Study on the methylation of ENO2 gene in peripheral blood in children with autism spectrum disorder

JIANG Lian, MA Chen-huan, FANG Yu-dan, WEI Nian-jin, CHEN Feng-feng, PAN Li-zhu, WANG Yu

Chinese Journal of Child Health Care ›› 2020, Vol. 28 ›› Issue (9) : 985-988.

PDF(1327 KB)
PDF(1327 KB)
Chinese Journal of Child Health Care ›› 2020, Vol. 28 ›› Issue (9) : 985-988. DOI: 10.11852/zgetbjzz2019-1920

Study on the methylation of ENO2 gene in peripheral blood in children with autism spectrum disorder

  • JIANG Lian, MA Chen-huan, FANG Yu-dan, WEI Nian-jin, CHEN Feng-feng, PAN Li-zhu, WANG Yu
Author information +
History +

Abstract

Objective To explore the methylation modification of ENO2 gene in peripheral blood of children with autism spectrum disorder (ASD),in order to provide theoretical evidence for early screening of ASD. Method Peripheral blood from ASD children and control children were collected to analyze differential methylation by methylated-DNA immunoprecipitation (MeDIP) chips. One neuron-specific gene,ENO2,was found to be hypermethylated in the autistic samples. In addition,obtained blood samples were collected from 101 autistic children and controls matched with age and sex. This difference was validated by bisulfite sequencing PCR (BSP). The differential expression of ENO2 gene was further analyzed by real-time quantitative polymerase chain reaction (RT-qPCR) and ELISA. Results The hypermethylation of ENO2 within the promoter region was confirmed by BSP to be present in 15.8% (16/101) of the autistic samples. The methylation frequency of 16 CpG sites of ENO2 gene promoter was calculated,and it was found that the closer the promoter was to the start site of transcription,the higher the methylation frequency would be. The mean level of ENO2 RNA in these 16 autistic samples was reduced by 30% approximately compared with that in controls. The average level of ENO2 protein expression in 16 autistic samples was (15.15±3.52) μg/L,about half of that in the controls[ (33.78±8.18) μg/L]. Conclusions Hypermethylation of ENO2 gene is found in peripheral blood of 15.8% of ASD children. Moreover,reduced level of ENO2 expression may be a biomarker for a subset of autistic children.

Key words

autism spectrum disorder / ENO2 gene / neurodevelopment / methylation / epegenetics

Cite this article

Download Citations
JIANG Lian, MA Chen-huan, FANG Yu-dan, WEI Nian-jin, CHEN Feng-feng, PAN Li-zhu, WANG Yu. Study on the methylation of ENO2 gene in peripheral blood in children with autism spectrum disorder[J]. Chinese Journal of Child Health Care. 2020, 28(9): 985-988 https://doi.org/10.11852/zgetbjzz2019-1920

References

[1] Wang Y,Zhong N.Clinical and genetic heterogeneity of autism.Cooper and Chen (ed) mutations in human genetic disease[M].InTech,Croatia,2012:217-232.
[2] Sven B,Sonya G,Peter B,et al.The contribution of environmental exposure to the etiology of autism spectrum disorder[J].Cell Mol Life Sci,2019,76(7):1275-1297.
[3] Wang Y,Zhao X,Ju W,et al.Genome-wide differential expression of synaptic long non-coding RNAs in autism spectrum disorder[J].Transl Psychiatry,2015,5(10):e660.
[4] Wang Y,Fang YD,Zhang FL,et al.Hypermethylation of the enolase gene (ENO2) in autism[J].Eur J Pediatr,2014,173(9):1233-1244.
[5] Annie VC,Janine L.The landscape of DNA methylation amid a perfect storm of autism aetiologies[J].Nat Rev Neurosci,2016,17(7):411-423
[6] Tremblay MW,Jiang YH.DNA methylation and susceptibility to autism spectrum disorder[J].Annu Rev Med,2019,70:151-166
[7] Junaid MA,Kowal D,Barua M,et al.Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor[J].Am J Med Genet A,2004,131(1):11-17.
[8] Geschwind DH.Advances in autism[J].Annu Rev Med,2009,60:367-380.
[9] Johnson NL,Giarelli E,Lewis C,et al.Genomics and autism spectrum disorder[J].J Nurs Scholarsh,2013,45(1):69-78.
[10] Mill J,Tang T,Kaminsky Z,et al.Epigenomic profiling reveals DNA-methylation changes associated with major psychosis[J].Am J Hum Genet,2008,82(3):696-711.
[11] Eliza W,Mirjam L,Annemieke MW,et al.DNA methylation markers associated with type 2 diabetes,fasting glucose and HbA1c levels:a systematic review and replication in a case-control sample of the Lifelines study[J].Diabetologia,2018,61(2):354-368.
[12] Momeni N,Bergquist J,Brudin L,et al.A novel blood-based biomarker for detection of autism spectrum disorders[J].Transl Psychiatry,2012,2(3):e91.
[13] Schwarz E,Guest PC,Rahmoune H,et al.Sex-specific serum biomarker patterns in adults with Asperger′s syndrome[J].Mol Psychiatry,2011,16(1):1213-1220.
[14] Junaid MA,Kowal D,Barua M,et al.Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor[J].Am J Med Genet A,2004,131(1):11-17.
[15] Shannon R,Dmitriy M,Niyazov,DA,et al.Clinical and molecular characteris-tics of mitochondrial dysfunction in autism spectrum disorder[J].Mol Diagn Ther,2018,22(5):571-593.
PDF(1327 KB)

Accesses

Citation

Detail

Sections
Recommended

/