| Literature DB >> 30389664 |
Juncheng Wei1, Lu Chen2, Fei Li1, Yanzhi Yuan3, Yajun Wang1, Wanjun Xia4, Yuehui Zhang3, Yuanming Xu1, Zhao Yang5, Beixue Gao1, Chaozhi Jin3, Johanna Melo-Cardenas1, Richard M Green6, Hui Pan7, Jian Wang8, Fuchu He8, Kezhong Zhang9, Deyu Fang10,11.
Abstract
The endoplasmic reticulum-associated protein degradation (ERAD) is responsible for recognizing and retro-translocating protein substrates, misfolded or not, from the ER for cytosolic proteasomal degradation. HMG-CoA Reductase (HMGCR) Degradation protein-HRD1-was initially identified as an E3 ligase critical for ERAD. However, its physiological functions remain largely undefined. Herein, we discovered that hepatic HRD1 expression is induced in the postprandial condition upon mouse refeeding. Mice with liver-specific HRD1 deletion failed to repress FGF21 production in serum and liver even in the refeeding condition and phenocopy the FGF21 gain-of-function mice showing growth retardation, female infertility, and diurnal circadian behavior disruption. HRD1-ERAD facilitates the degradation of the liver-specific ER-tethered transcription factor CREBH to downregulate FGF21 expression. HRD1-ERAD catalyzes polyubiquitin conjugation onto CREBH at lysine 294 for its proteasomal degradation, bridging a multi-organ crosstalk in regulating growth, circadian behavior, and female fertility through regulating the CREBH-FGF21 regulatory axis.Entities:
Keywords: CREBH; ER‐associated degradation; FGF21; HRD1; multi‐organ crosstalk
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Year: 2018 PMID: 30389664 PMCID: PMC6236336 DOI: 10.15252/embj.201898942
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598