Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
- PMID: 11741194
- PMCID: PMC384904
- DOI: 10.1086/338241
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
Abstract
Autism is a syndrome characterized by deficits in language and social skills and by repetitive behaviors. We hypothesized that potential quantitative trait loci (QTLs) related to component autism endophenotypes might underlie putative or significant regions of autism linkage. We performed nonparametric multipoint linkage analyses, in 152 families from the Autism Genetic Resource Exchange, focusing on three traits derived from the Autism Diagnostic Interview: "age at first word," "age at first phrase," and a composite measure of "repetitive and stereotyped behavior." Families were genotyped for 335 markers, and multipoint sib pair linkage analyses were conducted. Using nonparametric multipoint linkage analysis, we found the strongest QTL evidence for age at first word on chromosome 7q (nonparametric test statistic [Z] 2.98; P=.001), and subsequent linkage analyses of additional markers and association analyses in the same region supported the initial result (Z=2.85, P=.002; chi(2)=18.84, df 8, P=.016). Moreover, the peak fine-mapping result for repetitive behavior (Z=2.48; P=.007) localized to a region overlapping this language QTL. The putative autism-susceptibility locus on chromosome 7 may be the result of separate QTLs for the language and repetitive or stereotyped behavior deficits that are associated with the disorder.
Figures





























Similar articles
-
Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.Mol Psychiatry. 2005 Aug;10(8):747-57. doi: 10.1038/sj.mp.4001666. Mol Psychiatry. 2005. PMID: 15824743
-
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.BMC Med Genet. 2005 Jan 12;6:1. doi: 10.1186/1471-2350-6-1. BMC Med Genet. 2005. PMID: 15647115 Free PMC article.
-
A quantitative trait locus analysis of social responsiveness in multiplex autism families.Am J Psychiatry. 2007 Apr;164(4):656-62. doi: 10.1176/ajp.2007.164.4.656. Am J Psychiatry. 2007. PMID: 17403980
-
The molecular genetics of autism.Curr Psychiatry Rep. 2000 Apr;2(2):170-5. doi: 10.1007/s11920-000-0063-x. Curr Psychiatry Rep. 2000. PMID: 11122951 Review.
-
The genetics of autism.Pediatrics. 2004 May;113(5):e472-86. doi: 10.1542/peds.113.5.e472. Pediatrics. 2004. PMID: 15121991 Review.
Cited by
-
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.Hum Genet. 2016 Dec;135(12):1329-1341. doi: 10.1007/s00439-016-1717-z. Epub 2016 Aug 17. Hum Genet. 2016. PMID: 27535846 Free PMC article.
-
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders.Hum Genet. 2012 Nov;131(11):1687-98. doi: 10.1007/s00439-012-1193-z. Epub 2012 Jun 27. Hum Genet. 2012. PMID: 22736078 Free PMC article. Review.
-
Language characterization in 16p11.2 deletion and duplication syndromes.Am J Med Genet B Neuropsychiatr Genet. 2020 Sep;183(6):380-391. doi: 10.1002/ajmg.b.32809. Epub 2020 Jul 11. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 32652891 Free PMC article.
-
A genomewide screen of 345 families for autism-susceptibility loci.Am J Hum Genet. 2003 Oct;73(4):886-97. doi: 10.1086/378778. Epub 2003 Sep 17. Am J Hum Genet. 2003. PMID: 13680528 Free PMC article.
-
Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.Biol Psychiatry. 2008 Oct 1;64(7):561-70. doi: 10.1016/j.biopsych.2008.05.023. Epub 2008 Jul 16. Biol Psychiatry. 2008. PMID: 18632090 Free PMC article.
References
Electronic-Database Information
-
- AGRE, http://agre.org/
-
- Center for Medical Genetics, Marshfield Medical Research Foundation, http://research.marshfieldclinic.org/genetics/
-
- Genome Database, The, http://gdbwww.gdb.org/
-
- Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/ (for autism disorder [MIM accession number 209850])
References
-
- Aita VM, Christiano AM, Gilliam TC (1999) Mapping complex traits in diseases of the hair and skin. Exp Dermatol 8:439–452 - PubMed
-
- Alarcón M, Cantor RM (2001) QTL mapping of serum IgE in an isolated Hutterite population. Genet Epidemiol 21:S224–S229 - PubMed
-
- Anderson MA, Gusella JF (1984) Use of cyclosporin A in establishing Epstein-Barr virus–transformed human lymphoblastoid cell lines. In Vitro 20:856–858 - PubMed
-
- Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Aylsworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA (1999) Genetic studies of autistic disorder and chromosome 7. Genomics 61:227–236 - PubMed
-
- Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, Rutter M (1995) Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med 25:63–77 - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous