Skip to main content

Advertisement

Log in

Epidermal cell junctions and their regulation by p63 in health and disease

  • Review
  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Abstract

As the outermost tissue of the body, the epidermis is the first physical barrier for any pressure, stress or trauma. Several specialized cell–matrix and cell–cell adhesion structures, together with an intracellular network of dedicated intermediate filaments, are required to confer critical resilience to mechanical stress. The transcription factor p63 is a master regulator of gene expression in the epidermis and in other stratified epithelia. It has been extensively demonstrated that p63 positively controls a large number of tissue-specific genes, including those encoding a large fraction of tissue-restricted cell adhesion molecules. Consistent with p63 functions in cell adhesion and in epidermal differentiation, heterozygous mutations clustered mainly in the p63 C-terminus are causative of AEC syndrome, an autosomal dominant disorder characterized by cleft palate, ankyloblepharon and ectodermal dysplasia associated with severe skin erosions, bleeding and infections. The molecular basis of skin erosions in AEC patients is not fully understood, although defects in desmosomes and in other cell junctions are likely to be involved. Here, we provide an extensive review of the different epidermal cell junctions that cooperate to withstand mechanical stress and on the mechanisms by which p63 regulates gene expression of their components in healthy skin and in AEC syndrome. Collectively, advancement in understanding the molecular mechanisms by which epidermal cell junctions precisely exert their functions and how p63 orchestrates their coordinated expression, will ultimately lead to insight into developing future strategies for the treatment of AEC syndrome and more in generally for diseases that share an overlapping phenotype.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  • Amagai M, Stanley JR (2012) Desmoglein as a target in skin disease and beyond. J Invest Dermatol 132:776–784

    PubMed Central  CAS  PubMed  Google Scholar 

  • Andra K, Lassmann H, Bittner R, Shorny S, Fassler R, Propst F, Wiche G (1997) Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture. Genes Dev 11:3143–3156

    PubMed Central  CAS  PubMed  Google Scholar 

  • Antonini D, Rossi B, Han R, Minichiello A, Di Palma T, Corrado M, Banfi S, Zannini M, Brissette JL, Missero C (2006) An autoregulatory loop directs the tissue-specific expression of p63 through a long-range evolutionarily conserved enhancer. Mol Cell Biol 26:3308–3318

    PubMed Central  CAS  PubMed  Google Scholar 

  • Armstrong DK, McKenna KE, Purkis PE, Green KJ, Eady RA, Leigh IM, Hughes AE (1999) Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma. Hum Mol Genet 8:143–148

    CAS  PubMed  Google Scholar 

  • Ayub M, Basit S, Jelani M, Ur Rehman F, Iqbal M, Yasinzai M, Ahmad W (2009) A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles. Am J Hum Genet 85:515–520

    PubMed Central  CAS  PubMed  Google Scholar 

  • Barron MJ, Brookes SJ, Draper CE, Garrod D, Kirkham J, Shore RC, Dixon MJ (2008) The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice. Hum Mol Genet 17:3509–3520

    PubMed Central  CAS  PubMed  Google Scholar 

  • Bass-Zubek AE, Hobbs RP, Amargo EV, Garcia NJ, Hsieh SN, Chen X, Wahl JK 3rd, Denning MF, Green KJ (2008) Plakophilin 2: a critical scaffold for PKC alpha that regulates intercellular junction assembly. J Cell Biol 181:605–613

    PubMed Central  CAS  PubMed  Google Scholar 

  • Beaudry VG, Pathak N, Koster MI, Attardi LD (2009) Differential PERP regulation by TP63 mutants provides insight into AEC pathogenesis. Am J Med Genet A 149A:1952–1957

    CAS  PubMed  Google Scholar 

  • Berx G, van Roy F (2009) Involvement of members of the cadherin superfamily in cancer. Cold Spring Harb Perspect Biol 1:a003129

    PubMed Central  PubMed  Google Scholar 

  • Bonifas JM, Rothman AL, Epstein EH Jr (1991) Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities. Science 254:1202–1205

    CAS  PubMed  Google Scholar 

  • Bouchard MJ, Dong Y, McDermott BM Jr, Lam DH, Brown KR, Shelanski M, Bellve AR, Racaniello VR (2000) Defects in nuclear and cytoskeletal morphology and mitochondrial localization in spermatozoa of mice lacking nectin-2, a component of cell-cell adherens junctions. Mol Cell Biol 20:2865–2873

    PubMed Central  CAS  PubMed  Google Scholar 

  • Brancati F, Fortugno P, Bottillo I, Lopez M, Josselin E, Boudghene-Stambouli O, Agolini E, Bernardini L, Bellacchio E, Iannicelli M et al (2010) Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. Am J Hum Genet 87:265–273

    PubMed Central  CAS  PubMed  Google Scholar 

  • Brandner JM, Haftek M, Niessen CM (2010) Adherens junctions, desmosomes and tight junctions in epidermal barrier function. Open Dermatol J 4:14–20

  • Brasch J, Harrison OJ, Honig B, Shapiro L (2012) Thinking outside the cell: how cadherins drive adhesion. Trends Cell Biol 22:299–310

    PubMed Central  CAS  PubMed  Google Scholar 

  • Carroll DK, Carroll JS, Leong CO, Cheng F, Brown M, Mills AA, Brugge JS, Ellisen LW (2006) p63 regulates an adhesion programme and cell survival in epithelial cells. Nat Cell Biol 8:551–561

    CAS  PubMed  Google Scholar 

  • Chan YM, Yu QC, Fine JD, Fuchs E (1993) The genetic basis of Weber-Cockayne epidermolysis bullosa simplex. Proc Natl Acad Sci U S A 90:7414–7418

    PubMed Central  CAS  PubMed  Google Scholar 

  • Chen J, Den Z, Koch PJ (2008) Loss of desmocollin 3 in mice leads to epidermal blistering. J Cell Sci 121:2844–2849

    PubMed Central  CAS  PubMed  Google Scholar 

  • Chidgey M, Brakebusch C, Gustafsson E, Cruchley A, Hail C, Kirk S, Merritt A, North A, Tselepis C, Hewitt J et al (2001) Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation. J Cell Biol 155:821–832

