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Fig. 4. Foxa2 inhibits En2{Delta}SP binding to the HF1 and HF2 sites of MAP1B promoter. (A) Binding of En2{Delta}SP and Foxa2 to the HF1 site. The HF1 probe sequence, highlighting the ATTA (square box) and Foxa2 (oval box) sites, is represented above the EMSA panels. Purified En2{Delta}SP or GST-Foxa2 fusion proteins were incubated independently (lanes 2-7), or in combination (lanes 8-9). Lane 1: free HF1 probe; lanes 2-3: 25 and 50 ng of En2{Delta}SP, respectively; lanes 4-5 and 6-7 show two different autoradiographic exposures of the same gel area (4-5: long exposure; 6-7: short exposure). Gels were loaded with 40 ng (lanes 4 and 6) or 120 ng (lanes 5 and 7) of GST-Foxa2. An interaction of Foxa2 with HF1 is visible in lane 5 (double arrowhead). At low concentration (lane 2: 25 ng) En2{Delta}SP gives one retarded band, while at a higher one (lane 3: 50 ng) it generates two retarded bands (arrowheads). Co-incubation of GST-Foxa2 with En2{Delta}SP leads to an inhibition of En2{Delta}SP binding (compare lane 3 to lanes 8 and 9). (B) Binding test for En2{Delta}SP and Foxa2 to the HF2 site. The probe sequence, highlighting the ATTA (square box) and Foxa2 (oval box) sites, is represented above the EMSA panel. Purified En2{Delta}SP or GST-Foxa2 fusion protein were incubated independently (lane 2: 50, lane 3, 100 ng of En2{Delta}SP; lane 4: 120, lane 5, 200 ng of GST-Foxa2) or together (lane 6-9) with the HF2 probe. En2{Delta}SP was preincubated with HF2 for 20 minutes, before adding Foxa2. En2{Delta}SP binds HF2 (arrowhead), GST-Foxa2 does not bind by itself (lanes 4,5) but dissociates En2{Delta}SP from HF2 (compare lane 2 with lanes 6-7, and lane 3 with lanes 8-9).





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