Literature DB >> 32933441

Salamander-like tail regeneration in the West African lungfish.

Kellen Matos Verissimo1, Louise Neiva Perez1,2, Aline Cutrim Dragalzew1, Gayani Senevirathne3, Sylvain Darnet1, Wainna Renata Barroso Mendes1, Ciro Ariel Dos Santos Neves1, Erika Monteiro Dos Santos1, Cassia Nazare de Sousa Moraes1, Ahmed Elewa4, Neil Shubin3, Nadia Belinda Fröbisch2, Josane de Freitas Sousa1, Igor Schneider1,3.   

Abstract

Salamanders, frog tadpoles and diverse lizards have the remarkable ability to regenerate tails. Palaeontological data suggest that this capacity is plesiomorphic, yet when the developmental and genetic architecture of tail regeneration arose is poorly understood. Here, we show morphological and molecular hallmarks of tetrapod tail regeneration in the West African lungfish Protopterus annectens, a living representative of the sister group of tetrapods. As in salamanders, lungfish tail regeneration occurs via the formation of a proliferative blastema and restores original structures, including muscle, skeleton and spinal cord. In contrast with lizards and similar to salamanders and frogs, lungfish regenerate spinal cord neurons and reconstitute dorsoventral patterning of the tail. Similar to salamander and frog tadpoles, Shh is required for lungfish tail regeneration. Through RNA-seq analysis of uninjured and regenerating tail blastema, we show that the genetic programme deployed during lungfish tail regeneration maintains extensive overlap with that of tetrapods, with the upregulation of genes and signalling pathways previously implicated in amphibian and lizard tail regeneration. Furthermore, the lungfish tail blastema showed marked upregulation of genes encoding post-transcriptional RNA processing components and transposon-derived genes. Our results show that the developmental processes and genetic programme of tetrapod tail regeneration were present at least near the base of the sarcopterygian clade and establish the lungfish as a valuable research system for regenerative biology.

Entities:  

Keywords:  evolution; lungfish; regeneration; tail; tetrapod

Mesh:

Year:  2020        PMID: 32933441      PMCID: PMC7542818          DOI: 10.1098/rspb.2019.2939

Source DB:  PubMed          Journal:  Proc Biol Sci        ISSN: 0962-8452            Impact factor:   5.349


  59 in total

1.  A living fossil in the genome of a living fossil: Harbinger transposons in the coelacanth genome.

Authors:  Jeramiah J Smith; Kenta Sumiyama; Chris T Amemiya
Journal:  Mol Biol Evol       Date:  2011-10-31       Impact factor: 16.240

Review 2.  Tail regeneration in the Xenopus tadpole.

Authors:  Makoto Mochii; Yuka Taniguchi; Isshin Shikata
Journal:  Dev Growth Differ       Date:  2007-02       Impact factor: 2.053

3.  Vertebrate-like regeneration in the invertebrate chordate amphioxus.

Authors:  Ildikó M L Somorjai; Rajmund L Somorjai; Jordi Garcia-Fernàndez; Hector Escrivà
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-27       Impact factor: 11.205

4.  Fibroblast growth factor-2 signaling modulates matrix reorganization and cell cycle turnover rate in the regenerating tail of Hemidactylus flaviviridis.

Authors:  Anusree Pillai; Sonam Patel; Isha Ranadive; Isha Desai; Suresh Balakrishnan
Journal:  Acta Histochem       Date:  2019-11-26       Impact factor: 2.479

5.  Cell lineage tracing during Xenopus tail regeneration.

Authors:  Cesare Gargioli; Jonathan M W Slack
Journal:  Development       Date:  2004-06       Impact factor: 6.868

6.  Characterization of TGFβ signaling during tail regeneration in the leopard Gecko (Eublepharis macularius).

Authors:  Richard W D Gilbert; Matthew K Vickaryous; Alicia M Viloria-Petit
Journal:  Dev Dyn       Date:  2013-06-05       Impact factor: 3.780

Review 7.  Mechanisms of muscle dedifferentiation during regeneration.

Authors:  Karen Echeverri; Elly M Tanaka
Journal:  Semin Cell Dev Biol       Date:  2002-10       Impact factor: 7.727

8.  Harbinger transposons and an ancient HARBI1 gene derived from a transposase.

Authors:  Vladimir V Kapitonov; Jerzy Jurka
Journal:  DNA Cell Biol       Date:  2004-05       Impact factor: 3.311

Review 9.  The regeneration blastema of lizards: an amniote model for the study of appendage replacement.

Authors:  E A B Gilbert; S L Delorme; M K Vickaryous
Journal:  Regeneration (Oxf)       Date:  2015-05-11

10.  The cellular and molecular mechanisms of tissue repair and regeneration as revealed by studies in Xenopus.

Authors:  Jingjing Li; Siwei Zhang; Enrique Amaya
Journal:  Regeneration (Oxf)       Date:  2016-10-28
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  4 in total

Review 1.  Biodiversity-based development and evolution: the emerging research systems in model and non-model organisms.

Authors:  Long Zhao; Feng Gao; Shan Gao; Yujun Liang; Hongan Long; Zhiyi Lv; Ying Su; Naihao Ye; Liusuo Zhang; Chengtian Zhao; Xiaoyu Wang; Weibo Song; Shicui Zhang; Bo Dong
Journal:  Sci China Life Sci       Date:  2021-04-22       Impact factor: 6.038

Review 2.  Future Tail Tales: A Forward-Looking, Integrative Perspective on Tail Research.

Authors:  M J Schwaner; S T Hsieh; I Braasch; S Bradley; C B Campos; C E Collins; C M Donatelli; F E Fish; O E Fitch; B E Flammang; B E Jackson; A Jusufi; P J Mekdara; A Patel; B J Swalla; M Vickaryous; C P McGowan
Journal:  Integr Comp Biol       Date:  2021-09-08       Impact factor: 3.326

Review 3.  Regeneration in Echinoderms: Molecular Advancements.

Authors:  Joshua G Medina-Feliciano; José E García-Arrarás
Journal:  Front Cell Dev Biol       Date:  2021-12-17

4.  Anatomical and histological analyses reveal that tail repair is coupled with regrowth in wild-caught, juvenile American alligators (Alligator mississippiensis).

Authors:  Cindy Xu; Joanna Palade; Rebecca E Fisher; Cameron I Smith; Andrew R Clark; Samuel Sampson; Russell Bourgeois; Alan Rawls; Ruth M Elsey; Jeanne Wilson-Rawls; Kenro Kusumi
Journal:  Sci Rep       Date:  2020-11-18       Impact factor: 4.379

  4 in total

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