Ahn S, Olive M, Aggarwal S, Krylov D, Ginty D D, Vinson C
Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Mol Cell Biol. 1998 Feb;18(2):967-77. doi: 10.1128/MCB.18.2.967.
Several studies have characterized the upstream regulatory region of c-fos, and identified cis-acting elements termed the cyclic AMP (cAMP) response elements (CREs) that are critical for c-fos transcription in response to a variety of extracellular stimuli. Although several transcription factors can bind to CREs in vitro, the identity of the transcription factor(s) that activates the c-fos promoter via the CRE in vivo remains unclear. To help identify the trans-acting factors that regulate stimulus-dependent transcription of c-fos via the CREs, dominant-negative (D-N) inhibitor proteins that function by preventing DNA binding of B-ZIP proteins in a dimerization domain-dependent fashion were developed. A D-N inhibitor of CREB, termed A-CREB, was constructed by fusing a designed acidic amphipathic extension onto the N terminus of the CREB leucine zipper domain. The acidic extension of A-CREB interacts with the basic region of CREB forming a coiled-coil extension of the leucine zipper and thus prevents the basic region of wild-type CREB from binding to DNA. Other D-N inhibitors generated in a similar manner with the dimerization domains of Fos, Jun, C/EBP, ATF-2, or VBP did not block CREB DNA binding activity, nor did they inhibit transcriptional activation of a minimal promoter containing a single CRE in PC12 cells. A-CREB inhibited activation of CRE-mediated transcription evoked by three distinct stimuli: forskolin, which increases intracellular cAMP; membrane depolarization, which promotes Ca2+ influx; and nerve growth factor (NGF). A-CREB completely inhibited cAMP-mediated, but only partially inhibited Ca2+- and NGF-mediated, transcription of a reporter gene containing 750 bp of the native c-fos promoter. Moreover, glutamate induction of c-fos expression in primary cortical neurons was dependent on CREB. In contrast, induction of c-fos transcription by UV light was not inhibited by A-CREB. Lastly, A-CREB attenuated NGF induction of morphological differentiation in PC12 cells. These results suggest that CREB or its closely related family members are general mediators of stimulus-dependent transcription of c-fos and are required for at least some of the long-term actions of NGF.
多项研究已对c-fos的上游调控区域进行了表征,并鉴定出了顺式作用元件,即环磷酸腺苷(cAMP)反应元件(CREs),这些元件对于c-fos在响应多种细胞外刺激时的转录至关重要。尽管有几种转录因子在体外可与CREs结合,但在体内通过CRE激活c-fos启动子的转录因子的身份仍不清楚。为了帮助鉴定通过CREs调节c-fos刺激依赖性转录的反式作用因子,开发了显性负性(D-N)抑制蛋白,其通过以二聚化结构域依赖性方式阻止B-ZIP蛋白与DNA结合来发挥作用。一种称为A-CREB的CREB的D-N抑制剂,是通过将设计的酸性两亲性延伸融合到CREB亮氨酸拉链结构域的N末端构建而成的。A-CREB的酸性延伸与CREB的碱性区域相互作用,形成亮氨酸拉链的卷曲螺旋延伸,从而阻止野生型CREB的碱性区域与DNA结合。以类似方式与Fos、Jun、C/EBP、ATF-2或VBP的二聚化结构域产生的其他D-N抑制剂并未阻断CREB的DNA结合活性,它们也未抑制PC12细胞中含有单个CRE的最小启动子的转录激活。A-CREB抑制了由三种不同刺激引起的CRE介导的转录激活:可增加细胞内cAMP的福斯可林;促进Ca2+内流的膜去极化;以及神经生长因子(NGF)。A-CREB完全抑制了cAMP介导的转录,但仅部分抑制了Ca2+和NGF介导的、含有750 bp天然c-fos启动子的报告基因的转录。此外,原代皮质神经元中谷氨酸诱导的c-fos表达依赖于CREB。相反,紫外线诱导的c-fos转录不受A-CREB的抑制。最后,A-CREB减弱了PC12细胞中NGF诱导的形态分化。这些结果表明,CREB或其密切相关的家族成员是c-fos刺激依赖性转录的一般介质,并且是NGF至少一些长期作用所必需的。