Association of RANBP1 haplotype with smooth pursuit eye movement abnormality

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 156, Issue 1, 2011, Pages 67-71

  Cheong, Hyun Sub ^a   Park, Byung Lae ^a   Kim, Eun Mi ^a   Park, Chul Soo ^b   Sohn, Jin Wook ^b   Kim, Bong Jo ^b   Kim, Jae Won ^c   Kim, Ki Hoon ^d   Shin, Tae Min ^d   Choi, Ihn Geun ^e   Han, Sang Woo ^f   Hwang, Jaeuk ^f   Koh, Insong ^g   Shin, Hyoung Doo ^a,h   Woo, Sung Il ^f  

^a SNP Genetics Inc   (South Korea)

^b Gyeongsang National University School of Medicine   (South Korea)

^c Gyeongsang National University   (South Korea)

^d Yonsei University Wonju   (South Korea)

^e Hallym University   (South Korea)

^f Soonchunhyang University College of Medicine   (South Korea)

^g Hanyang University   (South Korea)

^h Sogang University   (South Korea)

Author keywords

RANBP1; Schizophrenia; Single nucleotide polymorphism; Smooth pursuit eye movement

Indexed keywords

BINDING PROTEIN; NUCLEAR PROTEIN; RAN BINDING PROTEIN 1; UNCLASSIFIED DRUG; RAN-BINDING PROTEIN 1;

ADULT; ARTICLE; CHROMOSOME 22Q; CONTROLLED STUDY; EYE MOVEMENT DISORDER; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HAPLOTYPE; HUMAN; INTRON; KOREA; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; SMOOTH PURSUIT EYE MOVEMENT DISTURBANCE; AGED; ASIAN; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; REGRESSION ANALYSIS; RISK FACTOR; SMOOTH PURSUIT EYE MOVEMENT; SOUTH KOREA;

ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; NUCLEAR PROTEINS; PURSUIT, SMOOTH; REGRESSION ANALYSIS; REPUBLIC OF KOREA; RISK FACTORS; SCHIZOPHRENIA; YOUNG ADULT;

EID: 79953667296     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.31139     Document Type: Article

References (24)

1. American Psychiatric Association. 1994. Diagnostic and statistical manual of mental disorders, 4th edition. Wasington, DC: American Psychiatric Association.
2. Badner JA, Gershon ES. 2002. Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 7(4): 405-411.
3. Barrett JC, Fry B, Maller J, Daly MJ. 2005. Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics 21(2): 263-265.
4. Bischoff FR, Krebber H, Smirnova E, Dong W, Ponstingl H. 1995. Co-activation of RanGTPase and inhibition of GTP dissociation by Ran-GTP binding protein RanBP1. EMBO J 14(4): 705-715.
5. Chi NC, Adam EJ, Visser GD, Adam SA. 1996. RanBP1 stabilizes the interaction of Ran with p97 nuclear protein import. J Cell Biol 135(3): 559-569.
6. Coman IL, Gnirke MH, Middleton FA, Antshel KM, Fremont W, Higgins AM, Shprintzen RJ, Kates WR. 2010. The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI study. Neuroimage 53(3): 1043-1050.
7. Hedrick PW. 1987. Gametic disequilibrium measures: Proceed with caution. Genetics 117(2): 331-341.
8. Holzman PS. 2000. Eye movements and the search for the essence of schizophrenia. Brain Res Brain Res Rev 31(2-3): 350-356.
9. Kehlenbach RH, Dickmanns A, Kehlenbach A, Guan T, Gerace L. 1999. A role for RanBP1 in the release of CRM1 from the nuclear pore complex in a terminal step of nuclear export. J Cell Biol 145(4): 645-657.
10. Kempf L, Nicodemus KK, Kolachana B, Vakkalanka R, Verchinski BA, Egan MF, Straub RE, Mattay VA, Callicott JH, Weinberger DR, et al. 2008. Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function. PLoS Genet 4(11): e1000252.
11. Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, et al. 2003. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. Am J Hum Genet 73(1): 34-48.
12. Liu H, Abecasis GR, Heath SC, Knowles A, Demars S, Chen YJ, Roos JL, Rapoport JL, Gogos JA, Karayiorgou M. 2002. Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci USA 99(26): 16859-16864.
13. Liu YL, Fann CS, Liu CM, Chang CC, Yang WC, Wu JY, Hung SI, Chan HY, Chen JJ, Hsieh MH, et al. 2007. HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention. Psychiatr Genet 17(6): 333-338.
14. Livak KJ. 1999. Allelic discrimination using fluorogenic probes and the 5′ nuclease assay. Genet Anal 14(5-6): 143-149.
15. McGrath J, Saha S, Welham J, El Saadi O, MacCauley C, Chant D. 2004. A systematic review of the incidence of schizophrenia: The distribution of rates and the influence of sex, urbanicity, migrant status and methodology. BMC Med 2: 13.
16. Meltzer HY, Brennan MD, Woodward ND, Jayathilake K. 2008. Association of Sult4A1 SNPs with psychopathology and cognition in patients with schizophrenia or schizoaffective disorder. Schizophr Res 106(2-3): 258-264.
17. Menashe I, Rosenberg PS, Chen BE. 2008. PGA: Power calculator for case-control genetic association analyses. BMC Genet 9: 36.
18. Mukai J, Liu H, Burt RA, Swor DE, Lai WS, Karayiorgou M, Gogos JA. 2004. Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia. Nat Genet 36(7): 725-731.
19. Murphy KC. 2002. Schizophrenia and velo-cardio-facial syndrome. Lancet 359(9304): 426-430.
20. Park BL, Shin HD, Cheong HS, Park CS, Sohn JW, Kim BJ, Seo HK, Kim JW, Kim KH, Shin TM, et al. 2009. Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality. J Hum Genet 54(12): 709-712.
21. Plafker K, Macara IG. 2002. Fluorescence resonance energy transfer biosensors that detect Ran conformational changes and a Ran x GDP-importin-beta -RanBP1 complex in vitro and in intact cells. J Biol Chem 277(33): 30121-30127.
22. Rybakowski JK, Borkowska A, Czerski PM, Hauser J. 2002. Eye movement disturbances in schizophrenia and a polymorphism of catechol-O-methyltransferase gene. Psychiatry Res 113(1-2): 49-57.
23. Shin HD, Park BL, Bae JS, Park TJ, Chun JY, Park CS, Sohn J-W, Kim B-J, Kang Y-H, Kim JW, et al. 2010. Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality. Neuropsychiatr Genet 153B(6): 1167-1172.
24. Vorstman JA, Turetsky BI, Sijmens-Morcus ME, de Sain MG, Dorland B, Sprong M, Rappaport EF, Beemer FA, Emanuel BS, Kahn RS, et al. 2009. Proline affects brain function in 22q11DS children with the low activity COMT 158 allele. Neuropsychopharmacology 34(3): 739-746.