Somma M P, Gambino I, Lavia P
Centro di Genetica Evoluzionistica del CNR, Rome, Italy.
Nucleic Acids Res. 1991 Aug 25;19(16):4451-8. doi: 10.1093/nar/19.16.4451.
The mouse CpG island HTF9 harbours a bidirectional promoter shared by two housekeeping genes that are arranged head-to-head. We have previously identified several protein binding-elements across the CpG island, yet a short region around the initiation region was found to be capable of bidirectional transcription in transient expression assays, suggesting that the multiple elements of the HTF9 promoter are functionally redundant. We have now compared the binding activities in nuclear extracts from different cell types. Two protein-binding elements of HTF9 interact with widely distributed factors. A potentially strong Sp1 binding site was also identified, however Sp1 appeared to bind efficiently to its target sequence with extracts prepared from proliferating cultured cells, but not from adult organs. On the other hand, the CCAAT box upstream of one gene (HTF9-A) interacted with a liver-enriched factor, whereas no binding was detected with cultured fibroblasts extracts. Consistently, deletion of the CCAAT box affected transient expression from the HTF9-A promoter in hepatocyte, but not in fibroblast, cultures. Our results suggest that ubiquitous expression of housekeeping promoters results from the activation of alternative elements in different cell types.
小鼠CpG岛HTF9含有一个由两个管家基因共享的双向启动子,这两个基因呈头对头排列。我们之前已经在整个CpG岛上鉴定出了几个蛋白质结合元件,然而,在瞬时表达实验中发现起始区域周围的一个短区域能够进行双向转录,这表明HTF9启动子的多个元件在功能上是冗余的。我们现在比较了不同细胞类型核提取物中的结合活性。HTF9的两个蛋白质结合元件与广泛分布的因子相互作用。还鉴定出了一个潜在的强Sp1结合位点,然而,Sp1似乎能有效地与其靶序列结合,该靶序列存在于增殖培养细胞制备的提取物中,但不存在于成年器官制备的提取物中。另一方面,一个基因(HTF9-A)上游的CCAAT框与一种肝脏富集因子相互作用,而在培养的成纤维细胞提取物中未检测到结合。一致的是,删除CCAAT框会影响肝细胞培养中HTF9-A启动子的瞬时表达,但不影响成纤维细胞培养中的表达。我们的结果表明,管家启动子的普遍表达是由不同细胞类型中替代元件的激活引起的。