Literature DB >> 9507106

Zebrafish wnt11: pattern and regulation of the expression by the yolk cell and No tail activity.

R Makita1, T Mizuno, S Koshida, A Kuroiwa, H Takeda.   

Abstract

This study analyzed the spatial and temporal expression pattern of zebrafish wnt11 and the regulation of the expression during zebrafish early development, focusing on the interaction with the no tail (ntl) gene, a zebrafish orthologue of mouse Brachyury (T). Zygotic expression of wnt11 was first detected at the late blastula stage in the blastoderm margin, a presumptive mesoderm region. wnt11 expression coincided with mesoderm induction, and the expression was induced by mesoderm inducers such as the yolk cell (Mizuno, T., Yamaha, E., Wakahara, M., Kuroiwa, A., Takeda, H., 1996. Mesoderm induction in zebrafish. Nature 383, 131-132) or FGFs, indicating that, like ntl, wnt11 is one of the immediate-early genes in mesoderm induction. Initial expression domains of wnt11 and ntl overlapped, and these genes showed a similar response to mesoderm inducers. However, analysis of the ntl mutant embryos suggested that wnt11 and ntl are placed in distinct genetic pathways; the ntl mutation had no effect on wnt11 expression in the blastoderm margin. This was further supported by the result of RNA injection experiments showing that overexpression of Wnt11 did not affect ntl expression in the margin. Thus, wnt11 and ntl expression are induced and maintained independently in their initial phase of expression. In later stages, wnt11 was expressed in various organs, such as the somites, particularly in the developing notochord. Since no wnt gene has been reported to be expressed in the axial mesoderm, which is known to act as a signaling source that patterns the neural tube and somites, zebrafish wnt11 is the first wnt gene expressed in the notochord. Furthermore, in contrast to early expression, wnt11 expression in the notochord depended on Ntl activity. In the ntl mutant in which somite patterning is severely affected, wnt11 expression was completely lost, while another signaling molecule, sonic hedgehog is expressed in the mutant notochord precursor cells (Krauss, S., Concordet, J.-P., Ingham, P.W., 1993. A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos. Cell 75, 1431-1444). wnt11 expression in the somite also shows a characteristic pattern, correlated with the migration and differentiation of slow muscle precursors. These observations suggest a role for wnt11 in patterning the somites.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9507106     DOI: 10.1016/s0925-4773(98)00013-6

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  19 in total

1.  Nerve growth factor regulates axial rotation during early stages of chick embryo development.

Authors:  Annalisa Manca; Simona Capsoni; Anna Di Luzio; Domenico Vignone; Francesca Malerba; Francesca Paoletti; Rossella Brandi; Ivan Arisi; Antonino Cattaneo; Rita Levi-Montalcini
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-25       Impact factor: 11.205

2.  Identification and mechanism of regulation of the zebrafish dorsal determinant.

Authors:  Fu-I Lu; Christine Thisse; Bernard Thisse
Journal:  Proc Natl Acad Sci U S A       Date:  2011-09-12       Impact factor: 11.205

3.  Lzts2 regulates embryonic cell movements and dorsoventral patterning through interaction with and export of nuclear β-catenin in zebrafish.

Authors:  Yuanyuan Li; Qing Li; Yong Long; Zongbin Cui
Journal:  J Biol Chem       Date:  2011-11-04       Impact factor: 5.157

4.  Tbx2b is required for the development of the parapineal organ.

Authors:  Corey D Snelson; Kirankumar Santhakumar; Marnie E Halpern; Joshua T Gamse
Journal:  Development       Date:  2008-04-02       Impact factor: 6.868

5.  Slb/Wnt11 controls hypoblast cell migration and morphogenesis at the onset of zebrafish gastrulation.

Authors:  Florian Ulrich; Miguel L Concha; Paul J Heid; Ed Voss; Sabine Witzel; Henry Roehl; Masazumi Tada; Stephen W Wilson; Richard J Adams; David R Soll; Carl-Philipp Heisenberg
Journal:  Development       Date:  2003-09-16       Impact factor: 6.868

6.  No tail co-operates with non-canonical Wnt signaling to regulate posterior body morphogenesis in zebrafish.

Authors:  Florence Marlow; Encina M Gonzalez; Chunyue Yin; Concepcion Rojo; Lilianna Solnica-Krezel
Journal:  Development       Date:  2003-12-03       Impact factor: 6.868

7.  Knockdown of a galectin-1-like protein in zebrafish (Danio rerio) causes defects in skeletal muscle development.

Authors:  Hafiz Ahmed; Shao-J Du; Gerardo R Vasta
Journal:  Glycoconj J       Date:  2008-09-02       Impact factor: 2.916

8.  Csrp1 regulates dynamic cell movements of the mesendoderm and cardiac mesoderm through interactions with Dishevelled and Diversin.

Authors:  Kota Y Miyasaka; Yasuyuki S Kida; Takayuki Sato; Mari Minami; Toshihiko Ogura
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-25       Impact factor: 11.205

9.  A gene regulatory network directed by zebrafish No tail accounts for its roles in mesoderm formation.

Authors:  Rosalind H Morley; Kim Lachani; Damian Keefe; Michael J Gilchrist; Paul Flicek; James C Smith; Fiona C Wardle
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-18       Impact factor: 11.205

10.  Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1.

Authors:  Sarah H Louie; Xiao Yong Yang; William H Conrad; Jeanot Muster; Stephane Angers; Randall T Moon; Benjamin N R Cheyette
Journal:  PLoS One       Date:  2009-02-02       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.