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Identification of calcium‐inducible genes in primary keratinocytes using suppression‐subtractive hybridization
Author(s) -
Seo EunYoung,
Lee WoongHee,
Piao YongJun,
Kim KyoungHoon,
Lee KyuMi,
Ahn KwangSung,
Yang JunMo,
Seo YoungJoon,
Kim Chang Deok,
Park JangKyu,
Lee JeungHoon
Publication year - 2004
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.0906-6705.2004.0144.x
Subject(s) - suppression subtractive hybridization , keratinocyte , biology , keratin , microbiology and biotechnology , northern blot , involucrin , cellular differentiation , gene , gene expression , genetics , in vitro , cdna library
Abstract: Terminal differentiation in epidermal keratinocytes involves major biochemical changes including the expression of many new differentiation‐specific genes. To further understand this process, we performed suppression‐subtractive hybridization of keratinocytes cultured under high‐calcium condition, known to induce differentiation in vitro . We randomly isolated 300 clones representing 90 different genes. By reverse Northern blot analyses, 20 different genes were found to be overexpressed, of which 13 were confirmed as differentially expressed genes during keratinocyte differentiation by Northern blot analysis. Of those, five genes, transglutaminase 1, keratin 6, interleukin‐1 receptor antagonist, kallikrein 7, and heat shock protein 27, are known to be up‐regulated during epidermal differentiation. Six genes, ferritin‐L chain, ribosomal protein S6, tumor‐associated calcium signal transducer 2, neuroendocrine secretory protein 55, phosphoserine aminotransferase, and neutrophil gelatinase‐associated lipocalin, heretofore were not known to be up‐regulated during keratinocyte differentiation. We also identified two novel genes. One of these maps to chromosome 1q21 of the epidermal differentiation complex, and its expression level was strongly increased in differentiating keratinocytes. These differentially expressed genes may provide significant opportunities for further understanding of the epidermal keratinocyte differentiation.