scholarly journals Different Regulation of T-Box Genes Tbx4 and Tbx5 during Limb Development and Limb Regeneration

2002 ◽  
Vol 250 (2) ◽  
pp. 383-392 ◽  
Author(s):  
Paul Khan ◽  
Barbara Linkhart ◽  
Hans-Georg Simon
Development ◽  
2018 ◽  
Vol 145 (6) ◽  
pp. dev159830 ◽  
Author(s):  
Deepak Jain ◽  
Stephen Nemec ◽  
Maëva Luxey ◽  
Yves Gauthier ◽  
Amandine Bemmo ◽  
...  

2020 ◽  
Author(s):  
C. Aztekin ◽  
T. W. Hiscock ◽  
J. B. Gurdon ◽  
J. Jullien ◽  
J. C. Marioni ◽  
...  

AbstractAbsence of a specialised wound epidermis is hypothesised to block limb regeneration in higher vertebrates. To elucidate the cellular and molecular determinants of this tissue, we performed single-cell transcriptomics in regeneration-competent, -restricted, and -incompetent Xenopus tadpoles. We identified apical-ectodermal-ridge (AER) cells as the specialised wound epidermis, and found that their abundance on the amputation plane correlates with regeneration potential and injury-induced mesenchymal plasticity. By using ex vivo regenerating limb cultures, we demonstrate that extrinsic cues produced during limb development block AER cell formation. We identify Noggin, a morphogen expressed in cartilage/bone progenitor cells, as one of the key inhibitors of AER cell formation in regeneration-incompetent tadpoles. Extrinsic inhibitory cues can be overridden by Fgf10, which operates upstream of Noggin and blocks chondrogenesis. Together, these results indicate that manipulation of the extracellular environment and/or chondrogenesis may provide a strategy to restore regeneration potential in higher vertebrates.One Sentence SummaryExtrinsic cues associated with chondrogenic progression inhibit AER cell formation and restrict limb regeneration potential.


Development ◽  
2021 ◽  
Author(s):  
Can Aztekin ◽  
Tom W. Hiscock ◽  
John Gurdon ◽  
Jerome Jullien ◽  
John Marioni ◽  
...  

Absence of a specialized wound epidermis is hypothesized to block limb regeneration in higher vertebrates. However, the factors preventing its formation in regeneration-incompetent animals are poorly understood. To characterize the endogenous molecular and cellular regulators of specialized wound epidermis formation in Xenopus laevis tadpoles, and the loss of their regeneration-competency during development, we used single-cell transcriptomics and ex vivo regenerating limb cultures. Transcriptomic analysis revealed that the specialized wound epidermis is not a novel cell state, but a re-deployment of the apical-ectodermal-ridge (AER) program underlying limb development. Enrichment of secreted inhibitory factors, including Noggin, a morphogen expressed in developing cartilage/bone progenitor cells, are identified as key inhibitors of AER cell formation in regeneration-incompetent tadpoles. These factors can be overridden by Fgf10, which operates upstream of Noggin and blocks chondrogenesis. These results indicate that manipulation of the extracellular environment and/or chondrogenesis may provide a strategy to restore regeneration potential in higher vertebrates.


Development ◽  
1998 ◽  
Vol 125 (13) ◽  
pp. 2499-2509 ◽  
Author(s):  
J.J. Gibson-Brown ◽  
S.I. Agulnik ◽  
L.M. Silver ◽  
L. Niswander ◽  
V.E. Papaioannou

We have recently shown in mice that four members of the T-box family of transcription factors (Tbx2-Tbx5) are expressed in developing limb buds, and that expression of two of these genes, Tbx4 and Tbx5, is primarily restricted to the developing hindlimbs and forelimbs, respectively. In this report, we investigate the role of these genes in limb specification and development, using the chick as a model system. We induced the formation of ectopic limbs in the flank of chick embryos to examine the relationship between the identity of the limb-specific T-box genes being expressed and the identity of limb structures that subsequently develop. We found that, whereas bud regions expressing Tbx4 developed characteristic leg structures, regions expressing Tbx5 developed characteristic wing features. In addition, heterotopic grafts of limb mesenchyme (wing bud into leg bud, and vice versa), which are known to retain the identity of the donor tissue after transplantation, retained autonomous expression of the appropriate, limb-specific T-box gene, with no evidence of regulation by the host bud. Thus there is a direct relationship between the identity of the structures that develop in normal, ectopic and recombinant limbs, and the identity of the T-box gene(s) being expressed. To investigate the regulation of T-box gene expression during limb development, we employed several other embryological manipulations. By surgically removing the apical ectodermal ridge (AER) from either wing or leg buds, we found that, in contrast to all other genes implicated in the patterning of developing appendages, maintenance of T-box gene expression is not dependent on the continued provision of signals from the AER or the zone of polarizing activity (ZPA). By generating an ectopic ZPA, by grafting a sonic hedgehog (SHH)-expressing cell pellet under the anterior AER, we found that Tbx2 expression can lie downstream of SHH. Finally, by grafting a SHH-expressing cell pellet to the anterior margin of a bud from which the AER had been removed, we found that Tbx2 may be a direct, short-range target of SHH. Our findings suggest that these genes are intimately involved in limb development and the specification of limb identity, and a new model for the evolution of vertebrate appendages is proposed.


