Cargando…

Developmental mechanisms underlying differential claw expression in the autopodia of geckos

BACKGROUND: The limb and autopodium are frequently employed to study pattern formation during embryonic development, providing insights into how cells give rise to complex anatomical structures. With regard to the differentiation of structures at the distal tips of digits, geckos constitute an attra...

Descripción completa

Detalles Bibliográficos
Autores principales: Khannoon, Eraqi R, Russell, Anthony P, Tucker, Abigail S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397723/
https://www.ncbi.nlm.nih.gov/pubmed/25878768
http://dx.doi.org/10.1186/s13227-015-0003-9
_version_ 1782366748838723584
author Khannoon, Eraqi R
Russell, Anthony P
Tucker, Abigail S
author_facet Khannoon, Eraqi R
Russell, Anthony P
Tucker, Abigail S
author_sort Khannoon, Eraqi R
collection PubMed
description BACKGROUND: The limb and autopodium are frequently employed to study pattern formation during embryonic development, providing insights into how cells give rise to complex anatomical structures. With regard to the differentiation of structures at the distal tips of digits, geckos constitute an attractive clade, because within their ranks they exhibit multiple independent occurrences of claw loss and reduction, these being linked to the development of adhesive pads. The developmental patterns that lead to claw loss, however, remain undescribed. Among geckos, Tarentola is a genus characterized by large claws on digits III and IV of the manus and pes, with digits I, II, and V bearing only vestigial claws, or lacking them entirely. The variable expression of claws on different digits provides the opportunity to investigate the processes leading to claw reduction and loss within a single species. RESULTS: Here, we document the embryonic developmental dynamics that lead to this intraspecifically variable pattern, focusing on the cellular processes of proliferation and cell death. We find that claws initially develop on all digits of all autopodia, but, later in development, those of digits I, II, and V regress, leading to the adult condition in which robust claws are evident only on digits III and IV. Early apoptotic activity at the digit tips, followed by apoptosis of the claw primordium, premature ossification of the terminal phalanges, and later differential proliferative activity are collectively responsible for claw regression in particular digits. CONCLUSIONS: Claw reduction and loss in Tarentola result from differential intensities of apoptosis and cellular proliferation in different digits, and these processes have already had some effect before visible signs of claw development are evident. The differential processes persist through later developmental stages. Variable expression of iteratively homologous structures between digits within autopodia makes claw reduction and loss in Tarentola an excellent vehicle for exploring the developmental mechanisms that lead to evolutionary reduction and loss of structures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13227-015-0003-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4397723
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-43977232015-04-16 Developmental mechanisms underlying differential claw expression in the autopodia of geckos Khannoon, Eraqi R Russell, Anthony P Tucker, Abigail S EvoDevo Research BACKGROUND: The limb and autopodium are frequently employed to study pattern formation during embryonic development, providing insights into how cells give rise to complex anatomical structures. With regard to the differentiation of structures at the distal tips of digits, geckos constitute an attractive clade, because within their ranks they exhibit multiple independent occurrences of claw loss and reduction, these being linked to the development of adhesive pads. The developmental patterns that lead to claw loss, however, remain undescribed. Among geckos, Tarentola is a genus characterized by large claws on digits III and IV of the manus and pes, with digits I, II, and V bearing only vestigial claws, or lacking them entirely. The variable expression of claws on different digits provides the opportunity to investigate the processes leading to claw reduction and loss within a single species. RESULTS: Here, we document the embryonic developmental dynamics that lead to this intraspecifically variable pattern, focusing on the cellular processes of proliferation and cell death. We find that claws initially develop on all digits of all autopodia, but, later in development, those of digits I, II, and V regress, leading to the adult condition in which robust claws are evident only on digits III and IV. Early apoptotic activity at the digit tips, followed by apoptosis of the claw primordium, premature ossification of the terminal phalanges, and later differential proliferative activity are collectively responsible for claw regression in particular digits. CONCLUSIONS: Claw reduction and loss in Tarentola result from differential intensities of apoptosis and cellular proliferation in different digits, and these processes have already had some effect before visible signs of claw development are evident. The differential processes persist through later developmental stages. Variable expression of iteratively homologous structures between digits within autopodia makes claw reduction and loss in Tarentola an excellent vehicle for exploring the developmental mechanisms that lead to evolutionary reduction and loss of structures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13227-015-0003-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-10 /pmc/articles/PMC4397723/ /pubmed/25878768 http://dx.doi.org/10.1186/s13227-015-0003-9 Text en © Khannoon et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Khannoon, Eraqi R
Russell, Anthony P
Tucker, Abigail S
Developmental mechanisms underlying differential claw expression in the autopodia of geckos
title Developmental mechanisms underlying differential claw expression in the autopodia of geckos
title_full Developmental mechanisms underlying differential claw expression in the autopodia of geckos
title_fullStr Developmental mechanisms underlying differential claw expression in the autopodia of geckos
title_full_unstemmed Developmental mechanisms underlying differential claw expression in the autopodia of geckos
title_short Developmental mechanisms underlying differential claw expression in the autopodia of geckos
title_sort developmental mechanisms underlying differential claw expression in the autopodia of geckos
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397723/
https://www.ncbi.nlm.nih.gov/pubmed/25878768
http://dx.doi.org/10.1186/s13227-015-0003-9
work_keys_str_mv AT khannooneraqir developmentalmechanismsunderlyingdifferentialclawexpressionintheautopodiaofgeckos
AT russellanthonyp developmentalmechanismsunderlyingdifferentialclawexpressionintheautopodiaofgeckos
AT tuckerabigails developmentalmechanismsunderlyingdifferentialclawexpressionintheautopodiaofgeckos