Literature DB >> 33445578

Elevated Expression of SLC6A4 Encoding the Serotonin Transporter (SERT) in Gilles de la Tourette Syndrome.

Mathis Hildonen1, Amanda M Levy1, Christina Dahl2, Victoria A Bjerregaard1, Lisbeth Birk Møller1,3, Per Guldberg2,4, Nanette M Debes5, Zeynep Tümer1,6.   

Abstract

Gilles de la Tourette syndrome (GTS) is a complex neurodevelopmental disorder characterized by motor and vocal tics. Most of the GTS individuals have comorbid diagnoses, of which obsessive-compulsive disorder (OCD) and attention deficit-hyperactivity disorder (ADHD) are the most common. Several neurotransmitter systems have been implicated in disease pathogenesis, and amongst these, the dopaminergic and the serotonergic pathways are the most widely studied. In this study, we aimed to investigate whether the serotonin transporter (SERT) gene (SLC6A4) was differentially expressed among GTS individuals compared to healthy controls, and whether DNA variants (the SERT-linked polymorphic region 5-HTTLPR, together with the associated rs25531 and rs25532 variants, and the rare Ile425Val variant) or promoter methylation of SLC6A4 were associated with gene expression levels or with the presence of OCD as comorbidity. We observed that SLC6A4 expression is upregulated in GTS individuals compared to controls. Although no specific genotype, allele or haplotype was overrepresented in GTS individuals compared to controls, we observed that the LAC/LAC genotype of the 5-HTTLPR/rs25531/rs25532 three-locus haplotype was associated with higher SLC6A4 mRNA expression levels in GTS individuals, but not in the control group.

Entities:  

Keywords:  5-HTT; GTS; Gilles de la Tourette syndrome; OCD; SERT; SLC6A4; expression; methylation; obsessive compulsive disorder; serotonin

Year:  2021        PMID: 33445578      PMCID: PMC7827645          DOI: 10.3390/genes12010086

Source DB:  PubMed          Journal:  Genes (Basel)        ISSN: 2073-4425            Impact factor:   4.096


  57 in total

1.  Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region.

Authors:  K P Lesch; D Bengel; A Heils; S Z Sabol; B D Greenberg; S Petri; J Benjamin; C R Müller; D H Hamer; D L Murphy
Journal:  Science       Date:  1996-11-29       Impact factor: 47.728

2.  Gilles de la Tourette syndrome is associated with hypermethylation of the dopamine D2 receptor gene.

Authors:  Kirsten R Müller-Vahl; Gesa Loeber; Alexandra Kotsiari; Linda Müller-Engling; Helge Frieling
Journal:  J Psychiatr Res       Date:  2016-11-12       Impact factor: 4.791

3.  Abnormal expression of dopamine and serotonin transporters associated with the pathophysiologic mechanism of Tourette syndrome.

Authors:  Li Jijun; Li Zaiwang; Li Anyuan; Wang Shuzhen; Qi Fanghua; Zhao Lin; Lv Hong
Journal:  Neurol India       Date:  2010 Jul-Aug       Impact factor: 2.117

4.  A human serotonin transporter mutation causes constitutive activation of transport activity.

Authors:  Fusun Kilic; Dennis L Murphy; Gary Rudnick
Journal:  Mol Pharmacol       Date:  2003-08       Impact factor: 4.436

5.  Constitutive activity of the serotonin2C receptor inhibits in vivo dopamine release in the rat striatum and nucleus accumbens.

Authors:  Philippe De Deurwaerdère; Sylvia Navailles; Kelly A Berg; William P Clarke; Umberto Spampinato
Journal:  J Neurosci       Date:  2004-03-31       Impact factor: 6.167

Review 6.  The role of atypical antipsychotics for treatment of Tourette's syndrome: an overview.

Authors:  Cathy L Budman
Journal:  Drugs       Date:  2014-07       Impact factor: 9.546

7.  "Hyperglutamatergic cortico-striato-thalamo-cortical circuit" breaker drugs alleviate tics in a transgenic circuit model of Tourette׳s syndrome.

Authors:  Eric J Nordstrom; Katie C Bittner; Michael J McGrath; Clinton R Parks; Frank H Burton
Journal:  Brain Res       Date:  2015-10-08       Impact factor: 3.252

Review 8.  Neurobiological basis of serotonin-dopamine antagonists in the treatment of Gilles de la Tourette syndrome.

Authors:  Thomas D L Steeves; Susan H Fox
Journal:  Prog Brain Res       Date:  2008       Impact factor: 2.453

9.  A novel, putative gain-of-function haplotype at SLC6A4 associates with obsessive-compulsive disorder.

Authors:  Jens R Wendland; Pablo R Moya; Matthew R Kruse; Renee F Ren-Patterson; Catherine L Jensen; Kiara R Timpano; Dennis L Murphy
Journal:  Hum Mol Genet       Date:  2007-11-30       Impact factor: 6.150

10.  Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.

