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      Autoantibodies against a novel epithelial cadherin in pemphigus vulgaris, a disease of cell adhesion

      , ,
      Cell
      Elsevier BV

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          Abstract

          Pemphigus vulgaris (PV) is a life-threatening skin disease in which autoantibodies against a keratinocyte cell surface 130 kd glycoprotein, PV antigen (PVA), cause loss of cell-cell adhesion, with resultant epidermal blisters. We used affinity-purified PV IgG to isolate cDNA, containing the entire coding sequence for PVA, from human keratinocyte expression libraries. Northern blot analysis indicated PV mRNA expression only in stratified squamous epithelia. The deduced amino acid sequence of PVA was unique but showed significant homology with members of the cadherin family of Ca(2+)-dependent cell adhesion molecules, most markedly to desmoglein I. These findings demonstrate that a novel epithelial cadherin is the target of autoantibodies in PV.

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          Most cited references37

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          A comprehensive set of sequence analysis programs for the VAX.

          The University of Wisconsin Genetics Computer Group (UWGCG) has been organized to develop computational tools for the analysis and publication of biological sequence data. A group of programs that will interact with each other has been developed for the Digital Equipment Corporation VAX computer using the VMS operating system. The programs available and the conditions for transfer are described.
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            Cadherins: a molecular family important in selective cell-cell adhesion.

            M Takeichi (1989)
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              A simple and very efficient method for generating cDNA libraries.

              A simple method for generating cDNA libraries from submicrogram quantities of mRNA is described. It combines classical first-strand synthesis with the novel RNase H-DNA polymerase I-mediated second-strand synthesis [Okayama, H., and Berg, P., Mol. Cell. Biol. 2 (1982) 161-170]. Neither the elaborate vector-primer system nor the classical hairpin loop cleavage by S1 nuclease are used. cDNA thus made can be tailed and cloned without further purification or sizing. Cloning efficiencies can be as high as 10(6) recombinants generated per microgram mRNA, a considerable improvement over earlier methods. Using the fully sequenced 1300 nucleotide-long bovine preproenkephalin mRNA, we have established by sequencing that the method yields faithful full-length transcripts. This procedure considerably simplifies the establishment of cDNA libraries and thus the cloning of low-abundance mRNAs.
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                Author and article information

                Journal
                Cell
                Cell
                Elsevier BV
                00928674
                November 1991
                November 1991
                : 67
                : 5
                : 869-877
                Article
                10.1016/0092-8674(91)90360-B
                1720352
                f6498a76-9905-42a0-b0e9-0ee6c920d1b7
                © 1991

                https://www.elsevier.com/tdm/userlicense/1.0/

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