Luo X, Sawadogo M
Department of Molecular Genetics, The University of Texas M.D. Anderson Cancer Center, Houston, 77030, USA.
Mol Cell Biol. 1996 Apr;16(4):1367-75. doi: 10.1128/MCB.16.4.1367.
USF is a family of basic helix-loop transcriptional factors that recognizes DNA-binding sites similar to those of the Myc oncoproteins. Here, various functional domains in the mouse USF2 protein were identified and characterized. Indirect immunofluorescence studies with transiently transfected cells revealed that both the basic region and the highly conserved USF-specific region (USR) are involved in the nuclear localization of USF2. Cotransfection assays with deletion mutants containing the DNA-binding domain of either USF2 or GAL4 identified two distinct transcriptional activation domains in USF2, the USR and the exon 5-encoded region. Activity of the exon 5 activation domain was detectable in both assay systems. Within USF2, however, its potency varied with the conformation induced by the surrounding regions, especially that encoded by alternatively spliced exon 4. In contrast, the USR activated transcription only in its natural context upstream of the USF2 basic region and only with reporter constructs containing the adenovirus major late minimal promoter but not the E1b minimal promoter. However, insertion of an initiator element downstream of the TATA box rescued the activity of the USR on the E1b-driven reporters. The USR therefore represents a new type of activation domain whose function depends very strongly on the core promoter context.
USF是一类碱性螺旋-环转录因子家族,可识别与Myc癌蛋白类似的DNA结合位点。在此,对小鼠USF2蛋白中的各种功能结构域进行了鉴定和表征。对瞬时转染细胞进行的间接免疫荧光研究表明,碱性区域和高度保守的USF特异性区域(USR)均参与USF2的核定位。用含有USF2或GAL4 DNA结合结构域的缺失突变体进行的共转染试验,在USF2中鉴定出两个不同的转录激活结构域,即USR和外显子5编码区域。在两种检测系统中均能检测到外显子5激活结构域的活性。然而,在USF2内部,其效力随周围区域(尤其是由可变剪接的外显子4编码的区域)诱导的构象而变化。相比之下,USR仅在其位于USF2碱性区域上游的天然环境中激活转录,并且仅与含有腺病毒主要晚期最小启动子而非E1b最小启动子的报告基因构建体一起发挥作用。然而,在TATA框下游插入一个起始元件可挽救USR在E1b驱动的报告基因上的活性。因此,USR代表了一种新型的激活结构域,其功能在很大程度上取决于核心启动子环境。