The RNA-binding protein HuR is a negative regulator in adipogenesis

Autor: Bryan C. Tan, Sook Yoong Chia, Yen Ching Lim, Arcinas Camille Esther Walet, Ufuk Degirmenci, Diana Teh Chee Siang, Lei Sun, Khaing Nwe Win, Xiang Hu, Dan Xu, Aung Maung Maung Kyaw
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
Male
Molecular biology
Adipose Tissue
White

Science
Regulator
General Physics and Astronomy
Repressor
Adipose tissue
White adipose tissue
Biology
General Biochemistry
Genetics and Molecular Biology

Article
ELAV-Like Protein 1
03 medical and health sciences
chemistry.chemical_compound
Gene Knockout Techniques
0302 clinical medicine
Endocrinology
Adipose Tissue
Brown

Adipocyte
Glucose Intolerance
Developmental biology
Animals
Humans
lcsh:Science
Regulation of gene expression
Inflammation
Mice
Knockout

Gene knockdown
Multidisciplinary
Adipogenesis
Intracellular Signaling Peptides and Proteins
Membrane Proteins
RNA-Binding Proteins
Endocrine system and metabolic diseases
General Chemistry
Cell biology
Mice
Inbred C57BL

030104 developmental biology
chemistry
Adipose Tissue
Gene Expression Regulation
030220 oncology & carcinogenesis
lcsh:Q
Insulin Resistance
Zdroj: Nature Communications, Vol 11, Iss 1, Pp 1-13 (2020)
Nature Communications
ISSN: 2041-1723
Popis: Human antigen R (HuR) is an essential regulator of RNA metabolism, but its function in metabolism remains unclear. This study identifies HuR as a major repressor during adipogenesis. Knockdown and overexpression of HuR in primary adipocyte culture enhances and inhibits adipogenesis in vitro, respectively. Fat-specific knockout of HuR significantly enhances adipogenic gene program in adipose tissues, accompanied by a systemic glucose intolerance and insulin resistance. HuR knockout also results in depot-specific phenotypes: it can repress myogenesis program in brown fat, enhance inflammation program in epidydimal white fat and induce browning program in inguinal white fat. Mechanistically, HuR may inhibit adipogenesis by recognizing and modulating the stability of hundreds of adipocyte transcripts including Insig1, a negative regulator during adipogenesis. Taken together, our work establishes HuR as an important posttranscriptional regulator of adipogenesis and provides insights into how RNA processing contributes to adipocyte development.
Human antigen R (HuR) is an RNA binding protein that promotes mRNA stability. Here the authors show that HuR represses adipogenesis in white and brown adipose tissue by stabilizing Insig1 and other targets.
Databáze: OpenAIRE