Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Dev Biol June 1, 2007; 306 (1): 160-9.

The secreted EGF-Discoidin factor xDel1 is essential for dorsal development of the Xenopus embryo.

Arakawa A , Matsuo-Takasaki M , Takai A , Inomata H , Matsumura M , Ikeya M , Takahashi K , Miyachi Y , Sasai N , Sasai Y .

We show here that a secreted EGF-Discoidin-domain protein, Xenopus Del1 (xDel1), is an essential factor for dorsal development in the early Xenopus embryo. Knockdown of the xDel1 function causes obvious ventralization of the embryo. Conversely, overexpression of xDel1 expands dorsal-marker expression and suppresses ventral-marker expression in the gastrula embryo. Forced expression of xDel1 dorsalizes ventral marginal zone explants, whereas it weakly induces neural differentiation but not mesodermal differentiation in animal caps. The dorsalizing activity of xDel1 is dependent on the Discoidin domains and not on the RGD motif (which is implicated in its angiogenic activity) or EGF repeats. Luciferase assays show that xDel1 attenuates BMP-signaling reporter activity by interfering with the pathway downstream of the BMP receptor. Thus, xDel1 functions as a unique extracellular regulatory factor of DV patterning in early vertebrate embryogenesis.

PubMed ID: 17433289
Article link: Dev Biol

Genes referenced: babam2 bmp4 chrd.1 edil3 egf gsc smad2 smad6 szl tbxt ventx1.2 wnt8a
Morpholinos: chrd MO1 chrd MO2 edil3 MO2 edil3 MO3

Article Images: [+] show captions

Xenbase: The Xenopus laevis and X. tropicalis resource.
Version: 4.12.0

Major funding for Xenbase is provided by grant P41 HD064556