Literature DB >> 26094621

Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism.

Jian Wang1,2,3, Yu Tao4, Fan Song4, Yue Sun1,2, Jurg Ott5, David Saffen1,2,4,6.   

Abstract

Based on the analysis of mRNA expression and genotype data from the "Brain Cloud" database, we identified seven SNPs within or near the autism candidate gene CYFIP1 that show nominally significant correlations between genotype and CYFIP1 mRNA expression in human dorsolateral prefrontal cortex. Analysis of transmission disequilibrium test (TDT) odds ratios (ORs) for these SNPs in a large Autism Genome Project (AGP) trio-based association study revealed the high-expression alleles of four of these SNPs (rs8028440, rs2289823, rs7403800 and rs3751566) to be susceptibility alleles. Correlations between the regression coefficients for mRNA expression and log10 -transformed TDT ORs were statistically significant [P = 0.008 (ASD); P = 0.002 (classical autism)]. Similarly, statistically significant correlations were obtained between levels of CYFIP1 mRNA expression predicted using the regression equations obtained from multiple linear regression analysis and log10 -transformed TDT ORs for specific combinations of genotypes for both ASD (rs2289823 + rs3751566: P = 0.008) and classical autism (rs2289823 + rs3751566: P = 0.008; rs2289823 + rs3751566 + rs765763: P = 0.0006) diagnoses. Together, these results support the hypothesis that high expression of CYFIP1 mRNA increases susceptibility for both ASD and classical autism.
© 2015 John Wiley & Sons Ltd/University College London.

Entities:  

Keywords:  CYFIP1; autism spectrum disorder; expression quantitative locus (eQTL); regulatory genetic variant

Year:  2015        PMID: 26094621     DOI: 10.1111/ahg.12121

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  20 in total

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2.  Cytoplasmic FMRP interacting protein 1/2 (CYFIP1/2) expression analysis in autism.

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4.  A Common CYFIP1 Variant at the 15q11.2 Disease Locus Is Associated with Structural Variation at the Language-Related Left Supramarginal Gyrus.

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6.  New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.

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7.  Autism As a Disorder of High Intelligence.

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8.  Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brain.

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Review 9.  Perturbed proteostasis in autism spectrum disorders.

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Review 10.  Modeling Fragile X Syndrome in Drosophila.

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Journal:  Front Mol Neurosci       Date:  2018-04-16       Impact factor: 5.639

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