Literature DB >> 26249743

How the embryo makes a limb: determination, polarity and identity.

Cheryll Tickle1.   

Abstract

The vertebrate limb with its complex anatomy develops from a small bud of undifferentiated mesoderm cells encased in ectoderm. The bud has its own intrinsic polarity and can develop autonomously into a limb without reference to the rest of the embryo. In this review, recent advances are integrated with classical embryology, carried out mainly in chick embryos, to present an overview of how the embryo makes a limb bud. We will focus on how mesoderm cells in precise locations in the embryo become determined to form a limb and express the key transcription factors Tbx4 (leg/hindlimb) or Tbx5 (wing/forelimb). These Tbx transcription factors have equivalent functions in the control of bud formation by initiating a signalling cascade involving Wnts and fibroblast growth factors (FGFs) and by regulating recruitment of mesenchymal cells from the coelomic epithelium into the bud. The mesoderm that will form limb buds and the polarity of the buds is determined with respect to both antero-posterior and dorso-ventral axes of the body. The position in which a bud develops along the antero-posterior axis of the body will also determine its identity - wing/forelimb or leg/hindlimb. Hox gene activity, under the influence of retinoic acid signalling, is directly linked with the initiation of Tbx5 gene expression in the region along the antero-posterior axis of the body that will form wings/forelimbs and determines antero-posterior polarity of the buds. In contrast, Tbx4 expression in the regions that will form legs/hindlimbs is regulated by the homeoprotein Pitx1 and there is no evidence that Hox genes determine antero-posterior polarity of the buds. Bone morphogenetic protein (BMP) signalling determines the region along the dorso-ventral axis of the body in which both wings/forelimbs and legs/hindlimbs develop and dorso-ventral polarity of the buds. The polarity of the buds leads to the establishment of signalling regions - the dorsal and ventral ectoderm, producing Wnts and BMPs, respectively, the apical ectodermal ridge producing fibroblast growth factors and the polarizing region, Sonic hedgehog (Shh). These signals are the same in both wings/forelimbs and legs/hindlimbs and control growth and pattern formation by providing the mesoderm cells of the limb bud as it develops with positional information. The precise anatomy of the limb depends on the mesoderm cells in the developing bud interpreting positional information according to their identity - determined by Pitx1 in hindlimbs - and genotype. The competence to form a limb extends along the entire antero-posterior axis of the trunk - with Hox gene activity inhibiting the formation of forelimbs in the interlimb region - and also along the dorso-ventral axis.
© 2015 Anatomical Society.

Entities:  

Keywords:  Hox genes; Pitx1; Sonic hedgehog; Tbx4/5; Wnts; antero-posterior polarity; apical ectodermal ridge; bone morphogenetic proteins; dorso-ventral polarity; embryo; fibroblast growth factors; lateral plate mesoderm; limb; limb bud; polarizing region; retinoic acid

Mesh:

Substances:

Year:  2015        PMID: 26249743      PMCID: PMC4580101          DOI: 10.1111/joa.12361

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  105 in total

Review 1.  Patterning the limb before and after SHH signalling.

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2.  Ectodermal Wnt3/beta-catenin signaling is required for the establishment and maintenance of the apical ectodermal ridge.

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Journal:  Genes Dev       Date:  2003-02-01       Impact factor: 11.361

3.  Hox9 genes and vertebrate limb specification.

Authors:  M J Cohn; K Patel; R Krumlauf; D G Wilkinson; J D Clarke; C Tickle
Journal:  Nature       Date:  1997-05-01       Impact factor: 49.962

4.  Islet1 regulates establishment of the posterior hindlimb field upstream of the Hand2-Shh morphoregulatory gene network in mouse embryos.

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6.  Dorso-ventral ectodermal compartments and origin of apical ectodermal ridge in developing chick limb.

Authors:  M Altabef; J D Clarke; C Tickle
Journal:  Development       Date:  1997-11       Impact factor: 6.868

7.  Retinoic acid application to chick wing buds leads to a dose-dependent reorganization of the apical ectodermal ridge that is mediated by the mesenchyme.

Authors:  C Tickle; A Crawley; J Farrar
Journal:  Development       Date:  1989-08       Impact factor: 6.868

8.  The role of Engrailed in establishing the dorsoventral axis of the chick limb.

Authors:  C Logan; A Hornbruch; I Campbell; A Lumsden
Journal:  Development       Date:  1997-06       Impact factor: 6.868

9.  Hox genes and the evolution of vertebrate axial morphology.

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Journal:  PLoS Genet       Date:  2014-08-28       Impact factor: 5.917

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6.  Development of the Proximal-Anterior Skeletal Elements in the Mouse Hindlimb Is Regulated by a Transcriptional and Signaling Network Controlled by Sall4.

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7.  The transcription factor NKX2-3 mediates p21 expression and ectodysplasin-A signaling in the enamel knot for cusp formation in tooth development.

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Review 8.  Appendages and gene regulatory networks: Lessons from the limbless.

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Review 9.  Postaxial limb hypoplasia (PALH): the classification, clinical features, and related developmental biology.

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10.  Widespread diversity in the transcriptomes of functionally divergent limb tendons.

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