Fukada Toshiyuki, Tonks Nicholas K
Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.
EMBO J. 2003 Feb 3;22(3):479-93. doi: 10.1093/emboj/cdg067.
Changes in expression of PTP1B, the prototypic protein tyrosine phosphatase, have been associated with various human diseases; however, the mechanisms by which PTP1B expression is regulated have not been defined. We have identified an enhancer sequence within the PTP1B promoter which serves as a binding site for the transcription factor Y box-binding protein-1 (YB-1). Overexpression of YB-1 resulted in increased levels of PTP1B. Furthermore, depletion of YB-1 protein, by expression of a specific antisense construct, led to an approximately 70% decrease in expression of PTP1B, but no change in the level of its closest relative, TC-PTP. Expression of antisense YB-1 resulted in increased sensitivity to insulin and enhanced signaling through the cytokine receptor gp130, which was suppressed by re-expression of PTP1B. Finally, we observed a correlation between the expression of PTP1B and that of YB-1 in cancer cell lines and an animal model of type II diabetes. Our data reveal an important role for YB-1 as a regulator of PTP1B expression, and further highlight PTP1B as a critical regulator of insulin- and cytokine-mediated signal transduction.
蛋白酪氨酸磷酸酶1B(PTP1B)作为典型的蛋白酪氨酸磷酸酶,其表达变化与多种人类疾病相关;然而,PTP1B表达的调控机制尚未明确。我们在PTP1B启动子内鉴定出一段增强子序列,它可作为转录因子Y盒结合蛋白1(YB-1)的结合位点。YB-1的过表达导致PTP1B水平升高。此外,通过表达特定的反义构建体耗尽YB-1蛋白,导致PTP1B的表达下降约70%,但其关系最密切的同源蛋白——酪氨酸磷酸酶TCPTP的水平没有变化。反义YB-1的表达导致对胰岛素的敏感性增加,并增强了通过细胞因子受体gp130的信号传导,而PTP1B的重新表达可抑制这种信号传导。最后,我们在癌细胞系和II型糖尿病动物模型中观察到PTP1B与YB-1表达之间的相关性。我们的数据揭示了YB-1作为PTP1B表达调节因子的重要作用,并进一步强调PTP1B是胰岛素和细胞因子介导的信号转导的关键调节因子。