Meng J J, Bornslaeger E A, Green K J, Steinert P M, Ip W
Department of Cell Biology, Neurobiology and Anatomy, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0521, USA.
J Biol Chem. 1997 Aug 22;272(34):21495-503. doi: 10.1074/jbc.272.34.21495.
Desmosomes are cell junctions that act as sites of strong intercellular adhesion and also serve to anchor the intermediate filament (IF) cytoskeleton to the plasma membrane of a variety of cell types. Previous studies demonstrated that the COOH terminus of the desmosomal plaque protein, desmoplakin (DP), is required for the association of DP with IF networks in cultured cells and that this domain interacts directly with type II epidermal keratin polypeptides in vitro. However, these studies left open the question of how desmosomes might anchor other IF types known to associate with these junctions. In this report we used yeast two-hybrid and in vitro dot blot assays to further examine the requirements for direct interactions between desmoplakin and various IF types. Our results confirm the ability of the DP COOH terminus (DPCT) to interact with at least two regions of the head domain of the type II epidermal keratin K1 and also demonstrate that DPCT can interact with the type III IF family members, vimentin and desmin, as well as simple epithelial keratins. Unlike the situation for type II epidermal keratins, the interaction between DPCT and simple epithelial keratins appears to depend on heterodimerization of the type I and II keratin polypeptides, since both are required to detect an interaction. Furthermore, although the interaction between DPCT and K1 requires the keratin head domain, deletion of this domain from the simple epithelial keratins does not compromise interaction with DPCT. The interaction between DPCT and type III or simple epithelial keratins also appeared to be less robust than that between DPCT and K1. In the case of K8/K18, however, the interaction as assessed by yeast two-hybrid assays increased 9-fold when a serine located in a protein kinase A consensus phosphorylation site 23 residues from the end of DP was altered to a glycine. Taken together, these data indicate that DP interacts directly with different IF types in specific ways.
桥粒是一种细胞连接,它作为细胞间强黏附的位点,还能将中间丝(IF)细胞骨架锚定到多种细胞类型的质膜上。先前的研究表明,桥粒斑蛋白桥粒芯蛋白(DP)的COOH末端对于DP在培养细胞中与IF网络的结合是必需的,并且该结构域在体外可直接与II型表皮角蛋白多肽相互作用。然而,这些研究没有解决桥粒如何锚定已知与这些连接相关的其他IF类型的问题。在本报告中,我们使用酵母双杂交和体外斑点印迹分析进一步研究桥粒芯蛋白与各种IF类型之间直接相互作用的要求。我们的结果证实了DP COOH末端(DPCT)与II型表皮角蛋白K1头部结构域的至少两个区域相互作用的能力,并且还表明DPCT可以与III型IF家族成员波形蛋白和结蛋白以及简单上皮角蛋白相互作用。与II型表皮角蛋白的情况不同,DPCT与简单上皮角蛋白之间的相互作用似乎取决于I型和II型角蛋白多肽的异二聚化,因为两者都是检测相互作用所必需的。此外,尽管DPCT与K1之间的相互作用需要角蛋白头部结构域,但从简单上皮角蛋白中删除该结构域并不影响与DPCT的相互作用。DPCT与III型或简单上皮角蛋白之间的相互作用似乎也不如DPCT与K1之间的相互作用牢固。然而,在K8 / K18的情况下,当位于DP末端23个残基处的蛋白激酶A共有磷酸化位点中的丝氨酸改变为甘氨酸时,通过酵母双杂交分析评估的相互作用增加了9倍。综上所述,这些数据表明DP以特定方式直接与不同的IF类型相互作用。