Literature DB >> 22753107

The gross anatomy of the original and regenerated tail in the green anole (Anolis carolinensis).

Terrence B Ritzman1, Laura K Stroik, Emily Julik, Elizabeth D Hutchins, Eris Lasku, Dale F Denardo, Jeanne Wilson-Rawls, J Alan Rawls, Kenro Kusumi, Rebecca E Fisher.   

Abstract

This study investigates the gross anatomy of the original and the regenerated tail in the green anole (Anolis carolinensis). Dissections were conducted on 24 original and 13 regenerated tails. While the extrinsic muscles of the original tail in A. carolinensis are similar to those in other known Anolis lizard species, the extent of the origins of m. caudofemoralis longus and m. caudofemoralis brevis is more restricted. These differences may underlie variation in locomotor performance among anole ecomorphs. The intrinsic muscles of the original tail are also described, confirming previous findings and documenting new details, including muscle origins and insertions and the range of intraspecific variation. A comparison of the intrinsic muscles of the original tail and the regenerated tail muscles reveals key differences, such as the lack of interdigitating muscle segments and intramuscular septa in the regenerated tail. These findings, along with the replacement of interlocking vertebrae with a stiff, cartilaginous rod, suggest that important functional differences exist between the original and regenerated tail. In particular, the regenerated tail is predicted to be less capable of coordinated, fine movements. Studies of the physical properties and range of motion of the original and regenerated tail are required to test this hypothesis. This atlas of tail anatomy in A. carolinensis represents a key resource for developmental and genetic studies of tail regeneration in lizards, as well as studies of anole evolution and biomechanics.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22753107     DOI: 10.1002/ar.22524

Source DB:  PubMed          Journal:  Anat Rec (Hoboken)        ISSN: 1932-8486            Impact factor:   2.064


  13 in total

1.  Differences in neural stem cell identity and differentiation capacity drive divergent regenerative outcomes in lizards and salamanders.

Authors:  Aaron X Sun; Ricardo Londono; Megan L Hudnall; Rocky S Tuan; Thomas P Lozito
Journal:  Proc Natl Acad Sci U S A       Date:  2018-08-13       Impact factor: 11.205

2.  Cardiovascular biology: Switched at birth.

Authors:  Katherine E Yutzey
Journal:  Nature       Date:  2014-05-29       Impact factor: 49.962

3.  Identification of satellite cells from anole lizard skeletal muscle and demonstration of expanded musculoskeletal potential.

Authors:  Joanna Palade; Djordje Djordjevic; Elizabeth D Hutchins; Rajani M George; John A Cornelius; Alan Rawls; Joshua W K Ho; Kenro Kusumi; Jeanne Wilson-Rawls
Journal:  Dev Biol       Date:  2017-12-25       Impact factor: 3.582

4.  Developmental and adult-specific processes contribute to de novo neuromuscular regeneration in the lizard tail.

Authors:  Minami A Tokuyama; Cindy Xu; Rebecca E Fisher; Jeanne Wilson-Rawls; Kenro Kusumi; Jason M Newbern
Journal:  Dev Biol       Date:  2017-12-25       Impact factor: 3.582

Review 5.  Studying mechanisms of regeneration in amphibian and reptilian vertebrate models.

Authors:  Kenro Kusumi; Rebecca E Fisher
Journal:  Anat Rec (Hoboken)       Date:  2012-08-29       Impact factor: 2.064

6.  Transcriptomic analysis of tail regeneration in the lizard Anolis carolinensis reveals activation of conserved vertebrate developmental and repair mechanisms.

Authors:  Elizabeth D Hutchins; Glenn J Markov; Walter L Eckalbar; Rajani M George; Jesse M King; Minami A Tokuyama; Lauren A Geiger; Nataliya Emmert; Michael J Ammar; April N Allen; Ashley L Siniard; Jason J Corneveaux; Rebecca E Fisher; Juli Wade; Dale F DeNardo; J Alan Rawls; Matthew J Huentelman; Jeanne Wilson-Rawls; Kenro Kusumi
Journal:  PLoS One       Date:  2014-08-20       Impact factor: 3.240

7.  Differential expression of conserved and novel microRNAs during tail regeneration in the lizard Anolis carolinensis.

Authors:  Elizabeth D Hutchins; Walter L Eckalbar; Justin M Wolter; Marco Mangone; Kenro Kusumi
Journal:  BMC Genomics       Date:  2016-05-05       Impact factor: 3.969

8.  Expression and role of HIF-1α and HIF-2α in tissue regeneration: a study of hypoxia in house gecko tail regeneration.

Authors:  Titta Novianti; Vetnizah Juniantito; Ahmad Aulia Jusuf; Evy Ayu Arida; Sri Widia A Jusman; Mohamad Sadikin
Journal:  Organogenesis       Date:  2019-08-13       Impact factor: 2.500

9.  Genome reannotation of the lizard Anolis carolinensis based on 14 adult and embryonic deep transcriptomes.

Authors:  Walter L Eckalbar; Elizabeth D Hutchins; Glenn J Markov; April N Allen; Jason J Corneveaux; Kerstin Lindblad-Toh; Federica Di Palma; Jessica Alföldi; Matthew J Huentelman; Kenro Kusumi
Journal:  BMC Genomics       Date:  2013-01-23       Impact factor: 3.969

10.  High expressions of the cytoglobin and PGC-1α genes during the tissue regeneration of house gecko (Hemidactylus platyurus) tails.

Authors:  Titta Novianti; Vetnizah Juniantito; Ahmad Aulia Jusuf; Evy Ayu Arida; Mohamad Sadikin; Sri Widia A Jusman
Journal:  BMC Dev Biol       Date:  2020-05-11       Impact factor: 1.978

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