You have designed a new beta-galactosidase reporter gene that contains the 3’ UTR of the maternal hunchback (mhb) transcript (A). When expressed in wild type embryos, you observe that the reporter gene is excluded from the germ cells, located in the posterior-most end (A). You then create a mutated version of this construct, with a 3'UTR lacking the Nanos Response Element (NRE) (B). When this construct is expressed in wild type embryos, the reporter gene is expressed in the germ cells (B). Finally, you replace the entire 3'UTR with the 3'UTR from the cell cycle gene, CyclinB (C). You find that the reporter gene is not expressed in the germ cells. 1) What do these results suggest about how nanos controls cyclin B expression? 2) Design an experiment to test this idea.