| Literature DB >> 28352654 |
Abdul Waheed Khan1,2,3, Mark Ziemann1,2, Susan J Corcoran2, Harikrishnan K N1,2,3, Jun Okabe1,2, Haloom Rafehi1,2, Scott S Maxwell1,2, Murray D Esler2, Assam El-Osta1,2,3,4.
Abstract
While strongly implicated in postural tachycardia syndrome (POTS), considerable controversy exists regarding norepinephrine transporter (NET) loss of function. POTS is characterized by the clinical symptoms of orthostatic intolerance, lightheadedness, tachycardia, and syncope or near syncope with upright posture. Abnormal sympathetic nervous system activity is typical, of a type which suggests dysfunction of the NET, with evidence that the gene responsible is under tight epigenetic control. Using RNA of isolated chromatin combined with massive parallel sequencing (RICh-seq) we show that let-7i miRNA suppresses NET by methyl-CpG-binding protein 2 (MeCP2). Vorinostat restores epigenetic control and NET expression in leukocytes derived from POTS participants.Entities:
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Year: 2017 PMID: 28352654 PMCID: PMC5358482 DOI: 10.1172/jci.insight.90183
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708