A robust transcriptional program in newts undergoing multiple events of lens regeneration throughout their lifespan

Author:

Sousounis Konstantinos1,Qi Feng2,Yadav Manisha C3,Millán José Luis3,Toyama Fubito4,Chiba Chikafumi5,Eguchi Yukiko6,Eguchi Goro6,Tsonis Panagiotis A13

Affiliation:

1. Department of Biology, University of Dayton, Dayton, United States

2. Sanford Burnham Prebys Medical Discovery Institute at Lake Nona, Orlando, United States

3. Sanford Children's Health Research Center, Sanford-Burnham-Prebys Medical Discovery Institute, La Jolla, United States

4. Graduate School of Engineering, Utsunomiya University, Utsunomiya, Japan

5. Faculty of Life and Environmental Sciences, Tsukuba University, Tsukuba, Japan

6. National Institute for Basic Biology, National Institutes for Natural Sciences, Okazaki, Japan

Abstract

Newts have the ability to repeatedly regenerate their lens even during ageing. However, it is unclear whether this regeneration reflects an undisturbed genetic activity. To answer this question, we compared the transcriptomes of lenses, irises and tails from aged newts that had undergone lens regeneration 19 times with the equivalent tissues from young newts that had never experienced lens regeneration. Our analysis indicates that repeatedly regenerated lenses showed a robust transcriptional program comparable to young never-regenerated lenses. In contrast, the tail, which was never regenerated, showed gene expression signatures of ageing. Our analysis strongly suggests that, with respect to gene expression, the regenerated lenses have not deviated from a robust transcriptional program even after multiple events of regeneration throughout the life of the newt. In addition, our study provides a new paradigm in biology, and establishes the newt as a key model for the study of regeneration in relation to ageing.

Funder

National Eye Institute

KAKENHI

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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4. Missense mutations in MIP underlie autosomal dominant ‘polymorphic’ and lamellar cataracts linked to 12q;Berry;Nature Genetics,2000

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