Adams T E
Centre for Animal Biotechnology, University of Melbourne, Parkville, Victoria 3052, Australia.
Biochem J. 1999 Dec 15;344 Pt 3(Pt 3):867-72.
The P2 promoter of the gene for growth hormone receptor is developmentally regulated and is differentially active in a number of tissues. Little is known about the identity of the transcription factors that participate to effect this pattern of transcription. Deletion analysis and transient transfection were used to localize a previously identified cis-acting element within the sheep P2 promoter to between positions -99 and -87. Gel mobility-shift assays with nuclear extracts from Chinese hamster ovary (CHO-K1) fibroblasts revealed that this sequence encompasses an atypical binding site for both Sp1 and two isoforms of Sp3. A gel mobility-shift scan of promoter sequences between -88 and +21 indicated the existence of three other binding sites for Sp1 and Sp3. One of these, designated site II and found by using a probe spanning -74 to -54, corresponds to a classical GC box consensus sequence. Site III (-63 to -41) and site IV (-27 to -5) harbour atypical Sp1/Sp3-binding sequences. Site-directed mutagenesis of site II or site IV decreased promoter activity by approx. 40%, whereas a promoter construct incorporating both mutations exhibited negligible (approx. 1%) activity. Co-transfection of expression plasmids encoding either Sp1 or Sp3 significantly transactivated reporter gene activity from a P2 promoter construct carrying all four Sp1/Sp3-binding sites (8-fold compared with 7.1-fold induction respectively). Sp1 is known to interact with a variety of other transcription factors to regulate the transcription of a number of differentially expressed genes. The identification of four binding sites for Sp1 and Sp3 within the P2 promoter of the gene for growth hormone receptor might point to other factors that interact to regulate the activity of this promoter in different tissues during foetal and post-natal development.
生长激素受体基因的P2启动子受发育调控,在多个组织中具有不同的活性。对于参与实现这种转录模式的转录因子的身份知之甚少。通过缺失分析和瞬时转染,将先前在绵羊P2启动子中鉴定出的顺式作用元件定位在-99至-87位之间。用中国仓鼠卵巢(CHO-K1)成纤维细胞的核提取物进行凝胶迁移率变动分析表明,该序列包含Sp1和Sp3的两种同工型的非典型结合位点。对-88至+21之间的启动子序列进行凝胶迁移率变动扫描表明,还存在另外三个Sp1和Sp3的结合位点。其中一个,命名为位点II,通过使用跨越-74至-54的探针发现,对应于一个经典的GC盒共有序列。位点III(-63至-41)和位点IV(-27至-5)含有非典型的Sp1/Sp3结合序列。对位点II或位点IV进行定点诱变可使启动子活性降低约40%,而包含这两种突变的启动子构建体的活性可忽略不计(约1%)。共转染编码Sp1或Sp3的表达质粒可显著激活携带所有四个Sp1/Sp3结合位点的P2启动子构建体的报告基因活性(分别为8倍和7.1倍诱导)。已知Sp1与多种其他转录因子相互作用,以调节许多差异表达基因的转录。在生长激素受体基因的P2启动子中鉴定出四个Sp1和Sp3的结合位点,这可能指向在胎儿期和出生后发育过程中相互作用以调节该启动子在不同组织中活性的其他因子。