Shiratsuchi T, Oda K, Nishimori H, Suzuki M, Takahashi E, Tokino T, Nakamura Y
Human Genome Center, Institute of Medical Science, University of Tokyo, 4-6-1, Shirokanedai Minato-ku, Tokyo, 108-8639, Japan.
Biochem Biophys Res Commun. 1998 Oct 9;251(1):158-65. doi: 10.1006/bbrc.1998.9408.
BAI1 (brain-specific angiogenesis inhibitor 1), a p53-target gene specifically expressed in brain, encodes a seven-span transmembrane protein considered to be a member of the secretin receptor family. Using a two-hybrid system, we isolated a cDNA encoding a product that interacts with the cytoplasmic region of BAI1 and designated it BAP3 (BAI1-associated protein 3). The BAP3 product is a novel C2 domain-containing molecule with homology to Munc13 and synaptotagmin. As with Munc13, BAP3 is expressed predominantly in brain. Deletion-mutant analysis revealed that the interaction between BAI1 and BAP3 was not mediated by the C2 domains. Its predominant expression in brain and homology to Munc13 indicate that BAP3, by interacting with BAI1, might be involved in some neuronal function such as regulating release of neurotransmitters.
脑特异性血管生成抑制因子1(BAI1)是一种在脑中特异性表达的p53靶基因,它编码一种七跨膜蛋白,被认为是促胰液素受体家族的成员。利用双杂交系统,我们分离出一个编码与BAI1胞质区域相互作用产物的cDNA,并将其命名为BAP3(BAI1相关蛋白3)。BAP3产物是一种新型的含C2结构域的分子,与Munc13和突触结合蛋白具有同源性。与Munc13一样,BAP3主要在脑中表达。缺失突变分析表明,BAI1与BAP3之间的相互作用不是由C2结构域介导的。它在脑中的主要表达以及与Munc13的同源性表明,BAP3通过与BAI1相互作用,可能参与某些神经元功能,如调节神经递质的释放。