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No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population

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The RTN4R gene is located in the 22q11 region and it encodes a subunit of the receptor complex (RTN4R-p75NTR) which results in neuronal growth inhibitory signals in response to Nogo-66, MAG or OMG signaling. Previous studies have suggested that RTN4R might act as a potential candidate for schizophrenia susceptibility loci. We genotyped four SNPs within the gene and conducted a case-control study and TDT analysis, involving 707 schizophrenic patients, 689 controls and 372 unrelated small nuclear families with schizophrenic offspring in the Chinese population. We examined allele and genotype frequencies and haplotype distributions in both family- and nonfamily-based samples. Our results suggest that there is no significant association between the genetic polymorphisms and schizophrenia in the Han Chinese population.

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References

  • M Baron (2001) ArticleTitleGenetics of schizophrenia and the new millennium: progress and pitfalls Am J Hum Genet 68 299–312 Occurrence Handle11170887 Occurrence Handle10.1086/318212 Occurrence Handle1:CAS:528:DC%2BD3MXhtl2ls7k%3D

    Article  PubMed  CAS  Google Scholar 

  • TD Cannon J Kaprio J Lonnqvist M Huttunen M Koskenvuo (1998) ArticleTitleThe genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study Arch Gen Psychiatry 55 67–74 Occurrence Handle9435762 Occurrence Handle10.1001/archpsyc.55.1.67 Occurrence Handle1:STN:280:DyaK1c%2FpvVSmsw%3D%3D

    Article  PubMed  CAS  Google Scholar 

  • AG Cardno EJ Marshall B Coid AM Macdonald TR Ribchester NJ Davies P Venturi LA Jones SW Lewis PC Sham II Gottesman AE Farmer P McGuffin AM Reveley RM Murray (1999) ArticleTitleHeritability estimates for psychotic disorders: the Maudsley twin psychosis series Arch Gen Psychiatry 56 162–168 Occurrence Handle10025441 Occurrence Handle10.1001/archpsyc.56.2.162 Occurrence Handle1:STN:280:DyaK1M7kvVejug%3D%3D

    Article  PubMed  CAS  Google Scholar 

  • LR Cardon LJ Palmer (2003) ArticleTitlePopulation stratification and spurious allelic association Lancet 361 598–604 Occurrence Handle12598158 Occurrence Handle10.1016/S0140-6736(03)12520-2

    Article  PubMed  Google Scholar 

  • W Chen N Gu S Duan Y Sun Y Zheng C Li Y Pan Y Xu G Feng L He (2004a) ArticleTitleNo association between the genetic polymorphisms within RTN4 and schizophrenia in the Chinese population Neurosci Lett 365 23–27 Occurrence Handle10.1016/j.neulet.2004.04.021 Occurrence Handle1:CAS:528:DC%2BD2cXltl2hu7c%3D

    Article  CAS  Google Scholar 

  • WY Chen YY Shi YL Zheng XZ Zhao GJ Zhang SQ Chen PD Yang L He (2004b) ArticleTitleCase-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8 Hum Mol Genet 13 2991–2995 Occurrence Handle10.1093/hmg/ddh322 Occurrence Handle1:CAS:528:DC%2BD2cXhtVSkt7fI

    Article  CAS  Google Scholar 

  • HM Colhoun PM McKeigue G Davey Smith (2003) ArticleTitleProblems of reporting genetic associations with complex outcomes Lancet 361 865–872 Occurrence Handle12642066 Occurrence Handle10.1016/S0140-6736(03)12715-8

    Article  PubMed  Google Scholar 

  • KL Davis DG Stewart JI Friedman M Buchsbaum PD Harvey PR Hof J Buxbaum V Haroutunian (2003) ArticleTitleWhite matter changes in schizophrenia: evidence for myelin-related dysfunction Arch Gen Psychiatry 60 443–456 Occurrence Handle12742865 Occurrence Handle10.1001/archpsyc.60.5.443

