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Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder.
Chien, Wei-Hsien; Chen, Chia-Hsiang; Cheng, Min-Chih; Wu, Yu-Yu; Gau, Susan Shur-Fen.
Afiliación
  • Chien WH; Department of Occupational Therapy, College of Medicine, Fu Jen Catholic University, New Taipei City 242062, Taiwan.
  • Chen CH; Department of Psychiatry, Linkou Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.
  • Cheng MC; Department of Psychiatry, Yuli Branch, Taipei Veterans General Hospital, Hualien 981, Taiwan.
  • Wu YY; Department of Psychiatry, Linkou Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.
  • Gau SS; Department of Psychiatry, National Taiwan University Hospital, Taipei 10002, Taiwan.
Int J Mol Sci ; 25(10)2024 May 19.
Article en En | MEDLINE | ID: mdl-38791584
ABSTRACT
Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with heterogeneous and complex genetic underpinnings. Our previous microarray gene expression profiling identified significantly different neuregulin-2 gene (NRG2) expression between ASD patients and controls. Thus, we aimed to clarify whether NRG2 is a candidate gene associated with ASD. The study consisted of two stages. First, we used real-time quantitative PCR in 20 ASDs and 20 controls to confirm the microarray gene expression profiling results. The average NRG2 gene expression level in patients with ASD (3.23 ± 2.80) was significantly lower than that in the controls (9.27 ± 4.78, p < 0.001). Next, we conducted resequencing of all the exons of NRG2 in a sample of 349 individuals with ASD, aiming to identify variants of the NRG2 associated with ASD. We identified three variants, including two single nucleotide variants (SNVs), IVS3 + 13A > G (rs889022) and IVS10 + 32T > A (rs182642591), and one small deletion at exon 11 of NRG2 (delGCCCGG, rs933769137). Using data from the Taiwan Biobank as the controls, we found no significant differences in allele frequencies of rs889022 and rs182642591 between two groups. However, there is a significant difference in the genotype and allele frequency distribution of rs933769137 between ASDs and controls (p < 0.0001). The small deletion is located in the EGF-like domain at the C-terminal of the NRG2 precursor protein. Our findings suggest that NRG2 might be a susceptibility gene for ASD.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neurregulinas / Trastorno del Espectro Autista Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neurregulinas / Trastorno del Espectro Autista Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2024 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Suiza