Development ◽  
2002 ◽  
Vol 129 (22) ◽  
pp. 5161-5170 ◽  
Author(s):  
Jennifer K. Ng ◽  
Yasuhiko Kawakami ◽  
Dirk Büscher ◽  
Ángel Raya ◽  
Tohru Itoh ◽  
...  

A major gap in our knowledge of development is how the growth and identity of tissues and organs are linked during embryogenesis. The vertebrate limb is one of the best models to study these processes. Combining mutant analyses with gain- and loss-of-function approaches in zebrafish and chick embryos, we show that Tbx5, in addition to its role governing forelimb identity,is both necessary and sufficient for limb outgrowth. We find thatTbx5 functions downstream of WNT signaling to regulateFgf10, which, in turn, maintains Tbx5 expression during limb outgrowth. Furthermore, our results indicate that Tbx5 andWnt2b function together to initiate and specify forelimb outgrowth and identity. The molecular interactions governed by members of the T-box,Wnt and Fgf gene families uncovered in this study provide a framework for understanding not only limb development, but how outgrowth and identity of other tissues and organs of the embryo may be regulated.


Author(s):  
Claudia M. Arenas Gómez ◽  
Jean P. Delgado

Salamanders are the only vertebrates that can regenerate limbs as adults. This makes them ideal models to investigate cellular and molecular mechanisms of tissue regeneration. Ambystoma mexicanum and Nothopthalmus viridescens have long served as primary salamander models of limb regeneration, and the recent sequencing of the axolotl genome now provides a blueprint to mine regeneration insights from other salamander species. In particular, there is a need to study South American plethodontid salamanders that present different patterns of limb development and regeneration. A broader sampling of species using next-generation sequencing approaches is needed to reveal shared and unique mechanisms of regeneration, and more generally, the evolutionary history of salamander limb regeneration.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Tushar K. Ghosh ◽  
José J. Aparicio-Sánchez ◽  
Sarah Buxton ◽  
J. David Brook

AbstractTBX5 is a T-box family transcription factor that regulates heart and forelimb development in vertebrates and functional deficiencies in this protein result in Holt-Oram syndrome. Recently, we have shown that acetylation of TBX5 potentiates its activity and is important for heart and limb development. Here we report that class II histone deacetylases HDAC4 and HDAC5 associate with TBX5 and repress its role in cardiac gene transcription. Both HDAC4 and HDAC5 deacetylate TBX5, which promotes its relocation to the cytoplasm and HDAC4 antagonizes the physical association and functional cooperation between TBX5 and MEF2C. We also show that protein kinase D1 (PRKD1) relieves the HDAC4/5-mediated repression of TBX5. Thus, this study reveals a novel interaction of HDAC4/5 and PRKD1 in the regulation of TBX5 transcriptional activity.


Development ◽  
1981 ◽  
Vol 65 (Supplement) ◽  
pp. 151-167
Author(s):  
M. Maden

An essential component of most theories of pattern formation in epimorphic systems is that growth and pattern formation are strictly linked. Furthermore it has been assumed that epimorphic systems display size dependence, i.e. the pattern elements are always of a fixed size. These assumptions are challenged in the work described here on amphibian limb regeneration. The sizes of elements regenerating from small and large limbs and from normal and partially denervated limbs have been measured along with a detailed study of their subsequent growth stages. It is shown that the size of elements within one group of animals is remarkably constant even though their final, adult size is very different. But between groups of animals (large versus small or normal versus partially denervated) their sizes vary considerably. Therefore this classical epimorphic system is not size dependent, calling for a revision of current theoretical concepts. The similarities between this type of behaviour and that in morphallactic systems is discussed as well as similarities with growth control in limb development.


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