Goding C R, Temperley S M, Fisher F
Marie Curie Research Institute, Oxted, Surrey, UK.
Nucleic Acids Res. 1987 Oct 12;15(19):7761-80. doi: 10.1093/nar/15.19.7761.
Multiple cellular transcription factors have been shown to interact with the upstream region of the adenovirus-2 EIIa-late promoter. One of these factors recognises each of the three CCAAT motifs present in the EIIL promoter at positions -72, -135 and -229, as well as the CCAAT elements in the rat albumin and herpes virus thymidine kinase promoters. A mutation known to reduce thymidine kinase promoter activity in vivo and in vitro abolishes binding of the factor, termed CCAAT recognition factor (CRF), which appears to be distinct from previously identified CCAAT factors. In addition, another protein, termed upstream factor II (USFII), shares binding sites at position -110 in the EIIL promoter and in the c-fos enhancer adjacent to the serum regulatable element. The recognition site for USFII is also found in the c-fos promoter and in the adenovirus early region EIV and EIIa-early promoters. An Sp1 recognition site has also been identified at position -41, and the binding sites for Sp1, USFII and CRF are all required for efficient EIIa-late promoter function. Finally, an additional factor recognising the consensus GGGGGGNT has been detected.
已证明多种细胞转录因子可与腺病毒2型EIIa晚期启动子的上游区域相互作用。其中一种因子可识别EIIL启动子中位于-72、-135和-229位置的三个CCAAT基序,以及大鼠白蛋白和疱疹病毒胸苷激酶启动子中的CCAAT元件。一种已知在体内和体外均可降低胸苷激酶启动子活性的突变会消除该因子(称为CCAAT识别因子(CRF))的结合,该因子似乎与先前鉴定的CCAAT因子不同。此外,另一种蛋白质,称为上游因子II(USFII),在EIIL启动子中-110位置以及与血清可调节元件相邻的c-fos增强子中共享结合位点。在c-fos启动子以及腺病毒早期区域EIV和EIIa早期启动子中也发现了USFII的识别位点。在-41位置还鉴定出一个Sp1识别位点,高效的EIIa晚期启动子功能需要Sp1、USFII和CRF的结合位点。最后,检测到另一种识别共有序列GGGGGGNT的因子。