Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 159 B, Issue 1, 2012, Pages 72-76

  Lei, Jing ^a   Deng, Xiong ^a   Zhang, Jie ^b   Su, Linyan ^c   Xu, Hongbo ^a   Liang, Hui ^a   Huang, Xian ^a   Song, Zhi ^a   Deng, Hao ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b HUNAN CHILDREN'S HOSPITAL   (China)

^c CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

Susceptibility; The HDC gene; Tourette syndrome; Variant

Indexed keywords

HISTIDINE DECARBOXYLASE;

ALLELE; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; ETHNICITY; EXON; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD;

ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHINA; DNA MUTATIONAL ANALYSIS; ETHNIC GROUPS; EXONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; HISTIDINE DECARBOXYLASE; HUMANS; INTRONS; MALE; OPEN READING FRAMES; TOURETTE SYNDROME;

EID: 83755172066     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32003     Document Type: Article

References (33)

1. American Psychiatric Association. 2000. Diagnostic and statistical manual of mental disorders, 4th edition-text revision (DSM-IV-TR). Washington, DC: American Psychiatric Press. p 111-114.
2. Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, Dure LS IV, Kurlan R, Singer HS, Gilbert DL, Farhi A, Louvi A, Lifton RP, Sestan N, State MW. 2005. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 310: 317-320.
3. Barr CL, Wigg KG, Zovko E, Sandor P, Tsui LC. 1997. Linkage study of the dopamine D5 receptor gene and Gilles de la tourette syndrome. Am J Med Genet (Neuropsychiatr Genet) 74: 58-61.
4. Belloso JM, Bache I, Guitart M, Caballin MR, Halgren C, Kirchhoff M, Ropers HH, Tommerup N, Tümer Z. 2007. Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome. Eur J Hum Genet 15: 711-713.
5. Brett PM, Curtis D, Robertson MM, Gurling HM. 1995. The genetic susceptibility to Gilles de la Tourette syndrome in a large multiple affected British kindred: Linkage analysis excludes a role for the genes coding for dopamine D1, D2, D3, D4, D5 receptors, dopamine beta hydroxylase, tyrosinase, and tyrosine hydroxylase. Biol psychiatry 37: 533-540.
6. Comings DE, Wu S, Chiu C, Ring RH, Gade R, Ahn C, MacMurray JP, Dietz G, Muhleman D. 1996. Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: The additive and subtractive effect of the three dopaminergic genes-DRD2, D beta H, and DAT1. Am J Med Genet (Neuropsychiatr Genet) 67: 364-388.
7. Dehning S, Müller N, Matz J, Bender A, Kerle I, Benninghoff J, Musil R, Spellmann I, Bondy B, Möller HJ, Riedel M, Zill P. 2010. A genetic variant of HTR2C may play a role in the manifestation of Tourette syndrome. Psychiatr Genet 20: 35-38.
8. Deng H, Le WD, Zhang X, Pan TH, Jankovic J. 2005. G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients. Acta Neurol Scand 111: 351-352.
9. Deng H, Le WD, Xie WJ, Jankovic J. 2006. Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome. Acta Neurol Scand 114: 400-402.
10. Deng H, Yang H, Le W, Deng X, Xu H, Zhu S, Xie W, Jankovic J. 2010. Examination of the MASH1 gene in patients with Parkinson's disease. Biochem Biophys Res Commun 392: 548-550.
11. Dere E, De Souza-Silva MA, Spieler RE, Lin JS, Ohtsu H, Haas HL, Huston JP. 2004. Changes in motoric, exploratory and emotional behaviours and neuronal acetylcholine content and 5-HT turnover in histidine decarboxylase-KO mice. Eur J Neurosci 20: 1051-1058.
12. Ercan-Sencick AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE, Abbott T, Gupta A, King RA, Pauls DL, Tischfield JA, Heiman GA, Singer HS, Gilbert DL, Hoekstra PJ, Morgan TM, Loring E, Yasuno K, Fernandez T, Sanders S, Louvi A, Cho JH, Mane S, Colangelo CM, Biederer T, Lifton RP, Gunel M, State MW. 2010. L-histidine decarboxylase and Tourette's syndrome. N Engl J Med 362: 1901-1908.
