Literature DB >> 10642789

Plasticity of axial identity among somites: cranial somites can generate vertebrae without expressing Hox genes appropriate to the trunk.

R Kant1, R S Goldstein.   

Abstract

Classic studies have shown that the presomitic mesoderm is already committed to a specific morphological fate, for example, the ability to generate a rib. Hox gene expression in the paraxial mesoderm has also been shown to be fixed early and not susceptible to modulation by an ectopic environment. This is in contrast to the plasticity of Hox expression in neuroectodermal derivatives. We reexamine here the potential of somites for morphological plasticity by transplanting the cranial (occipital) somites 1-4, that normally produce small contributions to the skull, to the trunk of avian embryos. Surprisingly, the transposed cranial somites are able to form reasonably normal vertebral anlage. In addition, the cranial somitic mesoderm produces intervertebral disks, structures not normally found in the skull. These somites are however unable to generate some elements of the vertebrae, such as the costal process. In contrast to the morphogenetic plasticity of the occipital somites, their characteristic inability to support survival of dorsal root ganglia was not significantly modified by posterior transplantation. Dorsal root ganglia initially developed and then degenerated with the same morphological stages as normally observed. In striking contrast to the plasticity of morphology, we found that all four members of the of the fourth paralogous group of Hox genes that are expressed endogenously at the level of the graft are not upregulated in the caudad-transposed cranial mesoderm. It therefore appears that genes other than those of the Hox family normally expressed at this axial level control the position-specific morphogenesis of ectopic vertebrae formed from cranial somites. In evolutionary terms, the present results imply that occipital somites that were incorporated into the "New Head" retain the ability to develop according to their original morphogenetic fate, into vertebrae.

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Year:  1999        PMID: 10642789     DOI: 10.1006/dbio.1999.9512

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  4 in total

1.  Ectodermal Wnt6 is an early negative regulator of limb chondrogenesis in the chicken embryo.

Authors:  Poongodi Geetha-Loganathan; Suresh Nimmagadda; Bodo Christ; Ruijin Huang; Martin Scaal
Journal:  BMC Dev Biol       Date:  2010-03-25       Impact factor: 1.978

2.  Defects in sensory axon growth precede neuronal death in Brn3a-deficient mice.

Authors:  S R Eng; K Gratwick; J M Rhee; N Fedtsova; L Gan; E E Turner
Journal:  J Neurosci       Date:  2001-01-15       Impact factor: 6.167

3.  Commitment of chondrogenic precursors of the avian scapula takes place after epithelial-mesenchymal transition of the dermomyotome.

Authors:  Baigang Wang; Qin Pu; Raja De; Ketan Patel; Bodo Christ; Jörg Wilting; Ruijin Huang
Journal:  BMC Dev Biol       Date:  2010-08-31       Impact factor: 1.978

4.  Evolution of the head-trunk interface in tetrapod vertebrates.

Authors:  Elizabeth M Sefton; Bhart-Anjan S Bhullar; Zahra Mohaddes; James Hanken
Journal:  Elife       Date:  2016-04-19       Impact factor: 8.140

  4 in total

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