Aberrant DNA methylation in lymphocytes of children with neurodevelopmental disorders

• Published in: Russian journal of genetics Vol. 53; no. 11; pp. 1243 - 1258
• Main Authors: Naumova, O. Yu, Rychkov, S. Yu, Odintsova, V. V., Kornilov, S. A., Shabalina, E. V., Antsiferova, D. V., Zhukova, O. V., Grigorenko, E. L.
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01.11.2017
• Subjects: Animal Genetics and Genomics; Biomedical and Life Sciences; Biomedicine; Human Genetics; Microbial Genetics and Genomics; peripheral blood lymphocytes; genome-wide DNA methylation; Illumina HumanMethylation450; encephalopathy; differential methylation; epigenetics
• ISSN: 1022-7954; 1608-3369
• DOI: 10.1134/S1022795417110072

Recent research in the field of genomics and epigenetics has provided evidence that alterations in the system of epigenetic regulation are highly involved in the molecular etiology of neurodegenerative and neuropathic disorders. However, there is a gap in knowledge on the epigenetic perturbations that may accompany the CNS impairments during the development in the prenatal period and their manifestation as a congenital encephalopathy in the early postnatal period of child development. The present study is one of the first attempts aimed at addressing this gap. Here, we present data on genome-wide profiles of DNA methylation obtained using the Illumina HumanMethylation450 microarray in peripheral blood cells in a sample of young children (up to four years of age) diagnosed with congenital encephalopathy. We provide evidence on systematic alterations in the epigenome—predominant hypermethylation of gene promoter associated CpG islands—related to the CNS impairment in children. Specifically, we found significant DNA methylation changes in genes involved in DNA-dependent transcription regulation and transcription factor binding, with a key role of the transcription factor JUN ; in genes controlling cellular response to hypoxia; and in genes involved in the control of neuronal development, functioning, and death.