Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome

• Published in: The international journal of biochemistry & cell biology 2009, Vol.41 (1), p.117-126
• Main Authors: Matarazzo, M.R., De Bonis, M.L., Vacca, M., Della Ragione, F., D’Esposito, M.
• Format: Article
• Language: English
• Subjects: Abnormalities, Multiple - genetics; Chromatin; Chromatin - chemistry; Chromatin - metabolism; Chromosome Aberrations; DNA Methylation; Facial Asymmetry - genetics; Humans; ICF syndrome; Immunologic Deficiency Syndromes - genetics; Models, Molecular; Nuclear architecture; Rett syndrome; Rett Syndrome - genetics; Rett Syndrome - metabolism; Syndrome
• ISSN: 1357-2725; 1878-5875
• DOI: 10.1016/j.biocel.2008.07.026

Spatial organisation of DNA into chromatin profoundly affects gene expression and function. The recent association of genes controlling chromatin structure to human pathologies resulted in a better comprehension of the interplay between regulation and function. Among many chromatin disorders we will discuss Rett and immunodeficiency, centromeric instability and facial anomalies (ICF) syndromes. Both diseases are caused by defects related to DNA methylation machinery, with Rett syndrome affecting the transduction of the repressive signal from the methyl CpG binding protein prototype, MeCP2, and ICF syndrome affecting the genetic control of DNA methylation, by the DNA methyltransferase DNMT3B. Rather than listing survey data, our aim is to highlight how a deeper comprehension of gene regulatory web may arise from studies of such pathologies. We also maintain that fundamental studies may offer chances for a therapeutic approach focused on these syndromes, which, in turn, may become paradigmatic for this increasing class of diseases.