Lekven, Arne C2015-12-012017-04-072015-12-012017-04-072013-122013-10-04http://hdl.handle.net/1969.1/151622Vertebrate dorsoventral patterning requires both Wnt8 and BMP signaling. Because of their multiple interactions, discerning roles attributable specifically to Wnt8 independent of BMP has been a challenge. For example, Wnt8 represses the dorsal organizer that negatively regulates ventral BMP signals, thus Wnt8 loss-of-function phenotypes may reflect the combined effects of reduced Wnt8 and BMP signaling. We have taken a loss-of-function approach in the zebrafish to generate embryos lacking expression of both Wnt8 and the BMP antagonist Chordin. wnt8;chordin loss-of-function embryos show rescued BMP signaling, thereby allowing us to identify Wnt8-specific requirements. Our analysis shows that Wnt8 is uniquely required to repress prechordal plate specification but not notochord, and that Wnt8 signaling is not essential for specification of tailbud progenitors but is required for normal expansion of posterior mesoderm cell populations. Further, we find that Wnt8 is required for the normal expression of cdx4 and ntl, but not wnt3a. Finally, we find that Wnt8 is required for cell proliferation in the tailbud. Thus, Wnt8 and BMP signaling have independent roles during ertebrate ventrolateral mesoderm development that can be identified through loss-of-function analysis.enWnt8posterior developmentpatterningembryoThesis