    Article  PubMed  Google Scholar 

  • A De Luca A Pasini F Amati A Botta G Spalletta S Alimenti F Caccamo E Conti J Trakalo F Macciardi B Dallapiccola G Novelli (2001) ArticleTitleAssociation study of a promoter polymorphism of UFD1L gene with schizophrenia Am J Med Genet 105 529–533 Occurrence Handle11496370 Occurrence Handle10.1002/ajmg.1489 Occurrence Handle1:STN:280:DC%2BD3MvltVWjtw%3D%3D

    Article  PubMed  CAS  Google Scholar 

  • A De Luca E Conti N Grifone F Amati G Spalletta C Caltagirone G Bonaviri A Pasini M Gennarelli B Stefano L Berti G Mittler M Meisterernst B Dallapiccola G Novelli (2003) ArticleTitleAssociation study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia Am J Med Genet B Neuropsychiatr Genet 116 32–35 Occurrence Handle12497610 Occurrence Handle10.1002/ajmg.b.10008

    Article  PubMed  Google Scholar 

  • M Domeniconi Z Cao T Spencer R Sivasankaran K Wang E Nikulina N Kimura H Cai K Deng Y Gao Z He M Filbin (2002) ArticleTitleMyelin-associated glycoprotein interacts with the Nogo66 receptor to inhibit neurite outgrowth Neuron 35 283–290 Occurrence Handle12160746 Occurrence Handle10.1016/S0896-6273(02)00770-5 Occurrence Handle1:CAS:528:DC%2BD38XlvVCmu7o%3D

    Article  PubMed  CAS  Google Scholar 

  • S Dracheva KL Davis B Chin DA Woo J Schmeidler V Haroutunian (2006) ArticleTitleMyelin-associated mRNA and protein expression deficits in the anterior cingulate cortex and hippocampus in elderly schizophrenia patients Neurobiol Dis 21 531–540 Occurrence Handle16213148 Occurrence Handle10.1016/j.nbd.2005.08.012 Occurrence Handle1:CAS:528:DC%2BD28Xhslyhsbc%3D

    Article  PubMed  CAS  Google Scholar 

  • AE Fournier T GrandPre SM Strittmatter (2001) ArticleTitleIdentification of a receptor mediating Nogo-66 inhibition of axonal regeneration Nature 409 341–346 Occurrence Handle11201742 Occurrence Handle10.1038/35053072 Occurrence Handle1:CAS:528:DC%2BD3MXms12lsg%3D%3D

    Article  PubMed  CAS  Google Scholar 

  • Y Hakak JR Walker C Li WH Wong KL Davis JD Buxbaum V Haroutunian AA Fienberg (2001) ArticleTitleGenome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia Proc Natl Acad Sci USA 98 4746–4751 Occurrence Handle11296301 Occurrence Handle10.1073/pnas.081071198 Occurrence Handle1:CAS:528:DC%2BD3MXjtVant7w%3D

    Article  PubMed  CAS  Google Scholar 

  • ML Hamshere P Bennett N Williams R Segurado A Cardno N Norton D Lambert H Williams G Kirov A Corvin P Holmans L Jones I Jones M Gill MC O’Donovan MJ Owen N Craddock (2005) ArticleTitleGenomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19q13 Arch Gen Psychiatry 62 1081–1088 Occurrence Handle16203953 Occurrence Handle10.1001/archpsyc.62.10.1081 Occurrence Handle1:CAS:528:DC%2BD2MXhtFOgs77N

    Article  PubMed  CAS  Google Scholar 

  • PJ Harrison MJ Owen (2003) ArticleTitleGenes for schizophrenia? Recent findings and their pathophysiological implications Lancet 361 417–419 Occurrence Handle12573388 Occurrence Handle10.1016/S0140-6736(03)12379-3 Occurrence Handle1:CAS:528:DC%2BD3sXptFeisw%3D%3D

    Article  PubMed  CAS  Google Scholar 

  • HE Hulshoff Pol HG Schnack RC Mandl NE van Haren H Koning DL Collins AC Evans RS Kahn (2001) ArticleTitleFocal gray matter density changes in schizophrenia Arch Gen Psychiatry 58 1118–1125 Occurrence Handle11735840 Occurrence Handle10.1001/archpsyc.58.12.1118 Occurrence Handle1:STN:280:DC%2BD38%2FivVyltQ%3D%3D

