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Functional comparison of the upstream regulatory DNA sequences of four human epidermal keratin genes.
Jiang, C K; Epstein, H S; Tomic, M; Freedberg, I M; Blumenberg, M.
Afiliação
  • Jiang CK; Departments of Dermatology, New York University Medical Center, NY 10016.
J Invest Dermatol ; 96(2): 162-7, 1991 Feb.
Article em En | MEDLINE | ID: mdl-1704037
The promoters of epidermal keratin genes, K5, K6, and K10 were cloned and their functions compared with that of the previously described promoter of the K14 keratin gene in non-epithelial and transformed epithelial cell lines, as well as in primary cultures of cells derived from simple and stratified epithelia. The four promoters were functional only in epithelial cells. Although the promoter for the basal cell-specific, acidic-type K14 gene was active in all epithelial cells tested, its basic-type partner, K5, and the promoter for the hyper-proliferation-associated K6 were active only in primary cultures of stratified epithelia. The promoter for the epidermal differentiation-specific K10 keratin gene was active at a low level in primary cultures of stratified epithelial cells on non-epidermal origin. Thus, the K14 gene promoter is functional in all epithelial cells, but the upstream regions of the K5 and K6 keratin genes restrict their expression to stratified epithelia, whereas the epidermal determinants of the K10 gene are not in the proximal upstream sequences.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequências Reguladoras de Ácido Nucleico / Regiões Promotoras Genéticas / Epiderme / Queratinas Limite: Humans Idioma: En Revista: J Invest Dermatol Ano de publicação: 1991 Tipo de documento: Article País de publicação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequências Reguladoras de Ácido Nucleico / Regiões Promotoras Genéticas / Epiderme / Queratinas Limite: Humans Idioma: En Revista: J Invest Dermatol Ano de publicação: 1991 Tipo de documento: Article País de publicação: Estados Unidos