Amelio Antonio L, Caputi Massimo, Conkright Michael D
Department of Cancer Biology, The Scripps Research Institute, Scripps Florida, Jupiter, FL 33458, USA.
EMBO J. 2009 Sep 16;28(18):2733-47. doi: 10.1038/emboj.2009.216. Epub 2009 Jul 30.
The CREB regulated transcription co-activators (CRTCs) regulate many biological processes by integrating and converting environmental inputs into transcriptional responses. Although the mechanisms by which CRTCs sense cellular signals are characterized, little is known regarding how CRTCs contribute to the regulation of cAMP inducible genes. Here we show that these dynamic regulators, unlike other co-activators, independently direct either pre-mRNA splice-site selection or transcriptional activation depending on the cell type or promoter context. Moreover, in other scenarios, the CRTC co-activators coordinately regulate transcription and splicing. Mutational analyses showed that CRTCs possess distinct functional domains responsible for regulating either pre-mRNA splicing or transcriptional activation. Interestingly, the CRTC1-MAML2 oncoprotein lacks the splicing domain and is incapable of altering splice-site selection despite robustly activating transcription. The differential usage of these distinct domains allows CRTCs to selectively mediate multiple facets of gene regulation, indicating that co-activators are not solely restricted to coordinating alternative splicing with increase in transcriptional activity.
CREB调节转录共激活因子(CRTCs)通过整合环境输入信号并将其转化为转录反应来调节许多生物学过程。尽管CRTCs感知细胞信号的机制已得到表征,但关于CRTCs如何参与cAMP诱导基因的调节知之甚少。在此我们表明,与其他共激活因子不同,这些动态调节因子根据细胞类型或启动子背景独立地指导前体mRNA剪接位点选择或转录激活。此外,在其他情况下,CRTC共激活因子协同调节转录和剪接。突变分析表明,CRTCs具有负责调节前体mRNA剪接或转录激活的不同功能域。有趣的是,CRTC1-MAML2癌蛋白缺乏剪接结构域,尽管能强烈激活转录,但无法改变剪接位点选择。这些不同结构域的差异使用使CRTCs能够选择性地介导基因调节的多个方面,表明共激活因子不仅限于通过增加转录活性来协调可变剪接。