Abstract
We have transiently expressed a dominant negative form of rac1 (N17rac1) using adenoviral-mediated gene transfer. The level of N17rac1 expression is demonstrated to be proportional to the multiplicity of infection. Expression of N17rac1 in Rat 2 fibroblasts results in cytostatic growth arrest. Cell-cycle analysis demonstrates that cells expressing N17rac1 accumulate in G2/M. These results suggest that rac1 is required for cell proliferation and provide the first demonstration in mammalian cells of a role for small GTP-binding proteins in the G2/M transition.
Original language | English (US) |
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Pages (from-to) | 17-20 |
Number of pages | 4 |
Journal | Biochemical Journal |
Volume | 326 |
Issue number | 1 |
State | Published - Aug 15 1997 |
Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry