Fig. 5.
Fig. 5. Activation of Py replicon by GAL4–STAT fusion protein. / (A) Schematic diagram of GAL4–STAT fusion proteins used. (B) GAL4–STAT5A or GAL4–STAT5B was transfected with Py LTag and pPyG5OICAT, which contains a 5-tandem repeat of GAL4 binding site and Py replication origin, into BA/F3 cells. After 24 hours of culture, replication was analyzed by DpnI assay. The replicatedDpnI-resistant plasmid is indicated by the arrow. (C) The indicated doses of GAL4–STAT5 or its mutants were transfected with SRα-LTag and pPyG5OICAT into BA/F-wild cells. After 24 hours of stimulation, DpnI assay was done.

Activation of Py replicon by GAL4–STAT fusion protein.

(A) Schematic diagram of GAL4–STAT fusion proteins used. (B) GAL4–STAT5A or GAL4–STAT5B was transfected with Py LTag and pPyG5OICAT, which contains a 5-tandem repeat of GAL4 binding site and Py replication origin, into BA/F3 cells. After 24 hours of culture, replication was analyzed by DpnI assay. The replicatedDpnI-resistant plasmid is indicated by the arrow. (C) The indicated doses of GAL4–STAT5 or its mutants were transfected with SRα-LTag and pPyG5OICAT into BA/F-wild cells. After 24 hours of stimulation, DpnI assay was done.

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