Autor: | Olivia Furstoss, Marc Piechaczyk, Isabelle Jariel-Encontre, Ann-Muriel Steff, Catherine Salvat, Claire Acquaviva, Magali Pariat |
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Rok vydání: | 1997 |
Předmět: |
0303 health sciences
biology c-jun Context (language use) Calpain General Medicine c-Fos 03 medical and health sciences 0302 clinical medicine Proteasome Biochemistry Ubiquitin In vivo 030220 oncology & carcinogenesis Genetics biology.protein Molecular Biology Transcription factor 030304 developmental biology |
Zdroj: | Molecular Biology Reports. 24:51-56 |
ISSN: | 0301-4851 |
DOI: | 10.1023/a:1006804723722 |
Popis: | c-fos and c-jun proto-oncogenes have originally been found in mutated forms in murine and avian oncogenic retroviruses. They both define multigenic families of transcription factors. Both c-jun and c-fos proteins are metabolically unstable. In vivo and in vitro work by various groups suggests that multiple proteolytic machineries, including the lysosomes, the proteasome and the ubiquitous calpains, may participate in the destruction of c-fos and c-jun. The relative contribution of each pathway is far from being known and it cannot be excluded that it varies according to the cell context and/or the physiological conditions. It has been demonstrated that, in certain occurrences, the degradation of both c-fos and c-jun by the proteasome in vivo involves the ubiquitin pathway. However, the possibility that proteasomal degradation can also occur in a manner independent of the E1 enzyme of the ubiquitin cycle remains an open issue. |
Databáze: | OpenAIRE |
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