Fig. 4.
Fig. 4. Interaction between the DRIP complex and the retinoid receptors in U937 clones that differ in their PML-RARα expression. / (A) Expression of RARα and fusion PML-RARα proteins in NB4 and U937 subclones by Western blot analysis. Twenty micrograms of the nuclear extracts were run on SDS-PAGE, transferred, and probed with an anti-RARα antibody recognizing its F domain. Positions of RARα and the fusion PML-RARα proteins are indicated. (B) Interaction of the DRIP/TRAP complex with retinoid receptors in U937 subclones (lanes 6-11), HL-60 cells (lanes 4, 5). (C) Direct interaction between the PML-RARα protein and the DRIP205. In vitro translated35S-labeled PML-RARα and mutant PML-RARα M4 were incubated with purified GST-DRIP205 in the absence (−) and presence (+) of 1 μmol/L or 10 μmol/L t-RA (lanes 3, 4, 7, 8). GST alone was included as the negative control (lanes 1, 5).

Interaction between the DRIP complex and the retinoid receptors in U937 clones that differ in their PML-RARα expression.

(A) Expression of RARα and fusion PML-RARα proteins in NB4 and U937 subclones by Western blot analysis. Twenty micrograms of the nuclear extracts were run on SDS-PAGE, transferred, and probed with an anti-RARα antibody recognizing its F domain. Positions of RARα and the fusion PML-RARα proteins are indicated. (B) Interaction of the DRIP/TRAP complex with retinoid receptors in U937 subclones (lanes 6-11), HL-60 cells (lanes 4, 5). (C) Direct interaction between the PML-RARα protein and the DRIP205. In vitro translated35S-labeled PML-RARα and mutant PML-RARα M4 were incubated with purified GST-DRIP205 in the absence (−) and presence (+) of 1 μmol/L or 10 μmol/L t-RA (lanes 3, 4, 7, 8). GST alone was included as the negative control (lanes 1, 5).

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