| Literature DB >> 33763417 |
Kaihui Zhang1,2,3, Wenxing Sun4, Yi Liu2, Yuqiang Lv2, Daisen Hou1,3, Yan Lin1,3,5, Wei Xu1,3,5, Jianyuan Zhao1,3,5, Zhongtao Gai2, Shimin Zhao1,3,5, Yiyuan Yuan1,3.
Abstract
Nonsense variants in KIDINS220/ARMS were identified as the main cause of spastic paraplegia, intellectual disability, nystagmus, and obesity (SINO) syndrome, a rare disease with birth defects in brachycephaly, neurological disorder, and obesity. The cause of neural cell dysfunction by KIDINS220/ARMS were extensively studied while the cause of obesity in SINO syndrome remains elusive. Here, we identified KIDINS220/ARMS as an adipocyte differentiation-regulating gene. A Chinese family, mother and her two sons, all showed severe symptoms of SINO syndrome. G-banding karyotyping, chromosome microarray analysis, and whole exome sequencing revealed a novel amber mutation, c.3934G>T (p. E1312X), which was close to the C-terminal region of KIDINS220/ARMS and resulted in the premature of the protein. Both the mRNA and protein levels of KIDINS220/ARMS gradually decreased during adipocyte differentiation. Knockdown of KINDINS220/ARMS could prompt adipocyte differentiation and lipid accumulation while overexpression of KIDINS220/ARMS decrease the rate of matured adipocytes. Furthermore, we demonstrated that KIDINS220/ARMS inhibits adipocyte maturation through sustained extracellular signal-regulated kinase signaling. In conclusion, this is the first report about a vertical heredity of severe dominant pathogenic mutation of KIDINS220/ARMS, suggested that KIDINS220/ARMS played a negative role in adipocyte maturation, explained the cause of obesity in SINO syndrome and could highlight the importance of adipocyte differentiation in neuron functions.Entities:
Keywords: KIDINS220/ARMS; SINO syndrome; adipocyte differentiation; brachycephaly; intellectual disability; obesity
Year: 2021 PMID: 33763417 PMCID: PMC7982959 DOI: 10.3389/fcell.2021.619475
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X