Department of Neuroscience and Rehabilitation, Section of Medical Biochemistry, Molecular Biology and Genetics, University of Ferrara, Ferrara, Italy.
School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
Birth Defects Res. 2021 Dec 1;113(20):1463-1469. doi: 10.1002/bdr2.1959. Epub 2021 Oct 19.
The medial and maxillary aspects of the upper lip originate at separate embryonic stages and therefore may experience different maternal exposure patterns which may affect methylation. Based on this hypothesis, we investigated the level of methylation of the methylene tetrahydrofolate reductase promoter gene (mMTHFR) in tissues from cleft lip, and mMTHFR levels by MTHFR c.677C > T genotype. We further investigated whether mMTHFR mitigates the effect of smoking on long interspersed nuclear element (LINE-1) methylation in these tissues.
DNA extracted from medial and lateral tissues of 26 infants with nonsyndromic cleft lip with or without cleft palate (nsCL/P) was bisulfite converted and mMTHFR was measured on a pyrosequenser. LINE-1 methylation and MTHFR c.677C > T genotype data were obtained in our previous study.
There was no substantial difference in mMTHFR (p = .733) and LINE-1 (p = .148) between the two tissues. mMTHFR was not influenced by MTHFR c.677C > T genotype, but there was suggestive evidence that the difference was larger among infants exposed to maternal smoking compared to nonexposed. LINE-1 methylation differences were significant (p = .025) in infants born to nonsmoking mothers, but this was not apparent (p = .872) in infants born to mothers who smoked. Our Pearson's correlation analysis suggested a weak inverse association between mMTHFR and LINE-1 (r = -.179, p = .381).
Our preliminary observation of differences in patterns of mMTHFR levels in lip tissue suggests the interplay of gene and environment in the establishment of methylation in tissues at both sides of cleft lip. This requires investigation in a larger cohort, integrated with metabolic assessment.
上唇的内侧和上颌侧方在胚胎发育的不同阶段起源,因此可能经历不同的母体暴露模式,这可能会影响甲基化。基于这一假设,我们研究了唇裂组织中亚甲基四氢叶酸还原酶启动子基因(mMTHFR)的甲基化水平以及 mMTHFR c.677C>T 基因型。我们进一步研究了 mMTHFR 是否减轻了这些组织中吸烟对长散布核元件(LINE-1)甲基化的影响。
从 26 名非综合征性唇裂伴或不伴腭裂(nsCL/P)婴儿的内侧和外侧组织中提取 DNA,用亚硫酸氢盐进行转化,并在 pyrosequenser 上测量 mMTHFR。LINE-1 甲基化和 MTHFR c.677C>T 基因型数据是在我们之前的研究中获得的。
两个组织之间的 mMTHFR(p=0.733)和 LINE-1(p=0.148)没有显著差异。MTHFR 不受 MTHFR c.677C>T 基因型的影响,但有迹象表明,在暴露于母体吸烟的婴儿中,这种差异比未暴露于母体吸烟的婴儿更大。在不吸烟母亲所生的婴儿中,LINE-1 甲基化差异具有显著性(p=0.025),但在吸烟母亲所生的婴儿中,这种差异并不明显(p=0.872)。我们的 Pearson 相关分析表明,mMTHFR 与 LINE-1 之间存在微弱的负相关(r=-0.179,p=0.381)。
我们对上唇组织中 mMTHFR 水平模式差异的初步观察表明,基因和环境在唇裂两侧组织的甲基化建立过程中相互作用。这需要在更大的队列中进行研究,并与代谢评估相结合。