Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis

Monica Miozzo, Carlo F Selmi, Barbara Gentilin, Francesca R. Grati, Silvia Sirchia, Sabine Oertelt, Massimo Zuin, M. Eric Gershwin, Mauro Podda, Pietro Invernizzi

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102 Scopus citations

Abstract

Recent work has demonstrated enhanced X monosomy in women with primary biliary cirrhosis (PBC) as well as two other female-predominant autoimmune diseases, systemic sclerosis and autoimmune thyroid disease. To further our understanding of these events, we have investigated the mechanisms of X chromosome loss and X chromosome inactivation (XCI) in 166 women with PBC and 226 rigorously age-matched healthy and liver disease controls. X chromosome analysis and determination of loss pattern was performed by quantitative fluorescent polymerase chain reaction (QF-PCR) with 4 X-linked short tandem repeats. Further definition of the XCI was based on analysis of methylation-sensitive restriction sites. Importantly, in PBC the X chromosome loss occurs not only more frequently but also in a preferential fashion. This observation supports our thesis that the enhanced X monosomy involves only one parentally derived chromosome and is not secondary to a constitutive non random pattern of XCI. In fact, in the presence of monosomy, the lost X chromosome is necessarily the inactive homologue. Conclusion: The finding that the X chromosome loss is preferential suggests the critical involvement of X chromosome gene products in the female predisposition to PBC and also emphasizes the need to determine the parental origin of the maintained chromosome to investigate the role of imprinting.

Original languageEnglish (US)
Pages (from-to)456-462
Number of pages7
JournalHepatology
Volume46
Issue number2
DOIs
StatePublished - Aug 2007

ASJC Scopus subject areas

  • Hepatology

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    Miozzo, M., Selmi, C. F., Gentilin, B., Grati, F. R., Sirchia, S., Oertelt, S., Zuin, M., Gershwin, M. E., Podda, M., & Invernizzi, P. (2007). Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis. Hepatology, 46(2), 456-462. https://doi.org/10.1002/hep.21696