    Article  PubMed  CAS  Google Scholar 

  • J Lappalainen HR Kranzler I Petrakis LK Somberg G Page JH Krystal J Gelernter (2004) ArticleTitleConfirmation and fine mapping of the chromosome 1 alcohol dependence risk locus Mol Psychiatry 9 312–319 Occurrence Handle15094791 Occurrence Handle10.1038/sj.mp.4001429 Occurrence Handle1:CAS:528:DC%2BD2cXhvFCmsLc%3D

    Article  PubMed  CAS  Google Scholar 

  • DA Lewis P Levitt (2002) ArticleTitleSchizophrenia as a disorder of neurodevelopment Annu Rev Neurosci 25 409–432 Occurrence Handle12052915 Occurrence Handle10.1146/annurev.neuro.25.112701.142754 Occurrence Handle1:CAS:528:DC%2BD38XmtF2hsbw%3D

    Article  PubMed  CAS  Google Scholar 

  • H Liu GR Abecasis SC Heath A Knowles S Demars YJ Chen JL Roos JL Rapoport JA Gogos M Karayiorgou (2002a) ArticleTitleGenetic variation in the 22q11 locus and susceptibility to schizophrenia Proc Natl Acad Sci USA 99 16859–16864 Occurrence Handle10.1073/pnas.232186099 Occurrence Handle1:CAS:528:DC%2BD3sXhvV2gug%3D%3D

    Article  CAS  Google Scholar 

  • H Liu SC Heath C Sobin JL Roos BL Galke ML Blundell M Lenane B Robertson EM Wijsman JL Rapoport JA Gogos M Karayiorgou (2002b) ArticleTitleGenetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia Proc Natl Acad Sci USA 99 3717–3722 Occurrence Handle10.1073/pnas.042700699 Occurrence Handle1:CAS:528:DC%2BD38Xis1Kltro%3D

    Article  CAS  Google Scholar 

  • CE Ng BL Tang (2002) ArticleTitleNogos and the Nogo-66 receptor: factors inhibiting CNS neuron regeneration J Neurosci Res 67 559–565 Occurrence Handle11891768 Occurrence Handle10.1002/jnr.10134 Occurrence Handle1:CAS:528:DC%2BD38XisVKnsLg%3D

    Article  PubMed  CAS  Google Scholar 

  • MJ Owen NM Williams MC O’Donovan (2004) ArticleTitleThe molecular genetics of schizophrenia: new findings promise new insights Mol Psychiatry 9 14–27 Occurrence Handle14581932 Occurrence Handle10.1038/sj.mp.4001444 Occurrence Handle1:CAS:528:DC%2BD3sXhtVWhtr7F

    Article  PubMed  CAS  Google Scholar 

  • S Purcell SS Cherny PC Sham (2003) ArticleTitleGenetic Power Calculator: design of linkage and association genetic mapping studies of complex traits Bioinformatics 19 149–150 Occurrence Handle12499305 Occurrence Handle10.1093/bioinformatics/19.1.149 Occurrence Handle1:CAS:528:DC%2BD3sXltF2ksQ%3D%3D

    Article  PubMed  CAS  Google Scholar 

  • HK Sandhu N Hollenbeck TH Wassink RA Philibert (2004) ArticleTitleAn association study of PCQAP polymorphisms and schizophrenia Psychiatr Genet 14 169–172 Occurrence Handle15318033 Occurrence Handle10.1097/00041444-200409000-00010

    Article  PubMed  Google Scholar 

  • PC Sham D Curtis (1995) ArticleTitleMonte Carlo tests for associations between disease and alleles at highly polymorphic loci Ann Hum Genet 59 97–105 Occurrence Handle7762987 Occurrence Handle1:STN:280:ByqB1czisVQ%3D

    PubMed  CAS  Google Scholar 

  • YY Shi L He (2005) ArticleTitleSHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci Cell Res 15 97–98 Occurrence Handle15740637 Occurrence Handle10.1038/sj.cr.7290286 Occurrence Handle1:CAS:528:DC%2BD2MXksFynsro%3D

