DNA methylation signatures in mendelian developmental disorders as a diagnostic bridge between genotype and phenotype. (15th March 2019)

• Record Type: Journal Article
• Authors: Sadikovic, Bekim; Aref-Eshghi, Erfan; Levy, Michael A; Rodenhiser, David
• Is Part Of: Epigenomics. Volume 11:Number 5(2019)
• Page Start: 563
• Page End: 575
• Publication Date: 2019-03-15
• Subjects: clinical applications -- developmental disability -- DNA methylation -- epigenetics and disease -- episignature -- intellectual disability -- microarray; Epigenesis -- Periodicals; Genomics -- Periodicals; Chromatin -- Periodicals; DNA -- Periodicals; 572.87
• DOI: 10.2217/epi-2018-0192
• Languages: English
• ISSNs: 1750-1911

Abstract

Epigenetic and genetic mechanisms regulate the establishment and maintenance of gene expression in its proper context. Recent genome-wide mapping approaches have identified DNA methylation (DNAm) signatures in patients clinically diagnosed with syndromes manifesting as developmental disabilities with intellectual impairments. Here, we review recent studies in which these DNA methylation signatures have enabled highly sensitive and specific screening of such individuals and have clarified ambiguous cases where subjects present with genetic sequence variants of unknown clinical significance (VUS). We propose that these episignatures be considered as echoes and/or legacies of the initiating mutational events within proteins of the so-called epigenetic machinery. As well, we discuss approaches to directly confirm the functional consequences and the implications of these episignatures to patient management and treatment.