Authors:  Lea K Davis; Dongmei Yu; Clare L Keenan; Eric R Gamazon; Anuar I Konkashbaev; Eske M Derks; Benjamin M Neale; Jian Yang; S Hong Lee; Patrick Evans; Cathy L Barr; Laura Bellodi; Fortu Benarroch; Gabriel Bedoya Berrio; Oscar J Bienvenu; Michael H Bloch; Rianne M Blom; Ruth D Bruun; Cathy L Budman; Beatriz Camarena; Desmond Campbell; Carolina Cappi; Julio C Cardona Silgado; Danielle C Cath; Maria C Cavallini; Denise A Chavira; Sylvain Chouinard; David V Conti; Edwin H Cook; Vladimir Coric; Bernadette A Cullen; Dieter Deforce; Richard Delorme; Yves Dion; Christopher K Edlund; Karin Egberts; Peter Falkai; Thomas V Fernandez; Patience J Gallagher; Helena Garrido; Daniel Geller; Simon L Girard; Hans J Grabe; Marco A Grados; Benjamin D Greenberg; Varda Gross-Tsur; Stephen Haddad; Gary A Heiman; Sian M J Hemmings; Ana G Hounie; Cornelia Illmann; Joseph Jankovic; Michael A Jenike; James L Kennedy; Robert A King; Barbara Kremeyer; Roger Kurlan; Nuria Lanzagorta; Marion Leboyer; James F Leckman; Leonhard Lennertz; Chunyu Liu; Christine Lochner; Thomas L Lowe; Fabio Macciardi; James T McCracken; Lauren M McGrath; Sandra C Mesa Restrepo; Rainald Moessner; Jubel Morgan; Heike Muller; Dennis L Murphy; Allan L Naarden; William Cornejo Ochoa; Roel A Ophoff; Lisa Osiecki; Andrew J Pakstis; Michele T Pato; Carlos N Pato; John Piacentini; Christopher Pittenger; Yehuda Pollak; Scott L Rauch; Tobias J Renner; Victor I Reus; Margaret A Richter; Mark A Riddle; Mary M Robertson; Roxana Romero; Maria C Rosàrio; David Rosenberg; Guy A Rouleau; Stephan Ruhrmann; Andres Ruiz-Linares; Aline S Sampaio; Jack Samuels; Paul Sandor; Brooke Sheppard; Harvey S Singer; Jan H Smit; Dan J Stein; E Strengman; Jay A Tischfield; Ana V Valencia Duarte; Homero Vallada; Filip Van Nieuwerburgh; Jeremy Veenstra-Vanderweele; Susanne Walitza; Ying Wang; Jens R Wendland; Herman G M Westenberg; Yin Yao Shugart; Euripedes C Miguel; William McMahon; Michael Wagner; Humberto Nicolini; Danielle Posthuma; Gregory L Hanna; Peter Heutink; Damiaan Denys; Paul D Arnold; Ben A Oostra; Gerald Nestadt; Nelson B Freimer; David L Pauls; Naomi R Wray; S Evelyn Stewart; Carol A Mathews; James A Knowles; Nancy J Cox; Jeremiah M Scharf
Journal:  PLoS Genet       Date:  2013-10-24       Impact factor: 5.917

View more
  5 in total

1.  Mechanisms of Action of Semen Ziziphi spinosae in the Treatment of Tourette Syndrome.

Authors:  Fei Fan; Fei Han; Long Hao
Journal:  Degener Neurol Neuromuscul Dis       Date:  2022-07-15

2.  EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder.

Authors:  Mathis Hildonen; Amanda M Levy; Christine Søholm Hansen; Jonas Bybjerg-Grauholm; Axel Skytthe; Nanette M Debes; Qihua Tan; Zeynep Tümer
Journal:  Genes (Basel)       Date:  2021-09-26       Impact factor: 4.096

3.  A Pilot Study on Plasma and Urine Neurotransmitter Levels in Children with Tic Disorders.

Authors:  Qiao-Qiao Qian; Qian-Qian Tan; Dan Sun; Qing Lu; Ying-Ying Xin; Qian Wu; Yong Zhou; Yang-Xi Liu; Pei-Chao Tian; Zhi-Sheng Liu
Journal:  Brain Sci       Date:  2022-07-04

Review 4.  Current understanding of the genetics of tourette syndrome.

Authors:  Wei-De Lin; Fuu-Jen Tsai; I-Ching Chou
Journal:  Biomed J       Date:  2022-01-15       Impact factor: 7.892

Review 5.  Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome-Where Are We?

Authors:  Amanda M Levy; Peristera Paschou; Zeynep Tümer
Journal:  Genes (Basel)       Date:  2021-08-26       Impact factor: 4.096

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.