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Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia

Abstract

Cleft lip, with or without cleft palate (CL/P), is one of the most common birth defects, occurring in 0.4 to 2.0 per 1,000 infants born alive1. Approximately 70% of CL/P cases are non-syndromic (MIM 119530), but CL/P also occurs in many single-gene syndromes, each affecting a protein critical for orofacial development. Here we describe positional cloning of the gene responsible for an autosomal recessive CL/P-ectodermal dysplasia (ED) syndrome (CLPED1; previously ED4; ref. 2), which we identify as PVRL1, encoding nectin-1, an immunoglobulin (Ig)-related transmembrane cell-cell adhesion molecule that is part of the NAP cell adhesion system3,4,5,6. Nectin-1 is also the principal cell surface receptor for α-herpesviruses (HveC; ref. 7), and the high frequency of CLPED1 on Margarita Island in the Caribbean Sea might result from resistance of heterozygotes to infection by these viruses.

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Figure 1: Positional cloning of the CLPED1 locus.
Figure 2: PVRL1 mutations in CLPED1 patients.
Figure 3: Expression of Pvrl1 mRNA during mouse embryo development.

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References

  1. Schutte, B.C. & Murray, J.C. The many faces and factors of orofacial clefts. Hum. Mol. Genet. 8, 1853–1859 (1999).

    Article  CAS  Google Scholar 

  2. Suzuki, K., Bustos, T. & Spritz, R.A. Linkage disequilibrium mapping of the gene for Margarita Island ectodermal dysplasia (ED4) to 11q23. Am. J. Hum. Genet. 63,1102–1107 (1998).

    Article  CAS  Google Scholar 

  3. Takahashi, K. et al. Nectin/PRR: an immunoglobulin-like cell adhesion molecule recruited to cadherin-based adherens junctions through interaction with Afadin, a PDZ domain-containing protein. J. Cell Biol. 139, 517–549 (1999).

    Google Scholar 

  4. Mandai, K. et al. Afadin: a novel actin filament-binding protein with one PDZ domain localized at cadherin-based cell-to-cell adherens junction. J. Cell Biol. 139, 517–528 (1997).

    Article  CAS  Google Scholar 

  5. Mandai, K. et al. Ponsin/SH3P12: an l-afadin- and vinculin-binding protein localized at cell-cell and cell-matrix adherens junctions. J. Cell Biol. 144, 1001–1017 (1999).

    Article  CAS  Google Scholar 

  6. Asakura, T. et al. Similar and differential behaviour between the nectin-afadin-ponsin and cadherin-catenin systems during the formation and disruption of the polarized junctional alignment in epithelial cells. Genes Cells 4, 573–581 (1999).

    Article  CAS  Google Scholar 

  7. Geraghty, R.J., Krummenacher, C., Cohen, G.H., Eisenberg, R.J. & Spear, P.G. Entry of alphaherpesviruses mediated by poliovirus receptor-related protein 1 and poliovirus receptor. Science 280,1618–1620 (1998).

    Article  CAS  Google Scholar 

  8. Zlotogora, J., Zilberman, Y., Tenenbaum, A. & Wexler, M.R. Cleft lip and palate, pili torti, malformed ears, partial syndactyly of fingers and toes and mental retardation. A new syndrome? J. Med. Genet. 24, 291–293 (1987).

    Article  CAS  Google Scholar 

  9. Ogur, G. & Yüksel, M. Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey. J. Med. Genet. 25, 37–40 (1988).

    Article  CAS  Google Scholar 

  10. Zlotogora, J. & Ogur, G. Syndactyly, ectodermal dysplasia, and cleft lip and palate. J. Med. Genet. 25, 503 (1988).

    Article  CAS  Google Scholar 

  11. Rodini, E.S.O. & Richieri-Costa, A. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome. Am. J. Med. Genet. 36, 473–476 (1990).

    Article  CAS  Google Scholar 

  12. Zlotogora, J. Syndactyly, ectodermal dysplasia, and cleft lip/palate. J. Med. Genet. 31, 957–959 (1994).

    Article  CAS  Google Scholar 

  13. Bustos, T. et al. Autosomal recessive ectodermal dysplasia: I. An undescribed dysplasia/malformation syndrome. Am. J. Med. Genet. 41, 398–404 (1991).