    PubMed Central  CAS  PubMed  Google Scholar 

  • Christiano AM, Greenspan DS, Hoffman GG, Zhang X, Tamai Y, Lin AN, Dietz HC, Hovnanian A, Uitto J (1993) A missense mutation in type VII collagen in two affected siblings with recessive dystrophic epidermolysis bullosa. Nat Genet 4:62–66

    CAS  PubMed  Google Scholar 

  • Clements SE, Techanukul T, Lai-Cheong JE, Mee JB, South AP, Pourreyron C, Burrows NP, Mellerio JE, McGrath JA (2012) Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology. Br J Dermatol 167:134–144

    CAS  PubMed  Google Scholar 

  • Coulombe PA, Hutton ME, Letai A, Hebert A, Paller AS, Fuchs E (1991) Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses. Cell 66:1301–1311

    CAS  PubMed  Google Scholar 

  • De Rosa L, Antonini D, Ferone G, Russo MT, Yu PB, Han R, Missero C (2009) p63 Suppresses non-epidermal lineage markers in a bone morphogenetic protein-dependent manner via repression of Smad7. J Biol Chem 284:30574–30582

    PubMed Central  PubMed  Google Scholar 

  • Della Gatta G, Bansal M, Ambesi-Impiombato A, Antonini D, Missero C, di Bernardo D (2008) Direct targets of the TRP63 transcription factor revealed by a combination of gene expression profiling and reverse engineering. Genome Res 18:939–948

    PubMed Central  CAS  PubMed  Google Scholar 

  • Deutsch GB, Zielonka EM, Coutandin D, Weber TA, Schafer B, Hannewald J, Luh LM, Durst FG, Ibrahim M, Hoffmann J et al (2011) DNA damage in oocytes induces a switch of the quality control factor TAp63alpha from dimer to tetramer. Cell 144:566–576

    PubMed Central  CAS  PubMed  Google Scholar 

  • DiPersio CM, Hodivala-Dilke KM, Jaenisch R, Kreidberg JA, Hynes RO (1997) alpha3beta1 Integrin is required for normal development of the epidermal basement membrane. J Cell Biol 137:729–742

    PubMed Central  CAS  PubMed  Google Scholar 

  • Dishop MK, Bree AF, Hicks MJ (2009) Pathologic changes of skin and hair in ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome. Am J Med Genet A 149A:1935–1941

    PubMed  Google Scholar 

  • Dohn M, Zhang S, Chen X (2001) p63alpha and DeltaNp63alpha can induce cell cycle arrest and apoptosis and differentially regulate p53 target genes. Oncogene 20:3193–3205

    CAS  PubMed  Google Scholar 

  • Dowling J, Yu QC, Fuchs E (1996) Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival. J Cell Biol 134:559–572

    CAS  PubMed  Google Scholar 

  • Durbeej M (2010) Laminins. Cell Tissue Res 339:259–268

    CAS  PubMed  Google Scholar 

  • Feldmeyer L, Huber M, Fellmann F, Beckmann JS, Frenk E, Hohl D (2006) Confirmation of the origin of NISCH syndrome. Hum Mutat 27:408–410

    CAS  PubMed  Google Scholar 

  • Ferone G, Thomason HA, Antonini D, De Rosa L, Hu B, Gemei M, Zhou H, Ambrosio R, Rice DP, Acampora D et al (2012) Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndrome. EMBO Mol Med 4:192–205

    PubMed Central  CAS  PubMed  Google Scholar 

  • Ferone G, Mollo MR, Thomason HA, Antonini D, Zhou H, Ambrosio R, De Rosa L, Salvatore D, Getsios S, van Bokhoven H et al (2013) p63 control of desmosome gene expression and adhesion is compromised in AEC syndrome. Hum Mol Genet 22:531–543

    PubMed Central  CAS  PubMed  Google Scholar 

  • Fine JD, Bruckner-Tuderman L, Eady RA, Bauer EA, Bauer JW, Has C, Heagerty A, Hintner H, Hovnanian A, Jonkman MF et al (2014) Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. J Am Acad Dermatol 70:1103–1126

    PubMed  Google Scholar 

  • Fortugno P, Josselin E, Tsiakas K, Agolini E, Cestra G, Teson M, Santer R, Castiglia D, Novelli G, Dallapiccola B et al (2014) Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formation. J Invest Dermatol 134:2146–2153

    CAS  PubMed  Google Scholar 

  • Furuse M, Hata M, Furuse K, Yoshida Y, Haratake A, Sugitani Y, Noda T, Kubo A, Tsukita S (2002) Claudin-based tight junctions are crucial for the mammalian epidermal barrier: a lesson from claudin-1-deficient mice. J Cell Biol 156:1099–1111

    PubMed Central  CAS  PubMed  Google Scholar 

  • Gache Y, Chavanas S, Lacour JP, Wiche G, Owaribe K, Meneguzzi G, Ortonne JP (1996) Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy. J Clin Invest 97:2289–2298

    PubMed Central  CAS  PubMed  Google Scholar 

  • Georges-Labouesse E, Messaddeq N, Yehia G, Cadalbert L, Dierich A, Le Meur M (1996) Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice. Nat Genet 13:370–373

    CAS  PubMed  Google Scholar 

  • Getsios S, Huen AC, Green KJ (2004) Working out the strength and flexibility of desmosomes. Nat Rev Mol Cell Biol 5:271–281

    CAS  PubMed  Google Scholar 

  • Ghioni P, Bolognese F, Duijf PH, Van Bokhoven H, Mantovani R, Guerrini L (2002) Complex transcriptional effects of p63 isoforms: identification of novel activation and repression domains. Mol Cell Biol 22:8659–8668

    PubMed Central  CAS  PubMed  Google Scholar 

  • Gonfloni S, Di Tella L, Caldarola S, Cannata SM, Klinger FG, Di Bartolomeo C, Mattei M, Candi E, De Felici M, Melino G et al (2009) Inhibition of the c-Abl-TAp63 pathway protects mouse oocytes from chemotherapy-induced death. Nat Med 15:1179–1185

    CAS  PubMed  Google Scholar 

  • Groves RW, Liu L, Dopping-Hepenstal PJ, Markus HS, Lovell PA, Ozoemena L, Lai-Cheong JE, Gawler J, Owaribe K, Hashimoto T et al (2010) A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplex. J Invest Dermatol 130:1551–1557

