Brodie Laboratory for Craniofacial Genetics, University of Illinois at Chicago, 801 South Paulina Street, Chicago, IL 60612, USA.
Gene. 2010 Jul 15;460(1-2):8-19. doi: 10.1016/j.gene.2010.03.014. Epub 2010 Apr 11.
The cp27 gene is a highly conserved and unique gene with important roles related to craniofacial organogenesis. The present study is a first analysis of the CP27 promoter and its regulation. Here, we have cloned the promoter of the mouse cp27 gene, examined its transcriptional activity, and identified transcription factor binding sites in the proximal promoter region. Two major transcription start sites were mapped adjacent to exon 1. Promoter function analysis of the 5' flanking region by progressive 5' deletion mutations localized transcription repression elements between -1993bp and -969bp and several positive elements between -968bp and the preferred transcription start site. EMSA and functional studies indicated two function-cooperative CCAAT boxes and identified the NF-Y transcription factor as the CCAAT activator controlling transactivation of the CP27 promoter. In addition, this study demonstrated that for its effective binding and function, NF-Y required not only the minimal DNA segment length identified by deletion studies, but also a defined nucleotide sequence in the distal 3' flanking region of the CP27 proximal promoter CCAAT box. These results provide a basis for our understanding of the specific regulation of the cp27 gene in the NF-Y-mediated gene transcription network.
CP27 基因是一个高度保守且独特的基因,与颅面器官发生有重要关系。本研究首次对 CP27 启动子及其调控进行了分析。我们克隆了小鼠 cp27 基因的启动子,检测了其转录活性,并鉴定了近端启动子区域的转录因子结合位点。两个主要的转录起始位点被映射到外显子 1 附近。通过逐步 5'缺失突变对 5'侧翼区的启动子功能分析,将转录抑制元件定位在-1993bp 和-969bp 之间,以及在-968bp 和首选转录起始位点之间的几个正元件。EMSA 和功能研究表明,两个功能协同的 CCAAT 盒,并确定 NF-Y 转录因子是控制 CP27 启动子转录激活的 CCAAT 激活剂。此外,本研究表明,为了有效结合和功能,NF-Y 不仅需要由缺失研究确定的最小 DNA 片段长度,还需要 CP27 近端启动子 CCAAT 盒的远端 3'侧翼区域的特定核苷酸序列。这些结果为我们理解 NF-Y 介导的基因转录网络中 cp27 基因的特定调控提供了基础。