Institute of Biotechnology, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan, Taiwan.
FEBS Lett. 2012 Jul 30;586(16):2260-6. doi: 10.1016/j.febslet.2012.05.059. Epub 2012 Jun 7.
In nucleus, eIF4E regulates the nucleus export of specific mRNA. In this study, altered 4E-BP3 (eIF4E-binding protein 3) expression resulted in profoundly affected cyclin D1 protein levels, partially due to changes in the cytoplasmic cyclin D1 mRNA levels in both U2OS and MCF7 cells, whereas altered 4E-BP1 expression did not affect eIF4E-mediated cyclin D1 mRNA export. 4E-BP3 also affected a subset of growth promoting mRNAs exported in an eIF4-dependent manner. Furthermore, 4E-BP3 interacted with dephosphorylated RPA2 (replication protein A2). The results indicated 4E-BP3 acts as an inhibitor of eIF4E-mediated mRNA export in the examined cells, and 4E-BP3 inhibition of eIF4E-mediated mRNA export is regulated by the phosphorylation state of RPA2.
在核内,eIF4E 调节特定 mRNA 的核输出。在这项研究中,改变 4E-BP3(eIF4E 结合蛋白 3)的表达导致细胞周期蛋白 D1 蛋白水平发生深刻变化,部分原因是 U2OS 和 MCF7 细胞中细胞质细胞周期蛋白 D1 mRNA 水平的变化,而改变 4E-BP1 的表达并不影响 eIF4E 介导的细胞周期蛋白 D1 mRNA 输出。4E-BP3 还影响了一组以 eIF4 依赖方式输出的促进生长的 mRNA。此外,4E-BP3 与去磷酸化的 RPA2(复制蛋白 A2)相互作用。结果表明,在研究的细胞中,4E-BP3 作为 eIF4E 介导的 mRNA 输出的抑制剂,而 4E-BP3 对 eIF4E 介导的 mRNA 输出的抑制作用受 RPA2 磷酸化状态的调节。