    CAS  PubMed  Google Scholar 

  • Gumbiner BM (2005) Regulation of cadherin-mediated adhesion in morphogenesis. Nat Rev Mol Cell Biol 6:622–634

    CAS  PubMed  Google Scholar 

  • Guo L, Degenstein L, Dowling J, Yu QC, Wollmann R, Perman B, Fuchs E (1995) Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration. Cell 81:233–243

    CAS  PubMed  Google Scholar 

  • Guo X, Keyes WM, Papazoglu C, Zuber J, Li W, Lowe SW, Vogel H, Mills AA (2009) TAp63 induces senescence and suppresses tumorigenesis in vivo. Nat Cell Biol 11:1451–1457

    PubMed Central  CAS  PubMed  Google Scholar 

  • Hadj-Rabia S, Baala L, Vabres P, Hamel-Teillac D, Jacquemin E, Fabre M, Lyonnet S, De Prost Y, Munnich A, Hadchouel M et al (2004) Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: a tight junction disease. Gastroenterology 127:1386–1390

    CAS  PubMed  Google Scholar 

  • Halbleib JM, Nelson WJ (2006) Cadherins in development: cell adhesion, sorting, and tissue morphogenesis. Genes Dev 20:3199–3214

    CAS  PubMed  Google Scholar 

  • Has C, Sparta G, Kiritsi D, Weibel L, Moeller A, Vega-Warner V, Waters A, He Y, Anikster Y, Esser P et al (2012) Integrin alpha3 mutations with kidney, lung, and skin disease. N Engl J Med 366:1508–1514

    PubMed Central  CAS  PubMed  Google Scholar 

  • Hay RJ, Wells RS (1976) The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition. Br J Dermatol 94:277–289

    CAS  PubMed  Google Scholar 

  • Helton ES, Zhu J, Chen X (2006) The unique NH2-terminally deleted (DeltaN) residues, the PXXP motif, and the PPXY motif are required for the transcriptional activity of the DeltaN variant of p63. J Biol Chem 281:2533–2542

    CAS  PubMed  Google Scholar 

  • Hilal L, Rochat A, Duquesnoy P, Blanchet-Bardon C, Wechsler J, Martin N, Christiano AM, Barrandon Y, Uitto J, Goossens M et al (1993) A homozygous insertion-deletion in the type VII collagen gene (COL7A1) in Hallopeau-Siemens dystrophic epidermolysis bullosa. Nat Genet 5:287–293

    CAS  PubMed  Google Scholar 

  • Hobbs RP, Amargo EV, Somasundaram A, Simpson CL, Prakriya M, Denning MF, Green KJ (2011) The calcium ATPase SERCA2 regulates desmoplakin dynamics and intercellular adhesive strength through modulation of PKCα signaling. FASEB J 25:990–1001

    PubMed Central  CAS  PubMed  Google Scholar 

  • Hovnanian A, Pollack E, Hilal L, Rochat A, Prost C, Barrandon Y, Goossens M (1993) A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex. Nat Genet 3:327–332

    CAS  PubMed  Google Scholar 

  • Huelsken J, Vogel R, Erdmann B, Cotsarelis G, Birchmeier W (2001) beta-Catenin controls hair follicle morphogenesis and stem cell differentiation in the skin. Cell 105:533–545

    CAS  PubMed  Google Scholar 

  • Ihrie RA, Marques MR, Nguyen BT, Horner JS, Papazoglu C, Bronson RT, Mills AA, Attardi LD (2005) Perp is a p63-regulated gene essential for epithelial integrity. Cell 120:843–856

    CAS  PubMed  Google Scholar 

  • Ihrie RA, Bronson RT, Attardi LD (2006) Adult mice lacking the p53/p63 target gene Perp are not predisposed to spontaneous tumorigenesis but display features of ectodermal dysplasia syndromes. Cell Death Differ 13:1614–1618

    CAS  PubMed  Google Scholar 

  • Ikeda W, Nakanishi H, Miyoshi J, Mandai K, Ishizaki H, Tanaka M, Togawa A, Takahashi K, Nishioka H, Yoshida H et al (1999) Afadin: a key molecule essential for structural organization of cell-cell junctions of polarized epithelia during embryogenesis. J Cell Biol 146:1117–1132

    PubMed Central  CAS  PubMed  Google Scholar 

  • Inagaki M, Irie K, Ishizaki H, Tanaka-Okamoto M, Morimoto K, Inoue E, Ohtsuka T, Miyoshi J, Takai Y (2005) Roles of cell-adhesion molecules nectin 1 and nectin 3 in ciliary body development. Development 132:1525–1537

    CAS  PubMed  Google Scholar 

  • Ioannides D, Hytiroglou P, Phelps RG, Bystryn JC (1991) Regional variation in the expression of pemphigus foliaceus, pemphigus erythematosus, and pemphigus vulgaris antigens in human skin. J Invest Dermatol 96:159–161

    CAS  PubMed  Google Scholar 

  • Jelani M, Chishti MS, Ahmad W (2011) Mutation in PVRL4 gene encoding nectin-4 underlies ectodermal-dysplasia-syndactyly syndrome (EDSS1). J Hum Genet 56:352–357

    CAS  PubMed  Google Scholar 

  • Johnson JL, Koetsier JL, Sirico A, Agidi AT, Antonini D, Missero C, Green KJ (2014) The desmosomal protein desmoglein 1 aids recovery of epidermal differentiation after acute UV light exposure. J Invest Dermatol 134:2154–2162

    PubMed Central  CAS  PubMed  Google Scholar 

  • Jonca N, Guerrin M, Hadjiolova K, Caubet C, Gallinaro H, Simon M, Serre G (2002) Corneodesmosin, a component of epidermal corneocyte desmosomes, displays homophilic adhesive properties. J Biol Chem 277:5024–5029

    CAS  PubMed  Google Scholar 

  • Jones PH, Watt FM (1993) Separation of human epidermal stem cells from transit amplifying cells on the basis of differences in integrin function and expression. Cell 73:713–724

    CAS  PubMed  Google Scholar 

  • Jonkman MF, de Jong MC, Heeres K, Pas HH, van der Meer JB, Owaribe K, Martinez de Velasco AM, Niessen CM, Sonnenberg A (1995) 180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa. J Clin Invest 95:1345–1352