    Article  PubMed  CAS  Google Scholar 

  • S Shifman M Bronstein M Sternfeld A Pisante-Shalom E Lev-Lehman A Weizman I Reznik B Spivak N Grisaru L Karp R Schiffer M Kotler RD Strous M Swartz-Vanetik HY Knobler E Shinar JS Beckmann B Yakir N Risch NB Zak A Darvasi (2002) ArticleTitleA highly significant association between a COMT haplotype and schizophrenia Am J Hum Genet 71 1296–1302 Occurrence Handle12402217 Occurrence Handle10.1086/344514 Occurrence Handle1:CAS:528:DC%2BD3sXjsV2m

    Article  PubMed  CAS  Google Scholar 

  • L Sinibaldi A De Luca E Bellacchio E Conti A Pasini C Paloscia G Spalletta C Caltagirone A Pizzuti B Dallapiccola (2004) ArticleTitleMutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia Hum Mutat 24 534–535 Occurrence Handle15532024 Occurrence Handle10.1002/humu.9292

    Article  PubMed  Google Scholar 

  • D Tkachev ML Mimmack MM Ryan M Wayland T Freeman PB Jones M Starkey MJ Webster RH Yolken S Bahn (2003) ArticleTitleOligodendrocyte dysfunction in schizophrenia and bipolar disorder Lancet 362 798–805 Occurrence Handle13678875 Occurrence Handle10.1016/S0140-6736(03)14289-4 Occurrence Handle1:CAS:528:DC%2BD3sXntVGktLc%3D

    Article  PubMed  CAS  Google Scholar 

  • EJ van den Oord BM Neale (2004) ArticleTitleWill haplotype maps be useful for finding genes? Mol Psychiatry 9 227–236 Occurrence Handle14610524 Occurrence Handle10.1038/sj.mp.4001449 Occurrence Handle1:CAS:528:DC%2BD2cXhvFCmsb0%3D

    Article  PubMed  CAS  Google Scholar 

  • JD Wall JK Pritchard (2003) ArticleTitleHaplotype blocks and linkage disequilibrium in the human genome Nat Rev Genet 4 587–597 Occurrence Handle12897771 Occurrence Handle10.1038/nrg1123 Occurrence Handle1:CAS:528:DC%2BD3sXlvFaqtrc%3D

    Article  PubMed  CAS  Google Scholar 

  • KC Wang V Koprivica JA Kim R Sivasankaran Y Guo RL Neve Z He (2002) ArticleTitleOligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth Nature 417 941–944 Occurrence Handle12068310 Occurrence Handle10.1038/nature00867 Occurrence Handle1:CAS:528:DC%2BD38XkvVagsbc%3D

    Article  PubMed  CAS  Google Scholar 

  • ST Wong JR Henley KC Kanning KH Huang M Bothwell MM Poo (2002) ArticleTitleA p75(NTR) and Nogo receptor complex mediates repulsive signaling by myelin-associated glycoprotein Nat Neurosci 5 1302–1308 Occurrence Handle12426574 Occurrence Handle10.1038/nn975 Occurrence Handle1:CAS:528:DC%2BD38XovFChs7k%3D

    Article  PubMed  CAS  Google Scholar 

  • YF Yang W Qin YY Shugart G He XM Liu J Zhou XZ Zhao Q Chen YJ La YF Xu XW Li NF Gu GY Feng H Song P Wang L He (2005) ArticleTitlePossible association of the MAG locus with schizophrenia in a Chinese Han cohort of family trios Schizophr Res 75 11–19 Occurrence Handle15820319 Occurrence Handle10.1016/j.schres.2004.11.013 Occurrence Handle1:STN:280:DC%2BD2M3jvVWjsg%3D%3D

    Article  PubMed  CAS  Google Scholar 

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Meng, J., Shi, Y., Zhao, X. et al. No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population. J Neural Transm 114, 249–254 (2007). https://doi.org/10.1007/s00702-006-0538-y

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