Since the discovery of v-jun as the transforming protein of the sarcom
a virus 17 three mammalian homologues of v-jun have been isolated. All
three jun genes respond to a multitude of agents, and the encoded pro
teins in turn bind to and regulate, positively or negatively, the tran
scription of dependent genes, thereby influencing cellular fate. In ad
dition, through transcription factor ''cross-talk'' Jun influences the
transcription of genes regulated by different classes of transcriptio
n factors, such as steroid hormone receptors. Although the role of Jun
proteins in transcriptional regulation has been thoroughly analyzed i
n recent years, the role of Jun proteins in oncogenesis is still poorl
y understood.