Physical interaction between GATA-4 and SRF is mediated by the second zinc finger and the immediate C-terminal basic region. In vitro-translated [35S]methionine-labeled wild-type (WT) GATA-4 (lanes 1 to 3), an N-terminally truncated GATA-4 (ΔN) (lanes 4 to 6), both zinc fingers of GATA-4 (ZF1 + ZF2) (lanes 7 to 9), N-terminal GATA-4 with a deletion of ZF1 (ΔN + ΔZF1) (lanes 10 to 12), the first zinc finger of GATA-4 (ZF1) (lanes 13 to 15), and the second zinc finger along with the immediate C-terminal basic region of GATA-4 (ZF2) (lanes 16 to 18) (7.5 μl each) were incubated with approximately 1 μg (lanes 2, 5, 8, 11, 14, and 17) of GST or GST-SRF fusion protein (lanes 3, 6, 9, 12, 15, and 18) immobilized on glutathione-agarose beads. The beads were washed extensively, and the bound proteins were resolved on an SDS–10% protein gel and visualized by autoradiography. For lanes 1, 4, 7, 10, and 16, 0.75-μl volumes of the lysates were run.