Conkright Michael D, Guzmán Ernesto, Flechner Lawrence, Su Andrew I, Hogenesch John B, Montminy Marc
Salk Institute for Biological Studies, La Jolla, California 92037, USA.
Mol Cell. 2003 Apr;11(4):1101-8. doi: 10.1016/s1097-2765(03)00134-5.
We have employed a hidden Markov model (HMM) based on known cAMP responsive elements to search for putative CREB target genes. The best scoring sites were positionally conserved between mouse and human orthologs, suggesting that this parameter can be used to enrich for true CREB targets. Target validation experiments revealed a core promoter requirement for transcriptional induction via CREB; TATA-less promoters were unresponsive to cAMP compared to TATA-containing genes, despite comparable binding of CREB to both sets of genes in vivo. Indeed, insertion of a TATA box motif rescued cAMP responsiveness on a TATA-less promoter. These results illustrate a mechanism by which subsets of target genes for a transcription factor are differentially regulated depending on core promoter configuration.
我们利用基于已知环磷酸腺苷(cAMP)反应元件的隐马尔可夫模型(HMM)来搜索假定的CREB靶基因。得分最高的位点在小鼠和人类直系同源基因之间具有位置保守性,这表明该参数可用于富集真正的CREB靶标。靶标验证实验揭示了通过CREB进行转录诱导对核心启动子的需求;与含TATA盒的基因相比,无TATA盒的启动子对cAMP无反应,尽管CREB在体内与这两组基因的结合相当。实际上,插入TATA盒基序可挽救无TATA盒启动子上的cAMP反应性。这些结果说明了一种机制,即转录因子的靶基因子集如何根据核心启动子构型受到差异调节。