Lin Nien-Yi, Lin Chung-Tien, Chen Yu-Ling, Chang Ching-Jin
Department and Graduate Institute of Veterinary Medicine, College of Bio-Resources and Agriculture, National Taiwan University, Taipei, Taiwan.
FEBS J. 2007 Feb;274(3):867-78. doi: 10.1111/j.1742-4658.2007.05632.x.
Tristetraprolin is a zinc-finger-containing RNA-binding protein. Tristetraprolin binds to AU-rich elements of target mRNAs such as proto-oncogenes, cytokines and growth factors, and then induces mRNA rapid degradation. It was observed as an immediate-early gene that was induced in response to several kinds of stimulus, such as insulin and other growth factors and stimulators of innate immunity such as lipopolysaccharides. We observed that tristetraprolin was briefly expressed during a 1-8 h period after induction of differentiation in 3T3-L1 preadipocytes. Detailed analysis showed that tristetraprolin mRNA expression was stimulated by fetal bovine serum and differentiation inducers, and was followed by rapid degradation. The 3'UTR of tristetraprolin mRNAs contain adenine- and uridine-rich elements. Biochemical analyses using RNA pull-down, RNA immunoprecipitation and gel shift experiments demonstrated that adenine- and uridine-rich element-binding proteins, HuR and tristetraprolin itself, were associated with tristetraprolin adenine- and uridine-rich elements. Functional characterization confirmed that tristetraprolin negatively regulated its own expression. Thus, our results indicated that the tight autoregulation of tristetraprolin expression correlated with its critical functional role in 3T3-L1 differentiation.
锌指蛋白Tristetraprolin是一种含RNA结合蛋白。Tristetraprolin与原癌基因、细胞因子和生长因子等靶mRNA的富含AU元件结合,进而诱导mRNA快速降解。它被视为一种即刻早期基因,可响应多种刺激而被诱导,如胰岛素和其他生长因子,以及脂多糖等先天免疫刺激剂。我们观察到,在3T3-L1前脂肪细胞诱导分化后的1-8小时内,Tristetraprolin短暂表达。详细分析表明,Tristetraprolin mRNA表达受胎牛血清和分化诱导剂刺激,随后快速降解。Tristetraprolin mRNA的3'UTR含有富含腺嘌呤和尿嘧啶的元件。使用RNA下拉、RNA免疫沉淀和凝胶迁移实验进行的生化分析表明,富含腺嘌呤和尿嘧啶元件结合蛋白HuR和Tristetraprolin本身与Tristetraprolin富含腺嘌呤和尿嘧啶的元件相关。功能表征证实,Tristetraprolin对其自身表达起负调控作用。因此,我们的结果表明,Tristetraprolin表达的严格自我调节与其在3T3-L1分化中的关键功能作用相关。