    Article  CAS  Google Scholar 

  14. Buckler, A.J. et al. Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. Proc. Natl Acad. Sci. USA 88, 4005–4009 (1991).

    Article  CAS  Google Scholar 

  15. Altschul, S.F. et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25, 3389–3402 (1997).

    Article  CAS  Google Scholar 

  16. Leonhardt, E.A., Kapp, L.N., Young, B.R. & Murnane, J.P. Nucleotide sequence analysis of a candidate gene for ataxia-telangiectasia group D (ATDC). Genomics 19, 130–136 (1994).

    Article  CAS  Google Scholar 

  17. Lee, S.-T., Park, S.-K., Lee, K.-H., Holmes, S.A. & Spritz, R.A. A non-radioactive method for simultaneous detection of single-strand conformation polymorphisms (SSCPs) and heteroduplexes. Molecules Cells 5, 668–672 (1995).

    CAS  Google Scholar 

  18. Lopez, M. et al. Complementary DNA characterization and chromosomal localization of a human gene related to the poliovirus receptor-encoding gene. Gene 155, 261–265 (1995).

    Article  CAS  Google Scholar 

  19. Cocchi, F. et al. The V domain of herpesvirus Ig-like receptor (HIgR) contains a major functional region in herpes simplex virus-1 entry into cells and interacts physically with the viral glycoprotein D. Proc. Natl Acad. Sci. USA 95, 15700–15705 (1998).

    Article  CAS  Google Scholar 

  20. Celli, J. et al. Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome. Cell 99, 143–153 (1999).

    Article  CAS  Google Scholar 

  21. van den Boogaard, M.-J.H., Dorland, M., Beemer, F.A. & van Amstel, H.K.P. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans. Nature Genet. 24, 342–343 (2000).

    Article  CAS  Google Scholar 

  22. Mendelsohn, C.L., Wimmer, E. & Racaniello, V.R. Cellular receptor for poliovirus: molecular cloning, nucleotide sequence, and expression of a new member of the immunoglobulin superfamily. Cell 56, 855–865 (1989).

    Article  CAS  Google Scholar 

  23. Koike, S. et al. The poliovirus receptor protein is produced both as membrane-bound and secreted forms. EMBO J. 9, 3217–3224 (1990).

    Article  CAS  Google Scholar 

  24. Eberle, F., Dubreuil, P., Mattei, M.G., Devilard, E. & Lopez, M. The human PRR2 gene, related to the human poliovirus receptor gene (PVR), is the true homolog of the murine MPH gene. Gene 159, 267–272 (1995).

    Article  CAS  Google Scholar 

  25. Schonk, D. et al. Assignment of seven genes to distinct intervals on the midportion of human chromosome 19q surrounding the myotonic dystrophy gene region. Cytogenet. Cell Genet. 54, 15–19 (1990).

    Article  CAS  Google Scholar 

  26. Trask, B. et al. Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers. Genomics 15, 133–145 (1993).

    Article  CAS  Google Scholar 

  27. Stein, J. et al. Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families. Am. J. Hum. Genet. 57, 257–272 (1995).

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Amos, C., Gasser, D. & Hecht, J.T. Nonsyndromic cleft lip with or without cleft palate: new BCL3 information. Am. J. Hum. Genet. 59, 743–744 (1996).

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Wyszynski, D.F. et al. Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families. Hum. Genet. 99, 22–26 (1997).

    Article  CAS  Google Scholar 

  30. Helms, J.A. et al. Sonic hedgehog participates in craniofacial morphogenesis and is down-regulated by teratogenic doses of retinoic acid. Dev. Biol. 186, 25–35 (1997).

    Article  Google Scholar 

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Acknowledgements

We thank C. Jones for PAC p32o11; and D. Shukla and P.G. Spear for the unpublished mouse Pvrl1 cDNA sequence. This work was supported by grants from the March of Dimes Birth Defects Foundation (FY99-609) and the National Foundation for Ectodermal Dysplasia to R.A.S. and the National Institutes of Health (HD01079, DE12462) to J.A.H.

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Correspondence to Richard A. Spritz.

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Suzuki, K., Hu, D., Bustos, T. et al. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nat Genet 25, 427–430 (2000). https://doi.org/10.1038/78119

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