VODICKA, R., R. VRTEL, Ladislav DUŠEK, A.R. SINGH, K. KRIZOVA, V. SVACINOVA, V. HORINOVA, J. DOSTAL, I. OBORNA, J. BREZINOVA, A. SOBEK a J. SANTAVY. TSPY gene copy number as a potential new risk factor for male infertility. Reproductive Biomedicine Online. 2007, roč. 14, č. 5, s. 579-587, 8 s. ISSN 1472-6491.
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Základní údaje
Originální název TSPY gene copy number as a potential new risk factor for male infertility
Název česky TSPY gene copy number as a potential new risk factor for male infertility
Autoři VODICKA, R. (203 Česká republika), R. VRTEL (203 Česká republika), Ladislav DUŠEK (203 Česká republika, garant), A.R. SINGH (203 Česká republika), K. KRIZOVA (203 Česká republika), V. SVACINOVA (203 Česká republika), V. HORINOVA (203 Česká republika), J. DOSTAL (203 Česká republika), I. OBORNA (203 Česká republika), J. BREZINOVA (203 Česká republika), A. SOBEK (203 Česká republika) a J. SANTAVY (203 Česká republika).
Vydání Reproductive Biomedicine Online, 2007, 1472-6491.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30214 Obstetrics and gynaecology
Stát vydavatele Velká Británie a Severní Irsko
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 2.840
Kód RIV RIV/00216224:14110/07:00040020
Organizační jednotka Lékařská fakulta
UT WoS 000246445000009
Klíčová slova anglicky capillary electrophoresis; male infertility; multicopy gene; quantitative fluorescence PCR; TSPY gene; Y chromosome
Štítky Capillary electrophoresis, male infertility, multicopy gene, quantitative fluorescence PCR, TSPY gene, Y chromosome
Změnil Změnil: prof. RNDr. Ladislav Dušek, Ph.D., učo 670. Změněno: 1. 4. 2010 08:44.
Anotace
The human TSPY (testis-specific protein, Y-linked) gene family (30-60 copies) is situated in the MSY (male-specific) region of the Y chromosome. Testis-specific expression indicates that the gene plays a role in spermatogenesis. Refined quantitative fluorescence PCR (polymerase chain reaction) was applied to evaluate the relative number of TSPY copies compared with AMELY/X (amelogenin gene, Y-linked) genes in 84 stratified infertile men and in 40 controls. A significantly higher number of TSPY copies was found in infertile men compared with the controls (P = 0.002). The diagnostic discrimination potential of the relative number of TSPY copies was evaluated by receiver operating characteristic curve analysis. TSPY/AMELY was unambiguously found to be powerful in the diagnostic separation of both the control samples and the infertile men, reaching a good level of specificity (0.642) and sensitivity (0.732) at a cut-off point of 0.46. The findings were supported by independently repeated studies of randomly selected positive samples and controls. Evaluation of the TSPY copy number offers a completely new diagnostic approach in relation to the genetic cause of male infertility. The possible effect of the copy number of TSPY genes on spermatogenesis may explain indiscrete pathological alterations of spermatid quality and quantity.
Anotace česky
The human TSPY (testis-specific protein, Y-linked) gene family (30-60 copies) is situated in the MSY (male-specific) region of the Y chromosome. Testis-specific expression indicates that the gene plays a role in spermatogenesis. Refined quantitative fluorescence PCR (polymerase chain reaction) was applied to evaluate the relative number of TSPY copies compared with AMELY/X (amelogenin gene, Y-linked) genes in 84 stratified infertile men and in 40 controls. A significantly higher number of TSPY copies was found in infertile men compared with the controls (P = 0.002). The diagnostic discrimination potential of the relative number of TSPY copies was evaluated by receiver operating characteristic curve analysis. TSPY/AMELY was unambiguously found to be powerful in the diagnostic separation of both the control samples and the infertile men, reaching a good level of specificity (0.642) and sensitivity (0.732) at a cut-off point of 0.46. The findings were supported by independently repeated studies of randomly selected positive samples and controls. Evaluation of the TSPY copy number offers a completely new diagnostic approach in relation to the genetic cause of male infertility. The possible effect of the copy number of TSPY genes on spermatogenesis may explain indiscrete pathological alterations of spermatid quality and quantity.
Návaznosti
NR8442, projekt VaVNázev: Standardizace a individualizace léčby testikulárních germinálních nádorů (příprava centralizace veškeré péče do dvou center v ČR)
Investor: Ministerstvo zdravotnictví ČR, Standardizace a individualizace léčby testikulárních germinálních nádorů (příprava centralizace veškeré péče do dvou center v ČR
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