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miR-29s的表观遗传调控影响奶牛乳腺上皮细胞的泌乳活性。

Epigenetic Regulation of miR-29s Affects the Lactation Activity of Dairy Cow Mammary Epithelial Cells.

作者信息

Bian Yanjie, Lei Yu, Wang Chunmei, Wang Jie, Wang Lina, Liu Lili, Liu Lixin, Gao Xuejun, Li Qingzhang

机构信息

Research Department of Lactation Biology and Regulation of Mammary Gland Function, Northeast Agricultural University, Harbin, 150030, China.

Key Laboratory of Dairy Science of Ministry of Education, Northeast Agricultural University, Harbin, 150030, China.

出版信息

J Cell Physiol. 2015 Sep;230(9):2152-63. doi: 10.1002/jcp.24944.

Abstract

Milk is important for human nutrition, and enhanced milk quality has become a major selection criterion for the genetic improvement of livestock. Epigenetic modifications have been shown to be involved in mammary gland development; but the mechanisms underlying their effects remain unknown. MicroRNAs are involved in the regulation of milk synthesis and in mammary gland development. Our study is the first to investigate the roles of miR-29s and epigenetic regulation in dairy cow mammary epithelial cells (DCMECs). Our results show that miR-29s regulate the DNA methylation level by inversely targeting both DNMT3A and DNMT3B in DCMECs. The inhibition of miR-29s caused global DNA hypermethylation and increased the methylation levels of the promoters of important lactation-related genes, including casein alpha s1 (CSN1S1), E74-like factor 5 (ElF5), peroxisome proliferator-activated receptor gamma (PPARγ), sterol regulatory element binding protein-1 (SREBP1), and glucose transporter 1 (GLUT1). The inhibition of miR-29s reduced the secretion of lactoprotein, triglycerides (TG) and lactose by DCMECs. Moreover, the treatment of DCMECs with 5-aza-2'-deoxycytidine (5-Aza-dC) decreased the methylation levels of the miR-29b promoter and increased the expression of miR-29b. The link between miR-29s and DNMT3A/3B enhances our understanding of the roles of miRNAs in mammary gland function, and our data will inform more experimentally oriented studies to identify new mechanisms of regulating lactation. We present new insights regarding the epigenetic regulation of lactation performance. Improved understanding of the molecular basis of lactation will aid in the development of strategies for optimizing milk quality in dairy cows and modifying the lactation performance of offspring.

摘要

牛奶对人类营养至关重要,提高牛奶品质已成为家畜遗传改良的主要选择标准。表观遗传修饰已被证明参与乳腺发育,但其作用机制尚不清楚。微小RNA参与牛奶合成的调控以及乳腺发育。我们的研究首次探讨了miR-29s和表观遗传调控在奶牛乳腺上皮细胞(DCMECs)中的作用。我们的结果表明,miR-29s通过反向靶向DCMECs中的DNMT3A和DNMT3B来调节DNA甲基化水平。抑制miR-29s会导致全基因组DNA高甲基化,并增加重要泌乳相关基因启动子的甲基化水平,这些基因包括酪蛋白αs1(CSN1S1)、E74样因子5(ElF5)、过氧化物酶体增殖物激活受体γ(PPARγ)、固醇调节元件结合蛋白-1(SREBP1)和葡萄糖转运蛋白1(GLUT1)。抑制miR-29s会减少DCMECs中乳蛋白、甘油三酯(TG)和乳糖的分泌。此外,用5-氮杂-2'-脱氧胞苷(5-Aza-dC)处理DCMECs会降低miR-29b启动子的甲基化水平并增加miR-29b的表达。miR-29s与DNMT3A/3B之间的联系加深了我们对微小RNA在乳腺功能中作用的理解,我们的数据将为更多以实验为导向的研究提供信息,以确定调节泌乳的新机制。我们提出了关于泌乳性能表观遗传调控的新见解。对泌乳分子基础的更好理解将有助于制定优化奶牛牛奶品质和改变后代泌乳性能的策略。

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