Literature DB >> 8756277

The limb field mesoderm determines initial limb bud anteroposterior asymmetry and budding independent of sonic hedgehog or apical ectodermal gene expressions.

M A Ros1, A López-Martínez, B K Simandl, C Rodriguez, J C Izpisúa Belmonte, R Dahn, J F Fallon.   

Abstract

We have analyzed the pattern of expression of several genes implicated in limb initiation and outgrowth using limbless chicken embryos. We demonstrate that the expressions of the apical ridge associated genes, Fgf-8, Fgf-4, Bmp-2 and Bmp-4, are undetectable in limbless limb bud ectoderm; however, FGF2 protein is present in the limb bud ectoderm. Shh expression is undetectable in limbless limb bud mesoderm. Nevertheless, limbless limb bud mesoderm shows polarization manifested by the asymmetric expression of Hoxd-11, -12 and -13, Wnt-5a and Bmp-4 genes. The posterior limbless limb bud mesoderm, although not actually expressing Shh, is competent to express it if supplied with exogenous FGF or transplanted to a normal apical ridge environment, providing further evidence of mesodermal asymmetry. Exogenous FGF applied to limbless limb buds permits further growth and determination of recognizable skeletal elements, without the development of an apical ridge. However, the cells competent to express Shh do so at reduced levels; nevertheless, Bmp-2 is then rapidly expressed in the posterior limbless mesoderm. limbless limb buds appear as bi-dorsal structures, as the entire limb bud ectoderm expresses Wnt-7a, a marker for dorsal limb bud ectoderm; the ectoderm fails to express En-1, a marker of ventral ectoderm. As expected, C-Lmx1, which is downstream of Wnt-7a, is expressed in the entire limbless limb bud mesoderm. We conclude that anteroposterior polarity is established in the initial limb bud prior to Shh expression, apical ridge gene expression or dorsal-ventral asymmetry. We propose that the initial pattern of gene expressions in the emergent limb bud is established by axial influences on the limb field. These permit the bud to emerge with asymmetric gene expression before Shh and the apical ridge appear. We report that expression of Fgf-8 by the limb ectoderm is not required for the initiation of the limb bud. The gene expressions in the pre-ridge limb bud mesoderm, as in the limb bud itself, are unstable without stimulation from the apical ridge and the polarizing region (Shh) after budding is initiated. We propose that the defect in limbless limb buds is the lack of a dorsal-ventral interface in the limb bud ectoderm where the apical ridge induction signal would be received and an apical ridge formed. These observations provide evidence for the hypothesis that the dorsal-ventral ectoderm interface is a precondition for apical ridge formation.

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Year:  1996        PMID: 8756277     DOI: 10.1242/dev.122.8.2319

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  13 in total

1.  Two lineage boundaries coordinate vertebrate apical ectodermal ridge formation.

Authors:  R A Kimmel; D H Turnbull; V Blanquet; W Wurst; C A Loomis; A L Joyner
Journal:  Genes Dev       Date:  2000-06-01       Impact factor: 11.361

2.  Oriented cell motility and division underlie early limb bud morphogenesis.

Authors:  Laurie A Wyngaarden; Kevin M Vogeli; Brian G Ciruna; Mathew Wells; Anna-Katerina Hadjantonakis; Sevan Hopyan
Journal:  Development       Date:  2010-06-16       Impact factor: 6.868

3.  Expression of Sonic hedgehog gene in regenerating newt limb blastemas recapitulates that in developing limb buds.

Authors:  Y Imokawa; K Yoshizato
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

Review 4.  Ectoderm-mesoderm crosstalk in the embryonic limb: The role of fibroblast growth factor signaling.

Authors:  Francesca V Mariani; Marian Fernandez-Teran; Maria A Ros
Journal:  Dev Dyn       Date:  2017-02-06       Impact factor: 3.780

5.  Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1.

Authors:  Terence D Capellini; Giulia Vaccari; Elisabetta Ferretti; Sebastian Fantini; Mu He; Massimo Pellegrini; Laura Quintana; Giuseppina Di Giacomo; James Sharpe; Licia Selleri; Vincenzo Zappavigna
Journal:  Development       Date:  2010-08-01       Impact factor: 6.868

6.  Fgf8 is required for outgrowth and patterning of the limbs.

Authors:  A M Moon; M R Capecchi
Journal:  Nat Genet       Date:  2000-12       Impact factor: 38.330

7.  Wnt3a-/--like phenotype and limb deficiency in Lef1(-/-)Tcf1(-/-) mice.

Authors:  J Galceran; I Fariñas; M J Depew; H Clevers; R Grosschedl
Journal:  Genes Dev       Date:  1999-03-15       Impact factor: 11.361

8.  Identification of spontaneous mutations within the long-range limb-specific Sonic hedgehog enhancer (ZRS) that alter Sonic hedgehog expression in the chicken limb mutants oligozeugodactyly and silkie breed.

Authors:  Sarah A Maas; Takayuki Suzuki; John F Fallon
Journal:  Dev Dyn       Date:  2011-05       Impact factor: 3.780

Review 9.  Vertebrate limb development: moving from classical morphogen gradients to an integrated 4-dimensional patterning system.

Authors:  Jean-Denis Bénazet; Rolf Zeller
Journal:  Cold Spring Harb Perspect Biol       Date:  2009-10       Impact factor: 10.005

10.  Spatiotemporal regulation of GLI target genes in the mammalian limb bud.

Authors:  Jordan P Lewandowski; Fang Du; Shilu Zhang; Marian B Powell; Kristin N Falkenstein; Hongkai Ji; Steven A Vokes
Journal:  Dev Biol       Date:  2015-07-31       Impact factor: 3.582

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