Dibrov Alexander, Kashour Tarek, Amara Francis M
University of Manitoba, Winnipeg, Man., Canada.
Growth Factors. 2006 Mar;24(1):1-11. doi: 10.1080/08977190500365995.
Transforming growth factor beta (TGF-beta) is a biologically multipotent regulatory protein implicated in functions that include the regulation of cellular growth, differentiation, extracellular matrix formation, and wound healing. It also plays a role in the pathologies of Alzheimer's disease, cancer and autoimmune disorders. TGF-beta modulates gene expression by affecting transcriptional activation and mRNA turnover rate. Steady-state mRNA levels depend on both the transcriptional activity and mRNA half-life. The stability of mRNA can be modified by the binding of trans-acting factors to cis-elements on the message. These can protect the mRNA from cleavage by RNAses, or they may promote mRNA cleavage. Changes in mRNA stability can lead to changes in the proteome and subsequently in cellular metabolism. The SMAD family of proteins has been implicated in the transduction of the TGF-beta signal, where they regulate transcriptional activity. This review attempts to provide new insights into the role played by TGF-beta in the regulation of mRNA turnover.
转化生长因子β(TGF-β)是一种具有多种生物学功能的调节蛋白,参与细胞生长、分化、细胞外基质形成和伤口愈合等过程的调节。它在阿尔茨海默病、癌症和自身免疫性疾病的病理过程中也发挥作用。TGF-β通过影响转录激活和mRNA周转速率来调节基因表达。稳态mRNA水平取决于转录活性和mRNA半衰期。mRNA的稳定性可通过反式作用因子与信息上的顺式元件结合而改变。这些作用可以保护mRNA不被核糖核酸酶切割,也可能促进mRNA切割。mRNA稳定性的变化可导致蛋白质组的变化,进而影响细胞代谢。SMAD蛋白家族参与TGF-β信号的转导,在其中调节转录活性。本综述旨在为TGF-β在mRNA周转调节中的作用提供新的见解。