Lai W S, Thompson M J, Taylor G A, Liu Y, Blackshear P J
Howard Hughes Medical Institute Laboratories, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Biol Chem. 1995 Oct 20;270(42):25266-72. doi: 10.1074/jbc.270.42.25266.
The gene encoding the putative zinc finger protein tristetraprolin (TTP), Zfp-36, is rapidly induced by a variety of mitogens and growth factors. We show here that 77 base pairs 5' of the transcription start site are sufficient for full serum inducibility of the mouse Zfp-36 promoter. This region of the promoter includes consensus sequences for the binding of the transcription factors EGR-1, AP2, and Sp1. In addition, we have identified a previously undescribed element, TTP promoter element 1 (TPE1); this 10-base pair sequence includes a palindrome and is identical in the human, bovine, and mouse genes. Each of the three binding elements, EGR-1, AP2, and TPE1, contribute to the serum induction of Zfp-36 and can confer serum-inducible expression on a heterologous minimal promoter. Gel mobility shift assays demonstrated the formation of complexes consisting of this region of the promoter and cellular nuclear proteins and demonstrated that the extent of complex formation could be altered by treatment of the cells with serum or insulin. These results suggest that the response of Zfp-36 to serum and other mitogens is mediated by a series of cis-acting elements acting in concert to confer full inducible transcription of this gene.
编码假定锌指蛋白Tristetraprolin(TTP,即Zfp-36)的基因可被多种促有丝分裂原和生长因子迅速诱导。我们在此表明,转录起始位点上游5'端的77个碱基对足以使小鼠Zfp-36启动子具有完全的血清诱导性。该启动子区域包含转录因子EGR-1、AP2和Sp1结合的共有序列。此外,我们还鉴定出一个以前未描述的元件,即TTP启动子元件1(TPE1);这个10个碱基对的序列包含一个回文结构,在人、牛和小鼠基因中是相同的。EGR-1、AP2和TPE1这三个结合元件中的每一个都对Zfp-36的血清诱导有贡献,并且可以赋予异源最小启动子血清诱导性表达。凝胶迁移率变动分析证明了由启动子的这个区域和细胞核蛋白组成的复合物的形成,并证明通过用血清或胰岛素处理细胞可以改变复合物形成的程度。这些结果表明,Zfp-36对血清和其他促有丝分裂原的反应是由一系列顺式作用元件协同作用介导的,从而赋予该基因完全的诱导性转录。