Recommended Citation
Jia, Zhihao; Yue, Feng; Chen, Xiyue; Narayanan, Naagarajan; Qiu, Jiamin; Syed, Sabriya A.; Imbalzano, Anthony N.; Deng, Meng; Yu, Peng; Hu, Changdeng; and Kuang, Shihuan, "Protein Arginine Methyltransferase PRMT5 Regulates Fatty Acid Metabolism and Lipid Droplet Biogenesis in White Adipose Tissues" (2020). Purdue University Libraries Open Access Publishing Fund. Paper 139.
http://dx.doi.org/10.1002/advs.202002602
DOI
10.1002/advs.202002602
Date of this Version
10-16-2020
Abstract
The protein arginine methyltransferase 5 (PRMT5) is an emerging regulator of cancer and stem cells including adipogenic progenitors. Here, a new physiological role of PRMT5 in adipocytes and systemic metabolism is reported. Conditional knockout mice were generated to ablate the Prmt5 gene specifically in adipocytes (Prmt5AKO). The Prmt5AKO mice exhibit sex- and depot-dependent progressive lipodystrophy that is more pronounced in females and in visceral (than subcutaneous) white fat. The lipodystrophy and associated energy imbalance, hyperlipidemia, hepatic steatosis, glucose intolerance, and insulin resistance are exacerbated by high-fat-diet. Mechanistically, Prmt5 methylates and releases the transcription elongation factor SPT5 from Berardinelli-Seip congenital lipodystrophy 2 (Bscl2, encoding Seipin) promoter, and Prmt5AKO disrupts Seipin-mediated lipid droplet biogenesis. Prmt5 also methylates Sterol Regulatory Element-Binding Transcription Factor 1a (SREBP1a) and promotes lipogenic gene expression, and Prmt5AKO suppresses SREBP1a-dependent fatty acid metabolic pathways in adipocytes. Thus, PRMT5 plays a critical role in regulating lipid metabolism and lipid droplet biogenesis in adipocytes.
Comments
This is the publisher PDF of Jia, Z.; Yue, F.; Chen, X.; et al (2020) Protein Arginine Methyltransferase PRMT5 Regulates Fatty Acid Metabolism and Lipid Droplet Biogenesis in White Adipose Tissues Advanced Science 7(23). This article is distributed under a CC-BY license, and is available at DOI: 10.1002/advs.202002602.