Cooperation between Ras effector loop mutants and cyclins in inducing anchorage-independent growth of NIH 3T3 cells
Cell line | Colony-forming efficiency (% ± SD)a | |||
---|---|---|---|---|
+pBabePuro | +Cyclin D1 | +Cyclin E | +Cyclin A | |
neo | 0 | 0 | 0 | 0 |
12V | 2.2 ± 0.1 | 12.1 ± 1.0 | 4.7 ± 0.5 | 5.1 ± 0.6 |
12V,35S | 0b | 1.0 ± 0.1 | 0.4 ± 0.1 | 2.0 ± 0.2 |
12V,37G | 0b | 2.5 ± 0.1 | 1.2 ± 0.1 | 1.7 ± 0.4 |
12V,40C | 0b | 1.7 ± 0.2 | 0b | 3.7 ± 0.3 |
↵a A total of 10,000 cells were seeded into 0.3% agar. Macroscopic colonies were scored after 2 weeks of growth. Each infection with cyclin-expressing viruses was performed twice; each pool of infectants was then analyzed twice in duplicate. Values represent averages of all determinations ± 1 standard deviation. See text for further details. +pBabePuro, cells infected with a retroviral vector lacking a cDNA insert; +cyclin D1, E, or A, cells infected with a retroviral vector that drives expression of a human cyclin of the indicated type.
↵b Formation of microscopic colonies (see footnote b to Table 1).