Skip to main content
Log in

Identification of candidate genes of autism on the basis of molecular cytogenetic and in silico studies of the genome organization of chromosomal regions involved in unbalanced rearrangements

  • Published:
Russian Journal of Genetics Aims and scope Submit manuscript

Abstract

Autism is one of the most widely spread mental diseases among children. Different genetic anomalies make a considerable contribution to the etiology of this disease; therefore, the identification of candidate genes of autism can be regarded as a topical task of modern medical genetics. The molecular cytogenetic examination of children with autism was carried out using high-resolution comparative genome hybridization and subsequent in silico analysis of chromosomal regions involved in unbalanced rearrangements. Five of 126 (4%) children with autism had unbalanced rearrangements of chromosomes 5, 17, 21 (deletions) and chromosomes 4 and 22 (duplications). The following candidate genes were identified in children with autism by in silico analysis: SCARB2, TPPP, PDCD6, SEPT5, GP1BB, PI4KA, NPTX1, STCH, NRIP1, and CXADR. These methods also allowed us to find a possible association between gene clusterization and the formation of the described chromosomal rearrangements. Thus, this study demonstrates that the molecular cytogenetic and bioinformatic methods can be successfully used to search for candidate genes of different diseases and analyze the genome organization.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. Iourov, I.Yu., Vorsanova, S.G., and Yurov, Yu.B., Chromosomal Variation in Mammalian Neuronal Cells: Known Facts and Attractive Hypotheses, Int. Rev. Cytol., 2006, vol. 249, pp. 143–191.

    Article  PubMed  CAS  Google Scholar 

  2. Iourov, I.Yu., Vorsanova, S.G., and Yurov, Yu.B., Intercellular Genomic (Chromosomal) Variations Resulting in Somatic Mosaicism: Mechanisms and Consequences, Curr. Genomics, 2006, vol. 7, no. 7, pp. 435–446.

    Article  CAS  Google Scholar 

  3. Iourov, I.Yu., Vorsanova, S.G., and Yurov, Yu.B., Molecular Cytogenetics and Cytogenomics of Brain Diseases, Curr. Genomics, 2008, vol. 9, no. 7, pp. 452–465.

    Article  PubMed  CAS  Google Scholar 

  4. Vorsanova, S.G., Yurov, I.Yu., Soloviev, I.V., and Yurov, Yu.B., Geterokhromatinovye raiony khromosom cheloveka: kliniko-biologicheskie aspekty (Heterochromatic Regions of Human Chromosomes: Clinicobiological Aspects), Moscow: Medpraktika, 2008.

    Google Scholar 

  5. Soloviev, I.V., Yurov, Yu.B., Vorsanova, S.G., et al., Prenatal Diagnosis of Trisomy 21 Using Interphase Fluorescence in situ Hybridization of Post-Replicated Cells with Site-Specific Cosmid and Cosmid Contig Probes, Prenatal Diagn., vol. 15, no. 3, pp. 237–248.

  6. Vorsanova, S.G., Kolotii, A.D., Iourov, I.Yu., et al., Evidence for High Frequency of Chromosomal Mosaicism in Spontaneous Abortions Revealed by Interphase FISH Analysis, J. Histochem. Cytochem., 2005, vol. 53, no. 3, pp. 375–380.

    Article  PubMed  CAS  Google Scholar 

  7. Yurov, Yu.B., Iourov, I.Yu., Monakhov, V.V., et al., The Variation of Aneuploidy Frequency in the Developing and Adult Human Brain Revealed by an Interphase FISH Study, J. Histochem. Cytochem., 2005, vol. 53, no. 3, pp. 385–390.

    Article  PubMed  CAS  Google Scholar 

  8. Iourov, I.Yu., Soloviev, I.V., Vorsanova, S.G., et al., An Approach for Quantitative Assessment of Fluorescence in situ Hybridization (FISH) Signals for Applied Human Molecular Cytogenetics, J. Histochem. Cytochem., 2005, vol. 53, no. 3, pp. 401–408.

    Article  PubMed  CAS  Google Scholar 

  9. Iourov, I.Yu., Liehr, T., Vorsanova, S.G., et al., Visualization of Interphase Chromosomes in Postmitotic Cells of the Human Brain by Multicolour Banding (MCB), Chromosome Res., 2006, vol. 14, no. 3, pp. 223–229.

    Article  PubMed  CAS  Google Scholar 

  10. Iourov, I.Yu., Liehr, T., Vorsanova, S.G., and Yurov, Yu.B., Interphase Chromosome-Specific Multicolor Banding (ICS-MCB): A New Tool for Analysis of Interphase Chromosomes in Their Integrity, Biomol. Eng., 2007, vol. 24, no. 4, pp. 415–417.

