Details

Autor(en) / Beteiligte

• Johnson, David G.
• Cress, W. Douglas
• Jakoi, Laszlo
• Nevins, Joseph R.

Titel

Oncogenic Capacity of the E2F1 Gene

Ist Teil von

• Proceedings of the National Academy of Sciences - PNAS, 1994-12, Vol.91 (26), p.12823-12827

Ort / Verlag

United States: National Academy of the Sciences of the United States of America

Erscheinungsjahr

1994

Quelle

Electronic Journals Library

Beschreibungen/Notizen

• Previous experiments have identified the E2F transcription factor as a potential downstream target for the action of cellular regulatory activities, such as the Rb tumor suppressor protein, that control cell growth and that, when altered, contribute to the development of human tumors. In light of these findings, we have assayed the ability of the E2F1 and DP1 genes, which encode heterodimeric partners that together create E2F activity, to act in an oncogenic fashion. We find that E2F1, particularly in combination with the DP1 product, cooperates with an activated ras oncogene to induce the formation of morphologically transformed foci in primary rat embryo fibroblast cultures. In addition, an E2F1 chimeric protein, in which sequences involved in Rb binding have been replaced with the herpesvirus VP16 activation domain, exhibits increased transformation activity. Cells transfected with E2F1 and DP1 or the E2F1-VP16 chimera form colonies in soft agar and induce tumor formation in nude mice. We conclude that deregulated E2F1 expression and function can have oncogenic consequences.