Hypomethylation of Wnt signaling regulator genes in developmental language disorder

Author:

Iype Mary1,Melempatt Nisha2,James Jesmy3,Thomas Sanjeev V14,Anitha Ayyappan3ORCID

Affiliation:

1. Dept. of Neurology, Institute for Communicative & Cognitive Neurosciences (ICCONS), Thiruvananthapuram, 695 011, Kerala, India

2. Dept. of Audiology & Speech Language Pathology, ICCONS, Shoranur, Palakkad, 679 523, Kerala, India

3. Dept. of Neurogenetics, ICCONS, Shoranur, Palakkad, 679 523, Kerala, India

4. Dept. of Neurology, ICCONS, Shoranur, Palakkad, 679 523, Kerala, India

Abstract

Background: Developmental language disorder (DLD) is a neurodevelopmental disorder. Considering the pivotal role of epigenetics in neurodevelopment, we examined any altered DNA methylation between DLD and control subjects. Materials & methods: We looked into genome-wide methylation differences between DLD and control groups. The findings were validated by quantitative PCR (qPCR). Results: In the DLD group, differential methylation of CpG sites was observed in the Wnt signaling regulator genes APCDD1, AMOTL1, LRP5, MARK2, TMEM64, TRABD2B, VEPH1 and WNT2B. Hypomethylation of APCDD1, LRP5 and WNT2B was confirmed by qPCR. Conclusion: This is the first report associating Wnt signaling with DLD. The findings are relevant in the light of the essential role of Wnt in myelination, and of the altered myelination in DLD.

Funder

Science and Engineering Research Board

Publisher

Informa UK Limited

Subject

Cancer Research,Genetics

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