    PubMed Central  CAS  PubMed  Google Scholar 

  • Jonkman MF, Pasmooij AM, Pasmans SG, van den Berg MP, Ter Horst HJ, Timmer A, Pas HH (2005) Loss of desmoplakin tail causes lethal acantholytic epidermolysis bullosa. Am J Hum Genet 77:653–660

    PubMed Central  CAS  PubMed  Google Scholar 

  • Julapalli MR, Scher RK, Sybert VP, Siegfried EC, Bree AF (2009) Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome. Am J Med Genet A 149A:1900–1906

    PubMed  Google Scholar 

  • Kerr JB, Hutt KJ, Michalak EM, Cook M, Vandenberg CJ, Liew SH, Bouillet P, Mills A, Scott CL, Findlay JK et al (2012) DNA damage-induced primordial follicle oocyte apoptosis and loss of fertility require TAp63-mediated induction of Puma and Noxa. Mol Cell 48:343–352

    PubMed Central  CAS  PubMed  Google Scholar 

  • Kimura TE, Merritt AJ, Garrod DR (2007) Calcium-independent desmosomes of keratinocytes are hyper-adhesive. J Invest Dermatol 127:775–781

    CAS  PubMed  Google Scholar 

  • Kjaer KW, Hansen L, Schwabe GC, Marques-de-Faria AP, Eiberg H, Mundlos S, Tommerup N, Rosenberg T (2005) Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome). J Med Genet 42:292–298

    PubMed Central  CAS  PubMed  Google Scholar 

  • Koch PJ, Mahoney MG, Ishikawa H, Pulkkinen L, Uitto J, Shultz L, Murphy GF, Whitaker-Menezes D, Stanley JR (1997) Targeted disruption of the pemphigus vulgaris antigen (desmoglein 3) gene in mice causes loss of keratinocyte cell adhesion with a phenotype similar to pemphigus vulgaris. J Cell Biol 137:1091–1102

    PubMed Central  CAS  PubMed  Google Scholar 

  • Koch PJ, Dinella J, Fete M, Siegfried EC, Koster MI (2014) Modeling AEC-New approaches to study rare genetic disorders. Am J Med Genet A 164A:2443–2454

    PubMed  Google Scholar 

  • Koster MI, Dai D, Marinari B, Sano Y, Costanzo A, Karin M, Roop DR (2007) p63 induces key target genes required for epidermal morphogenesis. Proc Natl Acad Sci U S A 104:3255–3260

    PubMed Central  CAS  PubMed  Google Scholar 

  • Koster MI, Marinari B, Payne AS, Kantaputra PN, Costanzo A, Roop DR (2009) DeltaNp63 knockdown mice: a mouse model for AEC syndrome. Am J Med Genet A 149A:1942–1947

    PubMed Central  CAS  PubMed  Google Scholar 

  • Koster MI, Dinella J, Chen J, O’Shea C, Koch PJ (2014) Integrating animal models and in vitro tissue models to elucidate the role of desmosomal proteins in diseases. Cell Commun Adhes 21:55–63

    PubMed Central  CAS  PubMed  Google Scholar 

  • Kouwenhoven EN, van Heeringen SJ, Tena JJ, Oti M, Dutilh BE, Alonso ME, de la Calle-Mustienes E, Smeenk L, Rinne T, Parsaulian L et al (2010) Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus. PLoS Genet 6:e1001065

    PubMed Central  PubMed  Google Scholar 

  • Kroger C, Loschke F, Schwarz N, Windoffer R, Leube RE, Magin TM (2013) Keratins control intercellular adhesion involving PKC-alpha-mediated desmoplakin phosphorylation. J Cell Biol 201:681–692

    PubMed Central  CAS  PubMed  Google Scholar 

  • Kubo A, Nagao K, Yokouchi M, Sasaki H, Amagai M (2009) External antigen uptake by Langerhans cells with reorganization of epidermal tight junction barriers. J Exp Med 206:2937–2946

    PubMed Central  CAS  PubMed  Google Scholar 

  • Kurata S, Okuyama T, Osada M, Watanabe T, Tomimori Y, Sato S, Iwai A, Tsuji T, Ikawa Y, Katoh I (2004) p51/p63 Controls subunit alpha3 of the major epidermis integrin anchoring the stem cells to the niche. J Biol Chem 279:50069–50077

    CAS  PubMed  Google Scholar 

  • Lacouture ME (2006) Mechanisms of cutaneous toxicities to EGFR inhibitors. Nat Rev Cancer 6:803–812

    CAS  PubMed  Google Scholar 

  • Lane EB, Rugg EL, Navsaria H, Leigh IM, Heagerty AH, Ishida-Yamamoto A, Eady RA (1992) A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering. Nature 356:244–246

    CAS  PubMed  Google Scholar 

  • Langbein L, Grund C, Kuhn C, Praetzel S, Kartenbeck J, Brandner JM, Moll I, Franke WW (2002) Tight junctions and compositionally related junctional structures in mammalian stratified epithelia and cell cultures derived therefrom. Eur J Cell Biol 81:419–435

    CAS  PubMed  Google Scholar 

  • Laurikkala J, Mikkola ML, James M, Tummers M, Mills AA, Thesleff I (2006) p63 regulates multiple signalling pathways required for ectodermal organogenesis and differentiation. Development 133:1553–1563

    CAS  PubMed  Google Scholar 

  • Lee B, Villarreal-Ponce A, Fallahi M, Ovadia J, Sun P, Yu QC, Ito S, Sinha S, Nie Q, Dai X (2014) Transcriptional mechanisms link epithelial plasticity to adhesion and differentiation of epidermal progenitor cells. Dev Cell 29:47–58

    PubMed Central  PubMed  Google Scholar 

  • Lin S, Gordon K, Kaplan N, Getsios S (2010) Ligand targeting of EphA2 enhances keratinocyte adhesion and differentiation via desmoglein 1. Mol Biol Cell 21:3902–3914

    PubMed Central  CAS  PubMed  Google Scholar 

  • Litjens SH, de Pereda JM, Sonnenberg A (2006) Current insights into the formation and breakdown of hemidesmosomes. Trends Cell Biol 16:376–383