    Article  PubMed  CAS  Google Scholar 

  11. Yurov, Yu.B., Iourov, I.Yu., Vorsanova, S.G., et al., Aneuploidy and Confined Chromosomal Mosaicism in the Developing Human Brain, PLoS ONE, 2007, vol. 2, no. 6, p. e558.

    Article  PubMed  CAS  Google Scholar 

  12. Iourov, I.Yu., Vorsanova, S.G., Liehr, T., and Yurov, Yu.B., Aneuploidy in the Normal, Alzheimer’s Disease and Ataxia-Telangiectasia Brain: Differential Expression and Pathological Meaning, Neurobiol. Dis., 2009, vol. 34, no. 2, pp. 212–220.

    Article  PubMed  CAS  Google Scholar 

  13. Yurov, I.Yu., Vorsanova, S.G., Kolotii, A.D., et al., Mosaic Aneuploidy in Ataxia-Telangiectasia (Syndrome Lui-Bar) Brain Cells, Med. Genetika, 2008, vol. 7, no. 7, pp. 22–26.

    Google Scholar 

  14. Iourov, I.Yu., Vorsanova, S.G., Liehr, T., et al., Increased Chromosome Instability Dramatically Disrupts Neural Genome Integrity and Mediates Cerebellar Degeneration in the Ataxia-Telangiectasia Brain, Hum. Mol. Genet., 2009, vol. 18, no. 14, pp. 2656–2669.

    Article  PubMed  CAS  Google Scholar 

  15. Yurov, Yu.B., Vostrikov, V.M., Vorsanova, S.G., et al., Multicolor Fluorescent in situ Hybridization on Post-Mortem Brain in Schizophrenia as an Approach for Identification of Low-Level Chromosomal Aneuploidy in Neuropsychiatric Diseases, Brain Dev., 2001, vol. 23, no. S1, pp. 186–190.

    Article  Google Scholar 

  16. Yurov, Yu.B., Iourov, I.Yu., Vorsanova, S.G., et al., The Schizophrenia Brain Exhibits Low-Level Aneuploidy Involving Chromosome 1, Schizophr. Res., 2008, vol. 98, nos. 1–3, pp. 137–147.

    Google Scholar 

  17. Vorsanova, S.G., Yurov (Iourov), I.Yu., Demidova, I.A., et al., Variability in the Heterochromatin Regions of the Chromosomes and Chromosomal Anomalies in Children with Autism: Identification of Genetic Markers of Autistic Spectrum Disorders, Neurosci. Behav. Physiol., 2007, vol. 37, no. 6, pp. 553–558.

    Article  PubMed  CAS  Google Scholar 

  18. Yurov, Yu.B., Vorsanova, S.G., Iourov, I.Yu., et al., Unexplained Autism Is Frequently Associated with Low-Level Mosaic Aneuploidy, J. Med. Genet., 2007, vol. 44, no. 8, pp. 521–525.

    Article  PubMed  CAS  Google Scholar 

  19. Vorsanova, S.G., Voinova, V.Yu., Iourov, I.Yu., et al., Cytogenetic, Molecular-Cytogenetic and Clinico-Genealogical Investigation of Mothers Having Children with Autism: A Search for Familial Genetic Markers of Autistic Disorders, Zh. Nevrol. Psikhiatr., 2009, vol. 109, no. 6, pp. 54–64.

    CAS  Google Scholar 

  20. Iourov, I.Yu., Vorsanova, S.G., and Yurov, Yu.B., Chromosomal Mosaicism Goes Global, Mol. Cytogenet., 2008, vol. 1, p. 26.

    Article  PubMed  CAS  Google Scholar 

  21. Yurov, Yu.B., Vorsanova, S.G., and Iourov, I.Yu., GIN’n’CIN Hypothesis of Brain Aging: Deciphering the Role of Somatic Genetic Instabilities and Neural Aneuploidy during Ontogeny, Mol. Cytogenet., 2009, vol. 2, p. 23.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to I. Yu. Iourov.

Additional information

Original Russian Text © I.Yu. Iourov, S.G. Vorsanova, E.A. Saprina, Yu.B. Yurov, 2010, published in Genetika, 2010, Vol. 46, No. 10, pp. 1348–1351.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Iourov, I.Y., Vorsanova, S.G., Saprina, E.A. et al. Identification of candidate genes of autism on the basis of molecular cytogenetic and in silico studies of the genome organization of chromosomal regions involved in unbalanced rearrangements. Russ J Genet 46, 1190–1193 (2010). https://doi.org/10.1134/S102279541010011X

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S102279541010011X

Keywords

Navigation