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Gene expression analysis of the Xenopus laevis early limb bud proximodistal axis
BACKGROUND: Limb buds develop as bilateral outgrowths of the lateral plate mesoderm and are patterned along three axes. Current models of proximal to distal patterning of early amniote limb buds suggest that two signals, a distal organizing signal from the apical epithelial ridge (AER, Fgfs) and an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796579/ https://www.ncbi.nlm.nih.gov/pubmed/35809036 http://dx.doi.org/10.1002/dvdy.517 |
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author | Hudson, Daniel T. Bromell, Jessica S. Day, Robert C. McInnes, Tyler Ward, Joanna M. Beck, Caroline W. |
author_facet | Hudson, Daniel T. Bromell, Jessica S. Day, Robert C. McInnes, Tyler Ward, Joanna M. Beck, Caroline W. |
author_sort | Hudson, Daniel T. |
collection | PubMed |
description | BACKGROUND: Limb buds develop as bilateral outgrowths of the lateral plate mesoderm and are patterned along three axes. Current models of proximal to distal patterning of early amniote limb buds suggest that two signals, a distal organizing signal from the apical epithelial ridge (AER, Fgfs) and an opposing proximal (retinoic acid [RA]) act early on pattern this axis. RESULTS: Transcriptional analysis of stage 51 Xenopus laevis hindlimb buds sectioned along the proximal‐distal axis showed that the distal region is distinct from the rest of the limb. Expression of capn8.3, a novel calpain, was located in cells immediately flanking the AER. The Wnt antagonist Dkk1 was AER‐specific in Xenopus limbs. Two transcription factors, sall1 and zic5, were expressed in distal mesenchyme. Zic5 has no described association with limb development. We also describe expression of two proximal genes, gata5 and tnn, not previously associated with limb development. Differentially expressed genes were associated with Fgf, Wnt, and RA signaling as well as differential cell adhesion and proliferation. CONCLUSIONS: We identify new candidate genes for early proximodistal limb patterning. Our analysis of RA‐regulated genes supports a role for transient RA gradients in early limb bud in proximal‐to‐distal patterning in this anamniote model organism. |
format | Online Article Text |
id | pubmed-9796579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97965792022-12-30 Gene expression analysis of the Xenopus laevis early limb bud proximodistal axis Hudson, Daniel T. Bromell, Jessica S. Day, Robert C. McInnes, Tyler Ward, Joanna M. Beck, Caroline W. Dev Dyn Patterns & Phenotypes BACKGROUND: Limb buds develop as bilateral outgrowths of the lateral plate mesoderm and are patterned along three axes. Current models of proximal to distal patterning of early amniote limb buds suggest that two signals, a distal organizing signal from the apical epithelial ridge (AER, Fgfs) and an opposing proximal (retinoic acid [RA]) act early on pattern this axis. RESULTS: Transcriptional analysis of stage 51 Xenopus laevis hindlimb buds sectioned along the proximal‐distal axis showed that the distal region is distinct from the rest of the limb. Expression of capn8.3, a novel calpain, was located in cells immediately flanking the AER. The Wnt antagonist Dkk1 was AER‐specific in Xenopus limbs. Two transcription factors, sall1 and zic5, were expressed in distal mesenchyme. Zic5 has no described association with limb development. We also describe expression of two proximal genes, gata5 and tnn, not previously associated with limb development. Differentially expressed genes were associated with Fgf, Wnt, and RA signaling as well as differential cell adhesion and proliferation. CONCLUSIONS: We identify new candidate genes for early proximodistal limb patterning. Our analysis of RA‐regulated genes supports a role for transient RA gradients in early limb bud in proximal‐to‐distal patterning in this anamniote model organism. John Wiley & Sons, Inc. 2022-07-20 2022-11 /pmc/articles/PMC9796579/ /pubmed/35809036 http://dx.doi.org/10.1002/dvdy.517 Text en © 2022 The Authors. Developmental Dynamics published by Wiley Periodicals LLC on behalf of American Association for Anatomy. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Patterns & Phenotypes Hudson, Daniel T. Bromell, Jessica S. Day, Robert C. McInnes, Tyler Ward, Joanna M. Beck, Caroline W. Gene expression analysis of the Xenopus laevis early limb bud proximodistal axis |
title | Gene expression analysis of the
Xenopus laevis
early limb bud proximodistal axis |
title_full | Gene expression analysis of the
Xenopus laevis
early limb bud proximodistal axis |
title_fullStr | Gene expression analysis of the
Xenopus laevis
early limb bud proximodistal axis |
title_full_unstemmed | Gene expression analysis of the
Xenopus laevis
early limb bud proximodistal axis |
title_short | Gene expression analysis of the
Xenopus laevis
early limb bud proximodistal axis |
title_sort | gene expression analysis of the
xenopus laevis
early limb bud proximodistal axis |
topic | Patterns & Phenotypes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796579/ https://www.ncbi.nlm.nih.gov/pubmed/35809036 http://dx.doi.org/10.1002/dvdy.517 |
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