    CAS  PubMed  Google Scholar 

  • Livshits G, Kobielak A, Fuchs E (2012) Governing epidermal homeostasis by coupling cell-cell adhesion to integrin and growth factor signaling, proliferation, and apoptosis. Proc Natl Acad Sci U S A 109:4886–4891

    PubMed Central  CAS  PubMed  Google Scholar 

  • Lopardo T, Lo Iacono N, Marinari B, Giustizieri ML, Cyr DG, Merlo G, Crosti F, Costanzo A, Guerrini L (2008) Claudin-1 is a p63 target gene with a crucial role in epithelial development. PLoS ONE 3:e2715

    PubMed Central  PubMed  Google Scholar 

  • Lorch JH, Klessner J, Park JK, Getsios S, Wu YL, Stack MS, Green KJ (2004) Epidermal growth factor receptor inhibition promotes desmosome assembly and strengthens intercellular adhesion in squamous cell carcinoma cells. J Biol Chem 279:37191–37200

    CAS  PubMed  Google Scholar 

  • Marques MR, Ihrie RA, Horner JS, Attardi LD (2006) The requirement for perp in postnatal viability and epithelial integrity reflects an intrinsic role in stratified epithelia. J Invest Dermatol 126:69–73

    PubMed Central  CAS  PubMed  Google Scholar 

  • Matsushima H, Utani A, Endo H, Matsuura H, Kakuta M, Nakamura Y, Matsuyoshi N, Matsui C, Nakanishi H, Takai Y et al (2003) The expression of nectin-1alpha in normal human skin and various skin tumours. Br J Dermatol 148:755–762

    CAS  PubMed  Google Scholar 

  • McDade SS, Henry AE, Pivato GP, Kozarewa I, Mitsopoulos C, Fenwick K, Assiotis I, Hakas J, Zvelebil M, Orr N et al (2012) Genome-wide analysis of p63 binding sites identifies AP-2 factors as co-regulators of epidermal differentiation. Nucleic Acids Res 40:7190–7206

    PubMed Central  CAS  PubMed  Google Scholar 

  • McGrath JA, Gatalica B, Christiano AM, Li K, Owaribe K, McMillan JR, Eady RA, Uitto J (1995) Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa. Nat Genet 11:83–86

    CAS  PubMed  Google Scholar 

  • McGrath JA, Gatalica B, Li K, Dunnill MG, McMillan JR, Christiano AM, Eady RA, Uitto J (1996) Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition. Am J Pathol 148:1787–1796

    PubMed Central  CAS  PubMed  Google Scholar 

  • McGrath JA, McMillan JR, Shemanko CS, Runswick SK, Leigh IM, Lane EB, Garrod DR, Eady RA (1997) Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome. Nat Genet 17:240–244

    CAS  PubMed  Google Scholar 

  • McGrath JA, Duijf PH, Doetsch V, Irvine AD, de Waal R, Vanmolkot KR, Wessagowit V, Kelly A, Atherton DJ, Griffiths WA et al (2001) Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63. Hum Mol Genet 10:221–229

    CAS  PubMed  Google Scholar 

  • McGregor L, Makela V, Darling SM, Vrontou S, Chalepakis G, Roberts C, Smart N, Rutland P, Prescott N, Hopkins J et al (2003) Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. Nat Genet 34:203–208

    CAS  PubMed  Google Scholar 

  • McKoy G, Protonotarios N, Crosby A, Tsatsopoulou A, Anastasakis A, Coonar A, Norman M, Baboonian C, Jeffery S, McKenna WJ (2000) Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). Lancet 355:2119–2124

    CAS  PubMed  Google Scholar 

  • McLean WH, Pulkkinen L, Smith FJ, Rugg EL, Lane EB, Bullrich F, Burgeson RE, Amano S, Hudson DL, Owaribe K et al (1996) Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. Genes Dev 10:1724–1735

    CAS  PubMed  Google Scholar 

  • Michels C, Buchta T, Bloch W, Krieg T, Niessen CM (2009) Classical cadherins regulate desmosome formation. J Invest Dermatol 129:2072–2075

    CAS  PubMed  Google Scholar 

  • Mills AA, Zheng B, Wang XJ, Vogel H, Roop DR, Bradley A (1999) p63 is a p53 homologue required for limb and epidermal morphogenesis. Nature 398:708–713

    CAS  PubMed  Google Scholar 

  • Mills AA, Qi Y, Bradley A (2002) Conditional inactivation of p63 by Cre-mediated excision. Genesis 32:138–141

    CAS  PubMed  Google Scholar 

  • Mollo MR, Antonini D, Mitchell K, Fortugno P, Costanzo A, Dixon J, Brancati F and Missero C (2014) p63-dependent and independent mechanisms of nectin-1 and −4 regulation in the epidermis. Exp Dermatol (in press)

  • Moretti F, Marinari B, Lo Iacono N, Botti E, Giunta A, Spallone G, Garaffo G, Vernersson-Lindahl E, Merlo G, Mills AA et al (2010) A regulatory feedback loop involving p63 and IRF6 links the pathogenesis of 2 genetically different human ectodermal dysplasias. J Clin Invest 120:1570–1577

    PubMed Central  CAS  PubMed  Google Scholar 

  • Morita K, Itoh M, Saitou M, Ando-Akatsuka Y, Furuse M, Yoneda K, Imamura S, Fujimoto K, Tsukita S (1998) Subcellular distribution of tight junction-associated proteins (occludin, ZO-1, ZO-2) in rodent skin. J Invest Dermatol 110:862–866

    CAS  PubMed  Google Scholar 

  • Nguyen BC, Lefort K, Mandinova A, Antonini D, Devgan V, Della Gatta G, Koster MI, Zhang Z, Wang J, Tommasi di Vignano A et al (2006) Cross-regulation between Notch and p63 in keratinocyte commitment to differentiation. Genes Dev 20:1028–1042

    PubMed Central  CAS  PubMed  Google Scholar 

  • Norgett EE, Hatsell SJ, Carvajal-Huerta L, Cabezas JC, Common J, Purkis PE, Whittock N, Leigh IM, Stevens HP, Kelsell DP (2000) Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum Mol Genet 9:2761–2766

