|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720-3202, USA
*Author for correspondence (e-mail: harland{at}socrates.berkeley.edu)
Accepted 11 April 2002
Derrière is a recently discovered member of the TGFß superfamily that can induce mesoderm in explant assays and is expressed at the right time and location to mediate mesoderm induction in response to VegT during Xenopus embryogenesis. We show that the ability of Derrière to induce dorsal or ventral mesoderm depends strictly on the location of expression and that a dominant-negative Derrière cleavage mutant completely blocks all mesoderm formation when ectopically expressed. This differs from the activity of similar Xnr2 cleavage mutant constructs, which are secreted and retain signaling activity. Additional analysis of mesoderm induction by Derrière and members of the Nodal family indicates that these molecules are involved in a mutual positive-feedback loop and antagonism of either one of the signals can reduce the other. Interaction between Derrière and members of the Nodal family is also shown to occur through the formation of heterodimeric ligands. Using an oocyte expression system we show direct interaction between the mature Derrière ligand and members of both the Nodal and BMP families. Taken together, these findings indicate that Derrière and Nodal proteins probably work cooperatively to induce mesoderm throughout the marginal zone during early Xenopus development.
Key words: BMP, Bone morphogenetic protein, Derrière, Nodal, Xnr, Proteolytic processing, Cerberus, Dominant negative, Heterodimer, Mesoderm induction, Xenopus laevis
This article has been cited by other articles:
![]() |
C. Chang and R. M. Harland Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation Development, November 1, 2007; 134(21): 3861 - 3872. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Wang and B. K Tsang Nodal signalling and apoptosis Reproduction, May 1, 2007; 133(5): 847 - 853. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. M. Shen Nodal signaling: developmental roles and regulation Development, March 15, 2007; 134(6): 1023 - 1034. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Ogawa, A. Saito, H. Matsui, H. Suzuki, S. Ohtsuka, D. Shimosato, Y. Morishita, T. Watabe, H. Niwa, and K. Miyazono Activin-Nodal signaling is involved in propagation of mouse embryonic stem cells J. Cell Sci., January 1, 2007; 120(1): 55 - 65. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Sopory, S. M. Nelsen, C. Degnin, C. Wong, and J. L. Christian Regulation of Bone Morphogenetic Protein-4 Activity by Sequence Elements within the Prodomain J. Biol. Chem., November 10, 2006; 281(45): 34021 - 34031. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Wang, J.-Y. Jiang, C. Zhu, C. Peng, and B. K. Tsang Role and Regulation of Nodal/Activin Receptor-Like Kinase 7 Signaling Pathway in the Control of Ovarian Follicular Atresia Mol. Endocrinol., October 1, 2006; 20(10): 2469 - 2482. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Chen, S. M. Ware, A. Sato, D. E. Houston-Hawkins, R. Habas, M. M. Matzuk, M. M. Shen, and C. W. Brown The Vg1-related protein Gdf3 acts in a Nodal signaling pathway in the pre-gastrulation mouse embryo Development, January 15, 2006; 133(2): 319 - 329. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Birsoy, L. Berg, P. H. Williams, J. C. Smith, C. C. Wylie, J. L. Christian, and J. Heasman XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGF{beta} proteins in Xenopus development Development, February 1, 2005; 132(3): 591 - 602. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Xu, Y. Zhong, S. Munir, B. B. Yang, B. K. Tsang, and C. Peng Nodal Induces Apoptosis and Inhibits Proliferation in Human Epithelial Ovarian Cancer Cells via Activin Receptor-Like Kinase 7 J. Clin. Endocrinol. Metab., November 1, 2004; 89(11): 5523 - 5534. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Degnin, F. Jean, G. Thomas, and J. L. Christian Cleavages within the Prodomain Direct Intracellular Trafficking and Degradation of Mature Bone Morphogenetic Protein-4 Mol. Biol. Cell, November 1, 2004; 15(11): 5012 - 5020. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Piepenburg, D. Grimmer, P. H. Williams, and J. C. Smith Activin redux: specification of mesodermal pattern in Xenopus by graded concentrations of endogenous activin B Development, October 15, 2004; 131(20): 4977 - 4986. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Munir, G. Xu, Y. Wu, B. Yang, P. K. Lala, and C. Peng Nodal and ALK7 Inhibit Proliferation and Induce Apoptosis in Human Trophoblast Cells J. Biol. Chem., July 23, 2004; 279(30): 31277 - 31286. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. J. Sadlon, I. D. Lewis, and R. J. D'Andrea BMP4: Its Role in Development of the Hematopoietic System and Potential as a Hematopoietic Growth Factor Stem Cells, July 1, 2004; 22(4): 457 - 474. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. W. Harms and C. Chang Tomoregulin-1 (TMEFF1) inhibits nodal signaling through direct binding to the nodal coreceptor Cripto Genes & Dev., November 1, 2003; 17(21): 2624 - 2629. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Yokota, M. Kofron, M. Zuck, D. W. Houston, H. Isaacs, M. Asashima, C. C. Wylie, and J. Heasman A novel role for a nodal-related protein; Xnr3 regulates convergent extension movements via the FGF receptor Development, May 15, 2003; 130(10): 2199 - 2212. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. M. Rosa Cripto, a Multifunctional Partner in Signaling: Molecular Forms and Activities Sci. Signal., November 12, 2002; 2002(158): pe47 - pe47. [Abstract] [Full Text] [PDF] |
||||