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| 30 April 2001, Volume 20, Number 19, Pages 2378-2389 |
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| The mammalian Jun proteins: redundancy and specificity |
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| Fatima Mechta-Grigoriou, Damien Gerald and Moshe Yaniv |
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Unité des virus oncogenes, CNRS URA 1644, Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris Cedex 15, France
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Correspondence to: M Yaniv, Unité des virus oncogenes, CNRS URA 1644, Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris Cedex 15, France
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| Abstract |
 | The AP-1 transcription factor is composed of a mixture of homo- and hetero-dimers formed between Jun and Fos proteins. The different Jun and Fos family members vary significantly in their relative abundance and their interactions with additional proteins generating a complex network of transcriptional regulators. Thus, the functional activity of AP-1 in any given cell depends on the relative amount of specific Jun/Fos proteins which are expressed, as well as other potential interacting proteins. This diversity of AP-1 components has complicated our understanding of AP-1 function and resulted in a paucity of information about the precise role of individual AP-1 members in distinct cellular processes. We shall discuss recent studies which suggest that different Jun and Fos family members may have both opposite and overlapping functions in cellular proliferation and cell fate. Oncogene (2001) 20, 2378-2389. |
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| Keywords |
 | cell cycle; transcription; ras signaling; apoptosis |
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| 30 April 2001, Volume 20, Number 19, Pages 2378-2389 |
| Table of contents Previous Abstract Next Full text PDF |
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