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© The Rockefeller University Press, 0021-9525/1998//1229 $5.00
The Journal of Cell Biology, Volume 141, Number 5, , 1998 1229-1241

Articles

Defining the Interactions Between Intermediate Filaments and Desmosomes



Elizabeth A. Smith{ddagger} and Elaine Fuchs*

Howard Hughes Medical Institute, * Department of Molecular Genetics and Cell Biology and {ddagger} Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, Illinois 60637

Desmoplakin (DP), plakoglobin (PG), and plakophilin 1 (PP1) are desmosomal components lacking a transmembrane domain, thus making them candidate linker proteins for connecting intermediate filaments and desmosomes. Using deletion and site-directed mutagenesis, we show that remarkably, removal of ~1% of DP's sequence obliterates its ability to associate with desmosomes. Conversely, when linked to a foreign protein, as few as 86 NH2-terminal DP residues are sufficient to target to desmosomes efficiently. In in vitro overlay assays, the DP head specifically associates with itself and with desmocollin 1a (Dsc1a). In similar overlay assays, PP1 binds to DP and Dsc1a, and to a lesser extent, desmoglein 1 (Dsg1), while PG binds to Dsg1 and more weakly to Dsc1a and DP. Interestingly, like DP, PG and PP1 associate with epidermal keratins, although PG is considerably weaker in its ability to do so. As judged by overlay assays, the amino terminal head domain of type II keratins appears to have a special importance in establishing these connections. Taken together, our findings provide new insights into the complexities of the links between desmosomes and intermediate filaments (IFs). Our results suggest a model whereby at desmosome sites within dividing epidermal cells, DP and PG anchor to desmosomal cadherins and to each other, forming an ordered array of nontransmembrane proteins that then bind to keratin IFs. As epidermal cells differentiate, PP1 is added as a molecular reinforcement to the plaque, enhancing anchorage to IFs and accounting at least partially for the increase in numbers and stability of desmosomes in suprabasal cells.

Abbreviations used in this paper: aa, amino acids; BPAGIe, epidermal bullous pemphigoid antigen 1 protein; DPH, desmoplakin; DP, desmoplakin; Dscs, desmocollins; Dsgs, desmogleins; IFs, intermediate filaments; PG, plakoglobin; PP1, plakophilin 1.

E.F. is an Investigator of the Howard Hughes Medical Institute.


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