Literature DB >> 8663392

Cloning of the gene for human pemphigus vulgaris antigen (desmoglein 3), a desmosomal cadherin. Characterization of the promoter region and identification of a keratinocyte-specific cis-element.

S A Silos1, K Tamai, K Li, S Kivirikko, D Kouba, A M Christiano, J Uitto.   

Abstract

Pemphigus vulgaris antigen is a cadherin-like desmosomal cell adhesion molecule expressed primarily in suprabasal keratinocytes within the epidermis. Previously characterized structural features have defined this molecule as a desmoglein, DSG3. In this study, we have cloned the human DSG3 gene and examined the transcriptional regulation of its expression. The total gene consisted of 15 exons and was estimated to span >23 kilobases. Comparison of exon-intron organization of DSG3 with bovine DSG1 and several classical cadherin genes revealed striking conservation of the structure. Up to 2.8 kilobases of the upstream genomic sequences were sequenced and found to contain several putative cis-regulatory elements. The promoter region was GC-rich and TATA-less, similar to previously characterized mammalian cadherin promoters. The putative promoter region was subcloned into a vector containing chloramphenicol acetyl transferase reporter gene. Transient transfections with a series of deletion clones indicated that the DSG3 promoter demonstrated keratinocyte-specific expression, as compared with dermal fibroblasts examined in parallel, and fine mapping identified a 30-base pair segment at -200 to -170 capable of conferring epidermal specific expression. The results provide evidence for the transcriptional regulation of the pemphigus vulgaris antigen gene, potentially critical for development of the epidermis and physiologic terminal differentiation of keratinocytes.

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Year:  1996        PMID: 8663392     DOI: 10.1074/jbc.271.29.17504

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  6 in total

1.  A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis.

Authors:  Muhammad Arshad Rafiq; Muhammad Ansar; Saqib Mahmood; Sayedul Haque; Muhammad Faiyaz-ul-Haque; Suzanne M Leal; Wasim Ahmad
Journal:  J Invest Dermatol       Date:  2004-07       Impact factor: 8.551

Review 2.  Desmosomes: regulators of cellular signaling and adhesion in epidermal health and disease.

Authors:  Jodi L Johnson; Nicole A Najor; Kathleen J Green
Journal:  Cold Spring Harb Perspect Med       Date:  2014-11-03       Impact factor: 6.915

3.  Characterization of the regulatory regions in the human desmoglein genes encoding the pemphigus foliaceous and pemphigus vulgaris antigens.

Authors:  M J Adams; M B Reichel; I A King; M D Marsden; M D Greenwood; H Thirlwell; J Arnemann; R S Buxton; R R Ali
Journal:  Biochem J       Date:  1998-01-01       Impact factor: 3.857

4.  Stat3 regulates desmoglein 3 transcription in epithelial keratinocytes.

Authors:  Xuming Mao; Michael Jeffrey T Cho; Christoph T Ellebrecht; Eric M Mukherjee; Aimee S Payne
Journal:  JCI Insight       Date:  2017-05-04

5.  A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.

Authors:  Muhammad Arshad Rafique; Muhammad Ansar; Syed Muhammad Jamal; Sajid Malik; Muhammad Sohail; Mohammad Faiyaz-Ul-Haque; Sayedul Haque; Suzanne M Leal; Wasim Ahmad
Journal:  Eur J Hum Genet       Date:  2003-08       Impact factor: 4.246

6.  Regulation of desmocollin gene expression in the epidermis: CCAAT/enhancer-binding proteins modulate early and late events in keratinocyte differentiation.

Authors:  Conrad Smith; Kuichun Zhu; Anita Merritt; Rhian Picton; Denise Youngs; David Garrod; Martyn Chidgey
Journal:  Biochem J       Date:  2004-06-15       Impact factor: 3.857

  6 in total

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