The association of CNTNAP2 rs2710102 and ENGRAILED-2 rs1861972 genes polymorphism and autism in Iranian population

被引:7
作者
Beiranvandi, Fatemeh [1 ]
Akouchekian, Mansoureh [2 ]
Javadi, Gholam Reza [1 ]
Darvish, Hossein [3 ]
机构
[1] Islamic Azad Univ, Dept Biol, Sci & Res Branch, Tehran, Iran
[2] Iran Univ Med Sci, Sch Med, Dept Med Genet & Mol Biol, Tehran, Iran
[3] Semnan Univ Med Sci, Canc Res Ctr, Semnan, Iran
关键词
HOMEOBOX TRANSCRIPTION FACTOR; SPECTRUM; EPIDEMIOLOGY; LANGUAGE;
D O I
10.1016/j.mgene.2020.100664
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Autism spectrum disorder (ASD) is a highly heritable neurodevelopment disease characterized by impaired social interactions, communication deficits, restricted interests, stereotyped and repetitive behaviors, which results from the interaction between genetic vulnerability and environmental factors. Our study was aimed to explore the association between CNTNAP2 gene polymorphism (rs2710102 C/T) and ENGRAILED-2 (EN2) (rs1861972 A/G) with the risk of autism in the Iranian population. A total of 67 autism cases and 100 controls were recruited. Single nucleotide polymorphism (SNP) rs2710102 C/T was genotyped by utilizing polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and SNP rs1861972 A/G was genotyped by using Tetra-primer ARMS-PCR. The results of this study showed that there is no significant association between rs2710102 CNTNAP2 gene polymorphism and autism, but there is a significant association between rs1861972 EN2 gene polymorphism and autism in the studied population. Consequently, our data provide evidence that the EN2 gene may be implicated in the predisposition to autism in the Iranian population.
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页数:4
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