“…In zebrafish, mutations in the Pax2.1 gene (no isthmus or noi) and in the Fgf8 gene (acerebellar or ace) disrupt MHB development (Brand et al, 1996). When formed, the MHB displays organizer activities (Marin and Puelles, 1994;Martinez et al, 1991), generating signals that induce the development of cerebellum, tegmentum, and optic tectum. wnt1 mutations in mouse disrupt MHB development (McMahon and Bradley, 1990;McMahon et al, 1992;Thomas and Capecchi, 1990;Thomas et al, 1991), and wnt1 distributions suggest a similar role in MHB formation in zebrafish (Kelly and Moon, 1995), but mutations in the zebrafish wnt1 gene have not been identified.…”