    CAS  PubMed  Google Scholar 

  • Osada M, Nagakawa Y, Park HL, Yamashita K, Wu G, Kim MS, Fomenkov A, Trink B, Sidransky D (2005) p63-specific activation of the BPAG-1e promoter. J Invest Dermatol 125:52–60

    CAS  PubMed  Google Scholar 

  • Payne AS, Yan AC, Ilyas E, Li W, Seykora JT, Young TL, Pawel BR, Honig PJ, Camacho J, Imaizumi S et al (2005) Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype. Arch Dermatol 141:1567–1573

    PubMed  Google Scholar 

  • Pellegrini G, Dellambra E, Golisano O, Martinelli E, Fantozzi I, Bondanza S, Ponzin D, McKeon F, De Luca M (2001) p63 identifies keratinocyte stem cells. Proc Natl Acad Sci U S A 98:3156–3161

    PubMed Central  CAS  PubMed  Google Scholar 

  • Petiot A, Conti FJ, Grose R, Revest JM, Hodivala-Dilke KM, Dickson C (2003) A crucial role for Fgfr2-IIIb signalling in epidermal development and hair follicle patterning. Development 130:5493–5501

    CAS  PubMed  Google Scholar 

  • Petrof G, Mellerio JE, McGrath JA (2012) Desmosomal genodermatoses. Br J Dermatol 166:36–45

    CAS  PubMed  Google Scholar 

  • Pigors M, Kiritsi D, Krumpelmann S, Wagner N, He Y, Podda M, Kohlhase J, Hausser I, Bruckner-Tuderman L, Has C (2011) Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity. Hum Mol Genet 20:1811–1819

    CAS  PubMed  Google Scholar 

  • Pulkkinen L, Kimonis VE, Xu Y, Spanou EN, McLean WH, Uitto J (1997) Homozygous alpha6 integrin mutation in junctional epidermolysis bullosa with congenital duodenal atresia. Hum Mol Genet 6:669–674

    CAS  PubMed  Google Scholar 

  • Pummi K, Malminen M, Aho H, Karvonen SL, Peltonen J, Peltonen S (2001) Epidermal tight junctions: ZO-1 and occludin are expressed in mature, developing, and affected skin and in vitro differentiating keratinocytes. J Invest Dermatol 117:1050–1058

    CAS  PubMed  Google Scholar 

  • Qiao F, Bowie JU (2005) The many faces of SAM. Sci STKE 2005:re7

  • Raghavan S, Bauer C, Mundschau G, Li Q, Fuchs E (2000) Conditional ablation of beta1 integrin in skin. Severe defects in epidermal proliferation, basement membrane formation, and hair follicle invagination. J Cell Biol 150:1149–1160

    PubMed Central  CAS  PubMed  Google Scholar 

  • Rama P, Matuska S, Paganoni G, Spinelli A, De Luca M, Pellegrini G (2010) Limbal stem-cell therapy and long-term corneal regeneration. N Engl J Med 363:147–155

    CAS  PubMed  Google Scholar 

  • Rickman L, Simrak D, Stevens HP, Hunt DM, King IA, Bryant SP, Eady RA, Leigh IM, Arnemann J, Magee AI et al (1999) N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma. Hum Mol Genet 8:971–976

    CAS  PubMed  Google Scholar 

  • Rikitake Y, Mandai K, Takai Y (2012) The role of nectins in different types of cell-cell adhesion. J Cell Sci 125:3713–3722

    CAS  PubMed  Google Scholar 

  • Rinne T, Brunner HG, van Bokhoven H (2007) p63-associated disorders. Cell Cycle 6:262–268

    CAS  PubMed  Google Scholar 

  • Rinne T, Clements SE, Lamme E, Duijf PH, Bolat E, Meijer R, Scheffer H, Rosser E, Tan TY, McGrath JA et al (2008) A novel translation re-initiation mechanism for the p63 gene revealed by amino-terminal truncating mutations in Rapp-Hodgkin/Hay-Wells-like syndromes. Hum Mol Genet 17:1968–1977

    CAS  PubMed  Google Scholar 

  • Rinne T, Bolat E, Meijer R, Scheffer H, van Bokhoven H (2009) Spectrum of p63 mutations in a selected patient cohort affected with ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (AEC). Am J Med Genet A 149A:1948–1951

    CAS  PubMed  Google Scholar 

  • Rizzo JM, Romano RA, Bard J, Sinha S (2014) RNA-seq studies reveal new insights into p63 and the transcriptomic landscape of the mouse skin. J Invest Dermatol (in press)

  • Romano RA, Smalley K, Liu S, Sinha S (2010) Abnormal hair follicle development and altered cell fate of follicular keratinocytes in transgenic mice expressing DeltaNp63alpha. Development 137:1431–1439

    PubMed Central  CAS  PubMed  Google Scholar 

  • Romano RA, Smalley K, Magraw C, Serna VA, Kurita T, Raghavan S, Sinha S (2012) DeltaNp63 knockout mice reveal its indispensable role as a master regulator of epithelial development and differentiation. Development 139:772–782

    PubMed Central  CAS  PubMed  Google Scholar 

  • Rouleau M, Puceat M, Aberdam D (2011) Unexpected role for p63 during heart development: one phenotype can hide another one. Med Sci 27:905–909

    Google Scholar 

  • Ruhrberg C, Hajibagheri MA, Simon M, Dooley TP, Watt FM (1996) Envoplakin, a novel precursor of the cornified envelope that has homology to desmoplakin. J Cell Biol 134:715–729

    CAS  PubMed  Google Scholar 

  • Ruhrberg C, Hajibagheri MA, Parry DA, Watt FM (1997) Periplakin, a novel component of cornified envelopes and desmosomes that belongs to the plakin family and forms complexes with envoplakin. J Cell Biol 139:1835–1849

    PubMed Central  CAS  PubMed  Google Scholar 

  • Ruzzi L, Gagnoux-Palacios L, Pinola M, Belli S, Meneguzzi G, D’Alessio M, Zambruno G (1997) A homozygous mutation in the integrin alpha6 gene in junctional epidermolysis bullosa with pyloric atresia. J Clin Invest 99:2826–2831

    PubMed Central  CAS  PubMed  Google Scholar 

  • Ryynanen M, Ryynanen J, Sollberg S, Iozzo RV, Knowlton RG, Uitto J (1992) Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils. J Clin Invest 89:974–980

