Dissecting the locus heterogeneity of autism

Significant linkage to chromosome 12q14

D. Q. Ma, Michael Cuccaro, J. M. Jaworski, C. S. Haynes, D. A. Stephan, J. Parod, R. K. Abramson, H. H. Wright, John Gilbert, J. L. Haines, Margaret A Pericak-Vance

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Autism is a common neurodevelopmental disorder with a significant genetic component and locus heterogeneity. To date, 12 microsatellite genome screens have been performed using various data sets of sib-pair families (parents and affected children) resulting in numerous regions of potential linkage across the genome. However, no universal region or consistent candidate gene from these regions has emerged. The use of large, extended pedigrees is a recognized powerful approach to identify significant linkage results, as these families potentially contain more potential linkage information than sib-pair families. A genome-wide linkage analysis was performed on 26 extended autism families (65 affected, 184 total individuals). Each family had two to four affected individuals comprised of either avuncular or cousin pairs. For analysis, we used a high-density single-nucleotide polymorphism genotyping assay, the Affymetrix GeneChip Human Mapping 10K array. Two-point analysis gave peak heterogeneity limit of detection (HLOD) of 2.82 at rs2877739 on chromosome 14q. Suggestive linkage evidence (HLOD>2) from a two-point analysis was also found on chromosomes 1q, 2q, 5q, 6p,11q and 12q. Chromosome 12q was the only region showing significant linkage evidence by multipoint analysis with a peak HLOD=3.02 at rs1445442. In addition, this linkage evidence was enhanced significantly in the families with only male affected (multipoint HLOD=4.51), suggesting a significant gender-specific effect in the etiology of autism. Chromosome-wide haplotype analyses on chromosome 12 localized the potential autism gene to a 4 cM region shared among the affected individuals across linked families. This novel linkage peak on chromosome 12q further supports the hypothesis of substantial locus heterogeneity in autism.

Original languageEnglish
Pages (from-to)376-384
Number of pages9
JournalMolecular Psychiatry
Volume12
Issue number4
DOIs
StatePublished - Apr 30 2007
Externally publishedYes

Fingerprint

Autistic Disorder
Chromosomes
Limit of Detection
Genome
Chromosomes, Human, Pair 12
Genetic Loci
Pedigree
Microsatellite Repeats
Haplotypes
Genes
Single Nucleotide Polymorphism
Parents

Keywords

  • Autism
  • Extended families
  • Genome screen
  • Single-nucleotide polymorphisms

ASJC Scopus subject areas

  • Molecular Biology
  • Psychiatry and Mental health

Cite this

Dissecting the locus heterogeneity of autism : Significant linkage to chromosome 12q14. / Ma, D. Q.; Cuccaro, Michael; Jaworski, J. M.; Haynes, C. S.; Stephan, D. A.; Parod, J.; Abramson, R. K.; Wright, H. H.; Gilbert, John; Haines, J. L.; Pericak-Vance, Margaret A.

In: Molecular Psychiatry, Vol. 12, No. 4, 30.04.2007, p. 376-384.

Research output: Contribution to journalArticle

Ma, DQ, Cuccaro, M, Jaworski, JM, Haynes, CS, Stephan, DA, Parod, J, Abramson, RK, Wright, HH, Gilbert, J, Haines, JL & Pericak-Vance, MA 2007, 'Dissecting the locus heterogeneity of autism: Significant linkage to chromosome 12q14', Molecular Psychiatry, vol. 12, no. 4, pp. 376-384. https://doi.org/10.1038/sj.mp.4001927
Ma, D. Q. ; Cuccaro, Michael ; Jaworski, J. M. ; Haynes, C. S. ; Stephan, D. A. ; Parod, J. ; Abramson, R. K. ; Wright, H. H. ; Gilbert, John ; Haines, J. L. ; Pericak-Vance, Margaret A. / Dissecting the locus heterogeneity of autism : Significant linkage to chromosome 12q14. In: Molecular Psychiatry. 2007 ; Vol. 12, No. 4. pp. 376-384.
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