Kim Mi-Young, Ahn Kyu Youn, Lee Seon Min, Koh Jeong Tae, Chun Byeong Jo, Bae Choon Sang, Lee Kee Sook, Kim Kyung Keun
Medical Research Center for Gene Regulation, Chonnam National University Medical School, Hak-Dong 5, Dong-Ku, Kwangju 501-190, South Korea.
FEBS Lett. 2004 May 21;566(1-3):87-94. doi: 10.1016/j.febslet.2004.03.106.
Restricting transgene expression to specific cell types and maintaining long-term expression are major goals for gene therapy. Previously, we cloned brain-specific angiogenesis inhibitor 1-associated protein 4 (BAI1-AP4), a novel brain-specific protein that interacts with BAI1, and found that it was developmentally upregulated in the adult brain. In this report, we isolated 5 kb of the 5' upstream sequence of the mouse BAI1-AP4 gene and analyzed its promoter activity. Functional analyses demonstrated that an Sp1 site was the enhancer, and the region containing the transcription initiation site and an AP2-binding site was the basal promoter. We examined the ability of the BAI1-AP4 promoter to drive adult brain-specific expression by using it to drive lacZ expression in transgenic (TG) mice. Northern blot analyses showed a unique pattern of beta-galactosidase expression in TG brain, peaking at 1 month after birth, like endogenous BAI1-AP4. Histological analyses demonstrated the same localization and developmental expression of beta-galactosidase and BAI1-AP4 in most neurons of the cerebral cortex and hippocampus. Our data indicate that TG mice carrying the BAI1-AP4 promoter could be a valuable model system for region-specific brain diseases.
将转基因表达限制在特定细胞类型并维持长期表达是基因治疗的主要目标。此前,我们克隆了脑特异性血管生成抑制因子1相关蛋白4(BAI1-AP4),一种与BAI1相互作用的新型脑特异性蛋白,并发现其在成年大脑中发育性上调。在本报告中,我们分离了小鼠BAI1-AP4基因5'上游序列的5 kb,并分析了其启动子活性。功能分析表明,一个Sp1位点是增强子,包含转录起始位点和一个AP2结合位点的区域是基础启动子。我们通过在转基因(TG)小鼠中利用BAI1-AP4启动子驱动lacZ表达,研究了其驱动成年脑特异性表达的能力。Northern印迹分析显示,TG脑中β-半乳糖苷酶表达具有独特模式,在出生后1个月达到峰值,与内源性BAI1-AP4相似。组织学分析表明,β-半乳糖苷酶和BAI1-AP4在大脑皮层和海马体的大多数神经元中具有相同的定位和发育表达。我们的数据表明,携带BAI1-AP4启动子的TG小鼠可能是用于区域特异性脑部疾病的有价值的模型系统。