, 8 TS patients with monosomy X, and 8 mosaic TS patients with only X chromosome aberrations showed positive results for loci ZFX/ZFY and AMGLXX. The developed PCR conditions were demonstrated to accurately and rapidly detect 9 Y-chromosomal fragments including SRY sequences in TS patients.
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References
Hargreave TB. Genetic basis of male infertility. British Medical Bulletin. 2000;56(3): 650-671.
Pryor JL, Kent-First M, Muallem A, Van Bergen AH, Nolten WE, Meisner L, et al. Microdeletions in the Y chromosome of infertile men. N Engl J Med. 1997;336(8):534-539.
Gholami D, Jafari-Ghahfarokhi H, Nemati-Dehkordi M, Teimori H. Y chromosome microdeletions frequency in idiopathic azoospermia, oligoasthenozoospermia, and oligospermia. Int J Reprod BioMed. 2017;15(11):703-712.
Wikipedia. Catergory: genes on human Y chromosome [Internet]. 2018 [cited 2018 Jan 20] Available from https://en.wikipedia.org/wiki/Y_chromosome.
Lo KW, Lam SK, Cheung TH, Wong SP, Chang A. Chow JH. Gonadoblastoma in patient with Turner’s syndrome. J Obstet Gynecol Res. 1996;22(1):35-41.
de Marqui AB, da Silva-Grecco RL, Balarin MA. Prevalence of Y-chromosome sequences and gonadoblastoma in Turner syndrome. Rev Paul Pediatr. 2016;34(1):114-121.
Muroya K, Ishii T, Nakahori Y, Asakura Y, Tachibana K, Masuno M, et al. Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: molecular analysis in four patients. Gene Chromosome Cancer. 1999;25(1):40-45.
Fernandes S, Ventura V, Dória S, Barros A. Y-chromosome detection in Turner syndrome. Human Genet Embryol. 2013;3(3):115.
Assumpcao JG, Hackel C, Marques-de-Faria AP, Palandi de MM. Molecular mapping of an Idic(Yp) chromosome in an Ulrich-Turner patient. Am J Med Genet. 2000;91(2):95-98.
Barbosa AS, Ferraz-Costa TE, Semer M, Liberman B, Moreira-Filho CA. XY gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the Y chromosome involving the SRY gene. Hum Genet. 1995;95(1):63-66.
Choi SK, Kim JW, Park SY, Kim YM, Kim JM, Ryu HM, et al. Retroactive DNA analysis for sex determination and dystrophin gene by polymerase chain reaction with archived cytogenetic slides. Exp Mol Med. 1999;31(1):36-41.
Ellis N, Kidd J, Goodfellow PJ, Kidd K, Goodfellow PN. Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary. Am J Hum. Genet. 1990;46(5):950-955.
Modi D, Shah C, Sachdeva G, Gadkar S, Bhartiya D, Puri C. Ontogeny and cellular localization of SRY transcripts in the human testes and its detection in spermatozoa. Reproduction. 2005;130(5):603-613.
Berta P, Hawkins JR, Sinclair AH, Taylor A, Griffiths BL, Goodfellow PN, et al. Genetic evidence equating SRY and the testis-determining factor. Nature. 1990;348(6300):448-450.
Akane A, Shiono H, Matsubara K, Nakahori Y, Seki S, Nagafuchi S, et al. Sex identification of forensic specimens by polymerase chain reaction (PCR): two alternative methods. Forensic Sci Int. 1991;49(1):8188.
Nakahori Y, Hamano K, Iwaya M, Nakagome Y. Sex identification by polymerase chain reaction using XY homologous primer. Am J Med Genet. 1991;39(4):472-473.
Nagafuchi S, Seki S, Nakahori Y, Tamura T, Numabe H, Nakagome Y. PCR detection of structurally abnormal Y chromosomes. Jpn J Hum Genet. 1992;37(3):187-193.
Prafulla S. Ambulkar , Ramji Sigh, MVR Reddy, Poonam S. Varma, Dilip O. Gupta, Moreshwar R Shende, et al. Genetic risk of azoospermia factor (AZF) microdeletions in Idiopathic cases of azoospermia and oligozoospermia in central Indian population. J Clin Diagn Res. 2014;8(3):88-91.
Simoni M, Gromoll J, Dworniczak B, Rolf C, Abshagen K, Kamischke A, et al. Screening for deletions of the Y chromosome involving the DAZ (deleted in azoospermia) gene in azoospermia and severe oligozoospermia. Fertil Steril. 1997;67(3):542-547.
Tse JY, Yeung WS, Ng EH, Cheng LN, Zhu HB, Teng XM, et al. A comparative study of Y chromosome microdeletions in infertile males from two Chinese populations. J Assist Reprod Genet. 2002;19(8):376-383.
Yamaguchi A, Fukushi M, Kikuchi Y, Aparicio J, Wakisaka A. A simple method for gender verification based on PCR detection of Y-chromosomal DNA and its application at the Winter Universiade 1991 in Sapporo City, Japan. Int J Sports Med. 1992;13(4):304-307.
Rooney DE, Czepulkowski BH. Human chromosome preparation, essential techniques series. In: Rickwood D, editor. Department of Biological and Chemical Sciences,University of Essex. Wivenhoe Park, Colchester, UK: University Press; 1997. p. 37-38.
Sambrook J, Fritschi EF, Maniatis T. Molecular cloning a laboratory manual. Cold Spring Harbor Laboratory Press, New York, USA. 1989.
ISCN 2016: International System for Human Cytogenomic Nomenclature (2016) in J. McGowan-Jordan, A. Simon, M. Schmid, editor. Cytogenetic Genome Res. 2016; 149: 1-2.
Freriks K, Timmers HJ, Netea-Maier RT, Beerendonk CC, Otten BJ, van Alfen-van der Velden JA, et al. Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome. Eur J Med Genet. 2013;56(9):497-501.
Shankar RK, Backeljauw PF. Current best practice in the management of Turner syndrome. Ther Adv Endocrinol Metab. 2018;9(1):33-40.
Sallai Á, Sólyom J, Dobos M, Szabó J, Halász Z, Ságodi L, et al. Y-chromosome markers in Turner syndrome: screening of 130 patients. J Endocrinol Invest. 2010;33(4):222-227.
Rojek A, Obara-Moszynska M, Kolesinska Z, Rabska-Pietrzak B, Niedziela M. Molecular detection and incidence of Y chromosomal material in patients with Turner syndrome. Sex Dev. 2017;11(5-6):254-261.
Knauer-Fischer S, Besikoglu B, Inta I, Kneppo C, Vogt PH, Bettendorf M. Analyses of gonadoblastoma Y (GBY)-locus and of Y centromere in Turner syndrome patients. Exp Clin Endocrinol Diabetes. 2015;123(1):61-65.
Bianco B, Lipay MV, Guedes AD, Verreschi IT. Clinical implications of the detection of Y-chromosome mosaicism in Turner's syndrome: report of 3 cases. Fertil Steril. 2008;90(4):1197:e17-e20.