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Methylation of the SLC6a2 gene promoter in major depression and panic disorder

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posted on 2024-07-26, 14:21 authored by Richard Bayles, Emma K. Baker, Jeremy B M Jowett, David Barton, Murray Esler, Assam El-Osta, Gavin LambertGavin Lambert
Reduced function of the noradrenaline transporter (NET) has been demonstrated in patients with major depressive disorder (MDD) and panic disorder. Attempts to explain NET dysfunction in MDD and panic disorder by genetic variation in the NET gene SLC6a2 have been inconclusive. Transcriptional silencing of the SLC6a2 gene may be an alternative mechanism which can lead to NET dysfunction independent of DNA sequence. The objective of this study was to characterise the DNA methylation state of the SLC6a2 gene promoter in patients with MDD and panic disorder. SLC6a2 promoter methylation was also analysed before and after antidepressant treatment. This study was performed with DNA from blood, using bisulphite sequencing and EpiTYPER methylation analyses. Patients with MDD or panic disorder were not found to differ significantly from healthy controls in the pattern of methylation of the SLC6a2 gene promotor. While significant correlations between methylation levels at some CpG sites and physiological measures were identified, overall the variation in DNA methylation between patients was small, and the significance of this variation remains equivocal. No significant changes in SLC6a2 promoter methylation were observed in response to antidepressant treatment. Further in-depth analysis of alternative mechanisms of transcriptional regulation of the SLC6a2 gene in human health and disease would be of value.

Funding

National Health and Medical Research Council

Government of Victoria

Baker IDI Heart and Diabetes Institute

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PDF (Published version)

ISSN

1932-6203

Journal title

PLoS ONE

Volume

8

Issue

12

Article number

article no. e83223

Pagination

e83223-

Publisher

Public Library of Science (PLoS)

Copyright statement

Copyright © 2013. Bayles et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Language

eng

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