Jain R G, Andrews L G, McGowan K M, Pekala P H, Keene J D
Department of Biochemistry, School of Medicine, East Carolina University, Greenville, North Carolina 27834, USA.
Mol Cell Biol. 1997 Feb;17(2):954-62. doi: 10.1128/MCB.17.2.954.
3T3-L1 preadipocytes ectopically expressing the mammalian RNA-binding protein Hel-N1 expressed up to 10-fold more glucose transporter (GLUT1) protein and exhibited elevated rates of basal glucose uptake. Hel-N1 is a member of the ELAV-like family of proteins associated with the induction and maintenance of differentiation in various species. ELAV proteins are known to bind in vitro to short stretches of uridylates in the 3' untranslated regions (3'UTRs) of unstable mRNAs encoding growth-regulatory proteins involved in transcription and signal transduction. GLUT1 mRNA also contains a large 3'UTR with a U-rich region that binds specifically to Hel-N1 in vitro. Analysis of the altered GLUT1 expression at the translational and posttranscriptional levels suggested a mechanism involving both mRNA stabilization and accelerated formation of translation initiation complexes. These findings are consistent with the hypothesis that the Hel-N1 family of proteins modulate gene expression at the level of mRNA in the cytoplasm.
异位表达哺乳动物RNA结合蛋白Hel-N1的3T3-L1前脂肪细胞表达的葡萄糖转运蛋白(GLUT1)蛋白多出近10倍,并表现出基础葡萄糖摄取率升高。Hel-N1是ELAV样蛋白家族的成员,与多种物种的分化诱导和维持相关。已知ELAV蛋白在体外可与编码参与转录和信号转导的生长调节蛋白的不稳定mRNA的3'非翻译区(3'UTR)中的短尿苷酸片段结合。GLUT1 mRNA也含有一个大的3'UTR,其富含尿苷酸的区域在体外可与Hel-N1特异性结合。对翻译和转录后水平上GLUT1表达变化的分析提示了一种涉及mRNA稳定和翻译起始复合物加速形成的机制。这些发现与Hel-N1蛋白家族在细胞质中mRNA水平调节基因表达的假说一致。