    PubMed Central  CAS  PubMed  Google Scholar 

  • Samuelov L, Sarig O, Harmon RM, Rapaport D, Ishida-Yamamoto A, Isakov O, Koetsier JL, Gat A, Goldberg I, Bergman R et al (2013) Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting. Nat Genet 45:1244–1248

    PubMed Central  CAS  PubMed  Google Scholar 

  • Schluter H, Wepf R, Moll I, Franke WW (2004) Sealing the live part of the skin: the integrated meshwork of desmosomes, tight junctions and curvilinear ridge structures in the cells of the uppermost granular layer of the human epidermis. Eur J Cell Biol 83:655–665

    PubMed  Google Scholar 

  • Senoo M, Pinto F, Crum CP, McKeon F (2007) p63 Is essential for the proliferative potential of stem cells in stratified epithelia. Cell 129:523–536

    CAS  PubMed  Google Scholar 

  • Shalom-Feuerstein R, Lena AM, Zhou H, De La Forest Divonne S, Van Bokhoven H, Candi E, Melino G, Aberdam D (2011) DeltaNp63 is an ectodermal gatekeeper of epidermal morphogenesis. Cell Death Differ 18:887–896

    PubMed Central  CAS  PubMed  Google Scholar 

  • Shen J, van den Bogaard EH, Kouwenhoven EN, Bykov VJ, Rinne T, Zhang Q, Tjabringa GS, Gilissen C, van Heeringen SJ, Schalkwijk J et al (2013) APR-246/PRIMA-1(MET) rescues epidermal differentiation in skin keratinocytes derived from EEC syndrome patients with p63 mutations. Proc Natl Acad Sci U S A 110:2157–2162

    PubMed Central  CAS  PubMed  Google Scholar 

  • Shimomura Y, Wajid M, Shapiro L, Christiano AM (2008) P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle. Development 135:743–753

    CAS  PubMed  Google Scholar 

  • Simpson CL, Patel DM, Green KJ (2011) Deconstructing the skin: cytoarchitectural determinants of epidermal morphogenesis. Nat Rev Mol Cell Biol 12:565–580

    PubMed Central  CAS  PubMed  Google Scholar 

  • Smith FJ, Eady RA, Leigh IM, McMillan JR, Rugg EL, Kelsell DP, Bryant SP, Spurr NK, Geddes JF, Kirtschig G et al (1996) Plectin deficiency results in muscular dystrophy with epidermolysis bullosa. Nat Genet 13:450–457

    CAS  PubMed  Google Scholar 

  • Sozen MA, Suzuki K, Tolarova MM, Bustos T, Fernandez Iglesias JE, Spritz RA (2001) Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela. Nat Genet 29:141–142

    CAS  PubMed  Google Scholar 

  • Sprecher E, Bergman R, Richard G, Lurie R, Shalev S, Petronius D, Shalata A, Anbinder Y, Leibu R, Perlman I et al (2001) Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin. Nat Genet 29:134–136

    CAS  PubMed  Google Scholar 

  • Straub WE, Weber TA, Schafer B, Candi E, Durst F, Ou HD, Rajalingam K, Melino G, Dotsch V (2010) The C-terminus of p63 contains multiple regulatory elements with different functions. Cell Death Dis 1:e5

    PubMed Central  CAS  PubMed  Google Scholar 

  • Su X, Paris M, Gi YJ, Tsai KY, Cho MS, Lin YL, Biernaskie JA, Sinha S, Prives C, Pevny LH et al (2009) TAp63 prevents premature aging by promoting adult stem cell maintenance. Cell Stem Cell 5:64–75

    PubMed Central  CAS  PubMed  Google Scholar 

  • Su X, Chakravarti D, Cho MS, Liu L, Gi YJ, Lin YL, Leung ML, El-Naggar A, Creighton CJ, Suraokar MB et al (2010) TAp63 suppresses metastasis through coordinate regulation of Dicer and miRNAs. Nature 467:986–990

    PubMed Central  CAS  PubMed  Google Scholar 

  • Suh EK, Yang A, Kettenbach A, Bamberger C, Michaelis AH, Zhu Z, Elvin JA, Bronson RT, Crum CP, McKeon F (2006) p63 protects the female germ line during meiotic arrest. Nature 444:624–628

    CAS  PubMed  Google Scholar 

  • Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA (2000) Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nat Genet 25:427–430

    CAS  PubMed  Google Scholar 

  • Tachibana K, Nakanishi H, Mandai K, Ozaki K, Ikeda W, Yamamoto Y, Nagafuchi A, Tsukita S, Takai Y (2000) Two cell adhesion molecules, nectin and cadherin, interact through their cytoplasmic domain-associated proteins. J Cell Biol 150:1161–1176

    PubMed Central  CAS  PubMed  Google Scholar 

  • Tani H, Morris RJ, Kaur P (2000) Enrichment for murine keratinocyte stem cells based on cell surface phenotype. Proc Natl Acad Sci U S A 97:10960–10965

    PubMed Central  CAS  PubMed  Google Scholar 

  • Thomason HA, Zhou H, Kouwenhoven EN, Dotto GP, Restivo G, Nguyen BC, Little H, Dixon MJ, van Bokhoven H, Dixon J (2010) Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice. J Clin Invest 120:1561–1569

    PubMed Central  CAS  PubMed  Google Scholar 

  • Tinkle CL, Lechler T, Pasolli HA, Fuchs E (2004) Conditional targeting of E-cadherin in skin: insights into hyperproliferative and degenerative responses. Proc Natl Acad Sci U S A 101:552–557

    PubMed Central  CAS  PubMed  Google Scholar 

  • Tinkle CL, Pasolli HA, Stokes N, Fuchs E (2008) New insights into cadherin function in epidermal sheet formation and maintenance of tissue integrity. Proc Natl Acad Sci U S A 105:15405–15410

    PubMed Central  CAS  PubMed  Google Scholar 

  • Truong AB, Kretz M, Ridky TW, Kimmel R, Khavari PA (2006) p63 regulates proliferation and differentiation of developmentally mature keratinocytes. Genes Dev 20:3185–3197

    PubMed Central  CAS  PubMed  Google Scholar 

  • Tsukita S, Furuse M (2002) Claudin-based barrier in simple and stratified cellular sheets. Curr Opin Cell Biol 14:531–536

