Abstract:Objective To investigate the features of methylation in the promoter region of glucose-6-phosphate dehydrogenase (G6PD) gene and the association between gene promoter methylation and G6PD deficiency. Methods Fluorescent quantitative PCR was used to measure the mRNA expression of G6PD in 130 children with G6PD deficiency. Sixty-five children without G6PD deficiency served as the control group. The methylation-sensitive high-resolution melting curve analysis and bisulfite PCR sequencing were used to analyze gene promoter methylation in 22 children with G6PD deficiency and low G6PD mRNA expression. The G6PD gene promoter methylation was analyzed in 44 girls with normal G6PD mRNA expression (7 from G6PD deficiency group and 37 from control group). Results Twenty-two (16.9%) children with G6PD deficiency had relatively low mRNA expression of G6PD; among whom, 16 boys showed no methylation, and 6 girls showed partial methylation. Among the 44 girls with normal G6PD mRNA expression, 40 showed partial methylation, and 4 showed no methylation (1 case in the G6PD group and 3 cases in the control group). Conclusions Gene promoter methylation is not associated with G6PD deficiency in boys. Girls have partial methylation or no methylation in the G6PD gene, suggesting that the methylation may be related to G6PD deficiency in girls.
Minucci A, Moradkhani K, Hwang MJ, et al. Glucose-6-phosphate dehydrogenase(G6PD) mutations database: review of the "old" and update of the new mutations[J]. Blood Cells Mol Dis, 2012, 48(3): 154-165.
Jiang W, Yu G, Liu P, et al. Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese population[J]. Hum Genet, 2006, 119(5): 463-478.
[5]
Yan JB, Xu HP, Xiong C, et al. Rapid and reliable detection of glucose-6-phosphate dehydrogenase (G6PD) gene mutations in Han Chinese using high-resolution melting analysis[J]. J Mol Diagn, 2010, 12(3): 305-311.
[6]
Portela A, Esteller M. Epigenetic modifications and human disease[J]. Nat Biotechnol, 2010, 20(8): 1057-1068.
Gendrel AV, Heard E. Fifty years of X-inactivation research[J]. Development, 2011, 138(23): 5049-5055.
[9]
Carrel L, Willard HF. X-inactivation profile reveals extensive variability in X-linked gene expression in females[J]. Nature, 2005, 434(7031): 400-404.
[10]
Cotton AM, Lam L, Affleck JG, et al. Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation[J]. Hum Genet, 2011, 130(2): 187-201.
[11]
Cotton AM, Avila L, Penaherrera MS, et al. Inactive X chromosome-specific reduction in placental DNA methylation[J]. Hum Mol Genet, 2009, 18(19): 3544-3552.
[12]
Zhang Y, Castillo-Morales A, Jiang M, et al. Genes that escape X-inactivation in humans have high intraspecific variability in expression, are associated with mental impairment but are not slow evolving[J]. Mol Biol Evol, 2013, 30(12): 2588-2601.
[13]
Wojdacz TK, Dobrovic A. Methylation-sensitive high resolution melting (MS-HRM): a new approach for sensitive and highthroughput assessment of methylation[J]. Nucleic Acids Res, 2007, 35(6): e41.
[14]
Mastoraki S, Chimonidou M, Dimitrakopoulos L, et al. A rapid and accurate closed-tube Methylation-Sensitive High Resolution MeltingAnalysis assay for the semi-quantitative determination of SOX17 promoter methylation in clinical samples[J]. Clin Chim Acta, 2015, 444: 303-309.
[15]
Candiloro IL, Mikeska T, Dobrovic A. Assessing combined methylat ion-sensit ive high resolu t ion me l ting and pyrosequencing for the analysis of heterogeneous DNA methylation[J]. Epigenetics, 2011, 6(4): 500-507.