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EEF1D 通过调节哺乳动物中的 PI3K-Akt 信号促进乳脂合成。

EEF1D facilitates milk lipid synthesis by regulation of PI3K-Akt signaling in mammals.

机构信息

China National Center for Bioinformation, Beijing, China.

CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.

出版信息

FASEB J. 2021 May;35(5):e21455. doi: 10.1096/fj.202000682RR.

Abstract

Mammal's milk is an abundantly foremost source of proteins, lipids, and micronutrients for human nutrition and health. Understanding the molecular mechanisms underlying synthesis of milk components provides practical benefits to improve the milk quality via systematic breeding program in mammals. Through RNAi with EEF1D in primary bovine mammary epithelial cells, we phenotypically observed aberrant formation of cytoplasmic lipid droplets and significantly decreased milk triglyceride level by 37.7%, and exploited the mechanisms by which EEF1D regulated milk lipid synthesis via insulin (PI3K-Akt), AMPK, and PPAR pathways. In the EEF1D CRISPR/Cas9 knockout mice, incompletely developed mammary glands at 9th day postpartum with small or unformed lumens, and significantly decreased triglyceride concentration in milk by 23.4% were observed, as well as the same gene expression alterations in the three pathways. For dairy cattle, we identified a critical regulatory mutation modifying EEF1D transcription activity, which interpreted 7% of the genetic variances of milk lipid yield and percentage. Our findings highlight the significance of EEF1D in mammary gland development and milk lipid synthesis in mammals.

摘要

哺乳动物的奶是人类营养和健康的蛋白质、脂质和微量营养素的丰富首要来源。了解乳成分合成的分子机制为通过哺乳动物的系统选育计划来提高奶质量提供了实际的益处。通过在原代牛乳腺上皮细胞中用 EEF1D 的 RNAi,我们表型上观察到细胞质脂滴的异常形成,并且乳甘油三酯水平显著降低了 37.7%,并通过胰岛素 (PI3K-Akt)、AMPK 和 PPAR 途径研究了 EEF1D 调节乳脂质合成的机制。在 EEF1D CRISPR/Cas9 敲除小鼠中,产后第 9 天观察到乳腺发育不完全,腔小或不成形,并且乳中甘油三酯浓度显著降低了 23.4%,三个途径中的基因表达也发生了同样的改变。对于奶牛,我们鉴定出了一个关键的调节突变,修饰了 EEF1D 的转录活性,该突变解释了 7%的乳脂产量和百分比的遗传变异。我们的研究结果强调了 EEF1D 在哺乳动物乳腺发育和乳脂质合成中的重要性。

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