    CAS  PubMed  Google Scholar 

  • Tumbar T, Guasch G, Greco V, Blanpain C, Lowry WE, Rendl M, Fuchs E (2004) Defining the epithelial stem cell niche in skin. Science 303:359–363

    PubMed Central  CAS  PubMed  Google Scholar 

  • Turksen K, Troy TC (2002) Permeability barrier dysfunction in transgenic mice overexpressing claudin 6. Development 129:1775–1784

    CAS  PubMed  Google Scholar 

  • Uitto J, Christiano AM, McLean WH, McGrath JA (2012) Novel molecular therapies for heritable skin disorders. J Invest Dermatol 132:820–828

    PubMed Central  CAS  PubMed  Google Scholar 

  • van der Neut R, Krimpenfort P, Calafat J, Niessen CM, Sonnenberg A (1996) Epithelial detachment due to absence of hemidesmosomes in integrin beta 4 null mice. Nat Genet 13:366–369

    PubMed  Google Scholar 

  • Van Itallie CM, Anderson JM (2014) Architecture of tight junctions and principles of molecular composition. Semin Cell Dev Biol (in press)

  • Vanbokhoven H, Melino G, Candi E, Declercq W (2011) p63, a story of mice and men. J Invest Dermatol 131:1196–1207

    CAS  PubMed  Google Scholar 

  • Vasioukhin V, Bauer C, Degenstein L, Wise B, Fuchs E (2001a) Hyperproliferation and defects in epithelial polarity upon conditional ablation of alpha-catenin in skin. Cell 104:605–617

    CAS  PubMed  Google Scholar 

  • Vasioukhin V, Bowers E, Bauer C, Degenstein L, Fuchs E (2001b) Desmoplakin is essential in epidermal sheet formation. Nat Cell Biol 3:1076–1085

    CAS  PubMed  Google Scholar 

  • Vernersson Lindahl E, Garcia EL, Mills AA (2013) An allelic series of Trp63 mutations defines TAp63 as a modifier of EEC syndrome. Am J Med Genet A 161A:1961–1971

    PubMed  Google Scholar 

  • Vidal F, Aberdam D, Miquel C, Christiano AM, Pulkkinen L, Uitto J, Ortonne JP, Meneguzzi G (1995) Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia. Nat Genet 10:229–234

    CAS  PubMed  Google Scholar 

  • Vigano MA, Lamartine J, Testoni B, Merico D, Alotto D, Castagnoli C, Robert A, Candi E, Melino G, Gidrol X et al (2006) New p63 targets in keratinocytes identified by a genome-wide approach. EMBO J 25:5105–5116

    PubMed Central  CAS  PubMed  Google Scholar 

  • Yang A, Kaghad M, Wang Y, Gillett E, Fleming MD, Dotsch V, Andrews NC, Caput D, McKeon F (1998) p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities. Mol Cell 2:305–316

    CAS  PubMed  Google Scholar 

  • Yang A, Schweitzer R, Sun D, Kaghad M, Walker N, Bronson RT, Tabin C, Sharpe A, Caput D, Crum C et al (1999) p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature 398:714–718

    CAS  PubMed  Google Scholar 

  • Yang A, Zhu Z, Kapranov P, McKeon F, Church GM, Gingeras TR, Struhl K (2006) Relationships between p63 binding, DNA sequence, transcription activity, and biological function in human cells. Mol Cell 24:593–602

    CAS  PubMed  Google Scholar 

  • Yang XH, Mirchev R, Deng X, Yacono P, Yang HL, Golan DE, Hemler ME (2012) CD151 restricts the alpha6 integrin diffusion mode. J Cell Sci 125:1478–1487

    PubMed Central  CAS  PubMed  Google Scholar 

  • Yokoyama S, Tachibana K, Nakanishi H, Yamamoto Y, Irie K, Mandai K, Nagafuchi A, Monden M, Takai Y (2001) alpha-catenin-independent recruitment of ZO-1 to nectin-based cell-cell adhesion sites through afadin. Mol Biol Cell 12:1595–1609

    PubMed Central  CAS  PubMed  Google Scholar 

  • Young P, Boussadia O, Halfter H, Grose R, Berger P, Leone DP, Robenek H, Charnay P, Kemler R, Suter U (2003) E-cadherin controls adherens junctions in the epidermis and the renewal of hair follicles. EMBO J 22:5723–5733

    PubMed Central  CAS  PubMed  Google Scholar 

  • Yu Z, Lin KK, Bhandari A, Spencer JA, Xu X, Wang N, Lu Z, Gill GN, Roop DR, Wertz P et al (2006) The Grainyhead-like epithelial transactivator Get-1/Grhl3 regulates epidermal terminal differentiation and interacts functionally with LMO4. Dev Biol 299:122–136

    CAS  PubMed  Google Scholar 

  • Yu Z, Mannik J, Soto A, Lin KK, Andersen B (2009) The epidermal differentiation-associated Grainyhead gene Get1/Grhl3 also regulates urothelial differentiation. EMBO J 28:1890–1903

    PubMed Central  CAS  PubMed  Google Scholar 

  • Yurchenco PD (2011) Basement membranes: cell scaffoldings and signaling platforms. Cold Spring Harb Perspect Biol 3

  • Zarnegar BJ, Webster DE, Lopez-Pajares V, Vander Stoep Hunt B, Qu K, Yan KJ, Berk DR, Sen GL, Khavari PA (2012) Genomic profiling of a human organotypic model of AEC syndrome reveals ZNF750 as an essential downstream target of mutant TP63. Am J Hum Genet 91:435–443

    PubMed Central  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Dario Antonini for critical reading of the manuscript and for generating the schematic figures. Work in the laboratory of Caterina Missero is supported by Telethon, Italy (GGP09230), the European ERA-Net Research Program on Rare Diseases (E-Rare-2; Skindev) and the Italian Association for Cancer Research (AIRC; IG11369). The authors have no financial interests to disclose.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Caterina Missero.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ferone, G., Mollo, M.R. & Missero, C. Epidermal cell junctions and their regulation by p63 in health and disease. Cell Tissue Res 360, 513–528 (2015). https://doi.org/10.1007/s00441-014-2108-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00441-014-2108-1

Keywords