Werler S, Poplinski A, Gromoll J, Wistuba J
Research article (journal) | Peer reviewedWe hypothesized that patients with Klinefelter's syndrome (KS) not only undergo X inactivation, but also that genes escape from inactivation. Their transcripts would constitute a significant difference, as male metabolism is not adapted to a 'female-like' gene dosage. We evaluated the expression of selected X-linked genes in our 41, XX(Y)* male mice to determine whether these genes escape inactivation and whether tissue-specific differences occur.Correct X inactivation was identified by Xist expression. Relative expression of X-linked genes was examined in liver, kidney and brain tissue by real-time PCR in adult XX(Y)* and XY* males and XX females.Expression of genes known to escape X inactivation was analysed. Relative mRNA levels of Pgk1 (control, X inactivated), and the genes Eif2s3x, Kdm5c, Ddx3x and Kdm6a escaping from X inactivation were quantified from liver, kidney and brain. Pgk1 mRNA expression showed no difference, confirming correct X inactivation. In kidney and liver, XX(Y)* males resembled the female expression pattern in all four candidate genes and were distinguishable from XY* males. Contrastingly, in brain tissue XX(Y)* males expressed all four genes higher than male and female controls.Altered expression of genes escaping X inactivation probably contributes directly to the XX(Y)* phenotype.
Gromoll, Jörg | Centre of Reproductive Medicine and Andrology |
Poplinski, Andreas Christoph | Centre of Reproductive Medicine and Andrology |
Werler, Steffi | Centre of Reproductive Medicine and Andrology |
Wistuba, Joachim | Centre of Reproductive Medicine and Andrology |