The C-terminal domain of Orc6 is essential for interaction with Pnut protein and cell division. (A) His-tagged purified Drosophila WT Orc6 protein (HisOrc6, lane 2) and Orc6 mutant proteins (HisOrc6–224, lane 3, and HisOrc6–200, lane 4) were incubated with Drosophila L2 extracts. Precipitated with cobalt beads, material was analyzed for presence of Pnut protein during immunoblot experiment with α-Pnut antibody. No recombinant protein was added in lane 5; 1 μl of L2 extract was loaded on lane 1. Lane 6 shows Pnut protein precipitated from L2 extract by antibody raised against Drosophila Orc6 protein. (B) Orc6–200 deletion mutant protein does not localize to cell membrane in L2 cells after overexpression. L2 cells expressing recombinant GFP fusions of Orc6-WT and Orc6–200 deletion mutant are presented. (C) Overexpression of Orc6–200 causes the formation of multinucleated cells, which are still able to incorporate BrdUrd. Cells were labeled with BrdUrd for 20 h after transfection with the GFP-fusion Orc6–200 mutant protein and stained with anti-BrdUrd antibody. Presented images show the GFP signal, BrdUrd incorporation, DAPI staining, and DIC images from left to right. These data and those with other mutants are presented quantitatively in .