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. 1998 Apr 15;12(8):1227–1239. doi: 10.1101/gad.12.8.1227

Table 1.

Anchorage-independent growth of CEF-expressing c-Jun and v-Jun bZip mutants

Culture
Number of cells seededa
Plating efficiency (%)
1 × 104
2 × 103
1 × 103
Uninfected
R vector
R–c-Jun wild type + 444/442 222/168 21
R–c-Jun-m0 + 198/258 142/108 13
R–c-Jun-m1 92/86* 26/23# <1
R–v-Jun + 550/496 142/164 19.5
R–v-Jun–m0 + 210/178 102/88  9.6
R–v-Jun–m1 24/32* 10/14* 4/8* <1
R–Fra2 +** 52/32** 14/16** 1.8
R–ATF2
RD–v-Jun–m1 +  R vector 16/12* N.D.
RD–v-Jun–m1 +  R–v-Jun–m0 N.D. 64/44 N.D.
RD–v-Jun–m0 +  R vector N.D. 194/220 N.D.
RD–v-Jun–m0 +  R–v-Jun–ml N.D. 398/346 N.D.

Colony formation in agar of CEF cultures fully infected with the retroviruses indicated. Duplicates were seeded on 60-mm plates at the densities indicated, and colonies were scored after 2 weeks. 

a

Plating efficiency: percentage of single cells of 1 × 103 developing into colonies. (+) Numerous colonies; (−) no colonies present; (*) many colonies show necroses; (**) microcolonies; (N.D.) not determined.