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Histone acetylation is involved in TCDD-induced cleft palate formation in fetal mice

机译:组蛋白乙酰化参与胎鼠TCDD诱导的left裂形成

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The aim of the present was to evaluate the effects of DNA methylation and histone acetylation on 2,3,7,8-tetrachlo-rodibenzo-p-dioxin (TCDD)-induced cleft palate in fetal mice. Pregnant mice (n= 10) were randomly divided into two groups: i) TCDD group, mice were treated with 28 mu g/kg TCDD on gestation day (GD) 10 by oral gavage; ii) control group, mice were treated with an equal volume of corn oil. On GD 16.5, the fetal mice were evaluated for the presence of a cleft palate. An additional 36 pregnant mice were divided into the control and TCDD groups, and palate samples were collected on GD 13.5, GD 14.5 and GD 15.5, respectively. Transforming growth factor-beta 3 (TGF-beta 3) mRNA expression, TGF-beta 3 promoter methylation, histone acetyltransferase (HAT) activity and histone H3 (H3) acetylation in the palates were evaluated in the two groups. The incidence of a cleft palate in the TCDD group was 93.55%, and no cases of cleft palate were identified in the control group. On GD 13.5 and GD 14.5, TGF-beta 3 mRNA expression, HAT activity and acetylated H3 levels were significantly increased in the TCDD group compared with the control. Methylated bands were not observed in the TCDD or control groups. In conclusion, at the critical period of palate fusion (GD 13.5-14.5), TCDD significantly increased TGF-beta 3 gene expression, HAT activity and H3 acetylation. Therefore, histone acetylation may be involved in TCDD-induced cleft palate formation in fetal mice.
机译:本发明的目的是评估DNA甲基化和组蛋白乙酰化对2,3,7,8-四氯-罗二苯并-p-二恶英(TCDD)诱导的胎鼠c裂的影响。将怀孕的小鼠(n = 10)随机分为两组:i)TCDD组,在妊娠第10天,通过口服管饲法以28μg/ kg TCDD治疗小鼠; ii)对照组,用等体积的玉米油治疗小鼠。在GD 16.5上,评估胎鼠是否存在left裂。将另外36只怀孕的小鼠分为对照组和TCDD组,分别在GD 13.5,GD 14.5和GD 15.5上收集pa样品。在两组中评估了上颚中转化生长因子-β3(TGF-β3)mRNA表达,TGF-β3启动子甲基化,组蛋白乙酰转移酶(HAT)活性和组蛋白H3(H3)乙酰化。 TCDD组的pa裂发生率为93.55%,对照组中未发现cases裂病例。与对照组相比,TCDD组在GD 13.5和GD 14.5上TGF-β3mRNA表达,HAT活性和乙酰化H3水平显着增加。在TCDD组或对照组中未观察到甲基化带。总之,在上颚融合的关键时期(GD 13.5-14.5),TCDD显着增加了TGF-β3基因的表达,HAT活性和H3乙酰化。因此,组蛋白乙酰化可能参与了TCDD诱导的胎鼠c裂的形成。

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