Funke Lars, Dakoji Srikanth, Bredt David S
Department of Physiology, University of California at San Francisco, California 94143, USA.
Annu Rev Biochem. 2005;74:219-45. doi: 10.1146/annurev.biochem.74.082803.133339.
Tissue development, differentiation, and physiology require specialized cellular adhesion and signal transduction at sites of cell-cell contact. Scaffolding proteins that tether adhesion molecules, receptors, and intracellular signaling enzymes organize macromolecular protein complexes at cellular junctions to integrate these functions. One family of such scaffolding proteins is the large group of membrane-associated guanylate kinases (MAGUKs). Genetic studies have highlighted critical roles for MAGUK proteins in the development and physiology of numerous tissues from a variety of metazoan organisms. Mutation of Drosophila discs large (dlg) disrupts epithelial septate junctions and causes overgrowth of imaginal discs. Similarly, mutation of lin-2, a related MAGUK in Caenorhabditis elegans, blocks vulval development, and mutation of the postsynaptic density protein PSD-95 impairs synaptic plasticity in mammalian brain. These diverse roles are explained by recent biochemical and structural analyses of MAGUKs, which demonstrate their capacity to assemble well--efined--yet adaptable--protein complexes at cellular junctions.
组织发育、分化和生理功能需要在细胞间接触部位进行特殊的细胞黏附与信号转导。连接黏附分子、受体和细胞内信号酶的支架蛋白在细胞连接处组织大分子蛋白复合物,以整合这些功能。这类支架蛋白的一个家族是一大类膜相关鸟苷酸激酶(MAGUKs)。遗传学研究突显了MAGUK蛋白在多种后生动物众多组织的发育和生理过程中的关键作用。果蝇盘大蛋白(dlg)的突变会破坏上皮分隔连接,并导致成虫盘过度生长。同样,秀丽隐杆线虫中相关的MAGUK蛋白lin-2的突变会阻碍外阴发育,而突触后致密蛋白PSD-95的突变会损害哺乳动物大脑中的突触可塑性。最近对MAGUKs的生化和结构分析解释了这些不同的作用,这些分析表明它们有能力在细胞连接处组装定义明确但又具有适应性的蛋白复合物。