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MBD4基因在猪脂肪细胞分化中起重要作用。

The MBD4 gene plays an important role in porcine adipocyte differentiation.

作者信息

Zhang Lian-Jiang, Zhu Ya-Nan, Gao Yan, Liu Si-Yuan, Zhai Bo, Li Chang-Hong, Liu Hui-Yu, Chen Jian, Yuan Bao, Dai Li-Sheng, Zhang Jia-Bao

机构信息

College of Animal Sciences, Jilin University, Changchun, China.

出版信息

Cell Physiol Biochem. 2014;34(4):1216-26. doi: 10.1159/000366333. Epub 2014 Sep 25.

Abstract

BACKGROUND

MBD4 (methyl-CpG binding domain protein 4) is an important G: T glycosylase that can identify T-G mismatches. It plays a role in active demethylation through base excision repair. Overexpression of MBD4 gene can cause the demethylation of numerous genes, and the remethylation of MBD4-associated genes can occur when the MBD4 gene is knocked out. To date, the functions and regulatory mechanisms of the MBD4 gene in the differentiation of porcine preadipocytes have not been clearly established.

METHODS

Subcutaneous fat cells from 1- to 7-day-old Junmu-1 piglets were cultured in vitro, induced to differentiate, and then identified. A real-time fluorescence-based quantitative polymerase chain reaction (PCR) analysis was conducted to detect MBD4 messenger RNA (mRNA) expression. Cells were treated with MBD4-siRNA (small interfering RNA) and induced to differentiate. Changes in the lipid droplets were observed by oil red O staining. Changes in the mRNA and protein expression levels of MBD4 and the adipose differentiation-associated genes C/EBPα (CCAAT-enhancer-binding protein alpha), PPARγ (peroxisome proliferator-activated receptor gamma), and aP2 (adipocyte protein 2) were detected. In addition, the bisulfite sequencing method was used to detect changes in methylation in the promoters of certain genes associated with adipose differentiation.

RESULTS

Levels of MBD4 mRNA and protein expression varied with time over the course of the porcine adipocyte differentiation, with the highest levels of this expression observed on day two of the differentiation process. After silencing MBD4 and inducing differentiation, the production of lipid droplets decreased, the mRNA expression levels of C/EBPα, PPARγ, and aP2 were significantly reduced, and DNA methylation modification levels were significantly elevated in the examined promoter regions.

CONCLUSION

The silencing of the MBD4 gene can influence the DNA methylation levels of preadipocyte differentiation-related genes and subsequently inhibit the differentiation of porcine preadipocytes.

摘要

背景

MBD4(甲基-CpG结合域蛋白4)是一种重要的G:T糖基化酶,可识别T-G错配。它通过碱基切除修复在主动去甲基化过程中发挥作用。MBD4基因的过表达可导致众多基因去甲基化,而当MBD4基因被敲除时,与MBD4相关的基因会发生重新甲基化。迄今为止,MBD4基因在猪前体脂肪细胞分化中的功能和调控机制尚未明确。

方法

取1至7日龄军牧1号仔猪的皮下脂肪细胞进行体外培养、诱导分化并鉴定。采用实时荧光定量聚合酶链反应(PCR)分析检测MBD4信使核糖核酸(mRNA)表达。用MBD4小干扰RNA(siRNA)处理细胞并诱导分化。通过油红O染色观察脂滴变化。检测MBD4以及脂肪分化相关基因C/EBPα(CCAAT增强子结合蛋白α)、PPARγ(过氧化物酶体增殖物激活受体γ)和aP2(脂肪细胞蛋白2)的mRNA和蛋白表达水平变化。此外,采用亚硫酸氢盐测序法检测与脂肪分化相关的某些基因启动子区域的甲基化变化。

结果

在猪脂肪细胞分化过程中,MBD4 mRNA和蛋白表达水平随时间变化,在分化过程的第2天观察到该表达水平最高。沉默MBD4并诱导分化后,脂滴生成减少,C/EBPα、PPARγ和aP2的mRNA表达水平显著降低,在所检测的启动子区域DNA甲基化修饰水平显著升高。

结论

MBD4基因沉默可影响前体脂肪细胞分化相关基因的DNA甲基化水平,进而抑制猪前体脂肪细胞的分化。

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