We report the cloning and characterization of a murine epidermal differentiation gene, repetin (Rptn), exhibiting striking similarity to the genes of the intermediate filament-associated proteins profilaggrin and trichohyalin. The repetin gene consists of three exons and two introns. The first exon is short and untranslated. The deduced amino acid sequence distributed between exons II and III contains 1130 amino acids with a calculated molecular mass of 130 kDa and pI of 7.7. The amino terminus exhibits significant homology to the S100 proteins containing two calcium-binding motifs of the EF-hand type. The remainder coding sequence contains a central segment consisting of 49 tandem repeats of a 12-amino-acid sequence rich in glutamines. By fluorescence in situ hybridization the repetin gene was localized to chromosome band 3 F1-2. Expression of repetin mRNA is detectable in the stratified internal epithelia of forestomach and tongue and to a lesser degree in normal skin epidermis, where it is restricted to the differentiated suprabasal cell layers. Based on its chromosomal localization, its genomic organization, and its stage-specific expression during late epidermal differentiation, as well as on the structural features of the encoded protein, we conclude that the repetin gene represents a novel member of the ''fused gene'' subgroup of the S100 gene family encoding multifunctional epidermal matrix proteins. (C) 1997 Academic Press.
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Univ Bordeaux 2, INRA, UMR Genom Divers & Pouvoir Pathogene, IBVM, BP81, Villenave Dornon, FranceUniv Bordeaux 2, INRA, UMR Genom Divers & Pouvoir Pathogene, IBVM, BP81, Villenave Dornon, France
Cosson, Patrick
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Sofer, Luc
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Schurdi-Levraud, Valerie
Revers, Frederic
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Univ Bordeaux 2, INRA, UMR Genom Divers & Pouvoir Pathogene, IBVM, BP81, Villenave Dornon, FranceUniv Bordeaux 2, INRA, UMR Genom Divers & Pouvoir Pathogene, IBVM, BP81, Villenave Dornon, France
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Univ Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, FranceUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Cosson, Patrick
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Sofer, Luc
Le, Quang Hien
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Univ Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, FranceUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Le, Quang Hien
Leger, Valerie
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INRA, UMR BIOGECO 1202, Equipe Genet, F-33612 Cestas, FranceUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Leger, Valerie
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Schurdi-Levraud, Valerie
Whitham, Steven A.
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Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USAUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Whitham, Steven A.
Yamamoto, Miki L.
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Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USAUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Yamamoto, Miki L.
Gopalan, Suresh
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Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USAUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Gopalan, Suresh
Le Gall, Olivier
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Univ Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, FranceUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Le Gall, Olivier
Candresse, Thierry
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Univ Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, FranceUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Candresse, Thierry
Carrington, James C.
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Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USAUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France
Carrington, James C.
Revers, Frederic
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Univ Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, FranceUniv Bordeaux 2, INRA, UMR Genom Diversite & Pouvoir Pathogene, F-33883 Villenave Dornon, France