13. Freeman RD, Tourette Syndrome International Database Consortium. 2007. Tic disorders and ADHD: Answers from a world-wide clinical dataset on Tourette syndrome. Eur Child Adolesc Psychiatry 16: 536.
14. Guo Y, Deng X, Zheng W, Xu H, Song Z, Liang H, Lei J, Jiang X, Luo Z, Deng H. 2011. HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease. Neurosci Lett 501: 185-187.
15. Inoue I, Yanai K, Kitamura D, Taniuchi I, Kobayashi T, Niimura K, Watanabe T, Watanabe T. 1996. Impaired locomotor activity and exploratory behavior in mice lacking histamine H1 receptors. Proc Natl Acad Sci USA 93: 13316-13320.
16. Jeffries KJ, Schooler C, Schoenbach C, Herscovitch P, Chase TN, Braun AR. 2002. The functional neuroanatomy of Tourette's syndrome: An FDG PET study III: Functional coupling of regional cerebral metabolic rates. Neuropsychopharmacology 27: 92-104.
17. Jankovic J, Deng H. 2007. Candidate locus for chorea and tics disorders at 15q? Pediatr Neurol 37: 70-73.
18. Komar AA. 2007. Genetics. SNPs, silent but not invisible. Science 315: 466-467.
19. Kubota Y, Ito C, Sakurai E, Sakurai E, Watanabe T, Ohtsu H. 2002. Increased methamphetamine-induced locomotor activity and behavioral sensitization in histamine-deficient mice. J Neurochem 83: 837-845.
20. Lawson-Yuen A, Saldivar JS, Sommer S, Picker J. 2008. Familial deletion within NLGN4 associated with autism and Tourette syndrome. Eur J Hum Genet 16: 614-618.
21. Mérette C, Brassard A, Potvin A, Bouvier H, Rousseau F, Emond C, Bissonnette L, Roy MA, Maziade M, Ott J, Caron C. 2000. Significant linkage for Tourette syndrome in a large French Candian family. Am J Hum Genet 67: 1008-1013.
22. Ohtsu H, Watanabe T. 2003. New functions of histamine found in histidine decarboxylase gene knockout mice. Biochem Biophys Res Commun 305: 443-447.
23. Petek E, Windpassinger C, Vincent JB, Cheung J, Boright AP, Scherer SW, Kroisel PM, Wagner K. 2001. Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome. Am J Hum Genet 68: 848-858.
24. Price RA, Kidd KK, Cohen DJ, Pauls DL, Leckman JF. 1985. A twin study of Tourette syndrome. Arch Gen Psychiatry 42: 815-820.
25. Rivière JB, Xiong L, Levchenko A, St-Onge J, Gaspar C, Dion Y, Lespérance P, Tellier G, Richer F, Chouinard S, Rouleau GA, Montreal Tourette Study Group. 2009. Association of intronic variants of the BTBD9 gene with Tourette syndrome. Arch Neurol 66: 1267-1272.
26. Robertson MM, Eapen V, Cavanna AE. 2009. The international prevalence, epidemiology, and clinical phenomenology of Tourette syndrome: A cross-cultural perspective. J Psychosom Res 67: 475-483.
27. Sowell ER, Kan E, Yoshii J, Thompson PM, Bansal R, Xu D, Toga AW, Peterson BS. 2008. Thinning of sensorimotor cortices in children with Tourette syndrome. Nat Neurosci 11: 637-639.
28. Suzuki-Ishigaki S, Numayama-Tsuruta K, Kuramasu A, Sakurai E, Makabe Y, Shimura S, Shirato K, Igarashi K, Watanabe T, Ohtsu H. 2000. The mouse L-histidine decarboxylase gene: Structure and transcriptional regulation by CpG methylation in the promoter region. Nucleic Acids Res 28: 2627-2633.
29. Sundaram SK, Huq AM, Sun Z, Yu W, Bennett L, Wilson BJ, Behen ME, Chugani HT. 2011. Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder. Ann Neurol 69: 901-904.
30. Thi Tran HT, Takeshima Y, Surono A, Yagi M, Wada H, Matsuo M. 2005. A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro. Mol Genet Metab 85: 213-219.
31. Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA, Tourette Syndrome Association International Consortium for Genetics. 2003. CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics 82: 1-9.
32. Wang HS, Kuo MF. 2003. Tourette's syndrome in Taiwan: An epidemiological study of tic disorders in an elementary school at Taipei County. Brain Dev 25: 29-31.
33. Zimprich A, Hatala K, Riederer F, Stogmann E, Aschauer HN, Stamenkovic M. 2008. Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder. Psychiatr Genet 18: 308-309.