miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.

Lens regeneration in adult newts occurs via transdifferentiation of the pigment epithelial cells (PECs) of the dorsal iris. The same source of cells from the ventral iris is not able to undergo this process. In an attempt to understand this restriction we have studied in the past expression patterns...

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Main Authors: Kenta Nakamura, Nobuyasu Maki, Albert Trinh, Heidi W Trask, Jiang Gui, Craig R Tomlinson, Panagiotis A Tsonis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-08-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2920319?pdf=render
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spelling doaj-f84ebe01b00f46a2a2a269c5c1726db72020-11-24T20:46:38ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-08-0158e1205810.1371/journal.pone.0012058miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.Kenta NakamuraNobuyasu MakiAlbert TrinhHeidi W TraskJiang GuiCraig R TomlinsonPanagiotis A TsonisLens regeneration in adult newts occurs via transdifferentiation of the pigment epithelial cells (PECs) of the dorsal iris. The same source of cells from the ventral iris is not able to undergo this process. In an attempt to understand this restriction we have studied in the past expression patterns of miRNAs. Among several miRNAs we have found that mir-148 shows an up-regulation in the ventral iris, while members of the let-7 family showed down-regulation in dorsal iris during dedifferentiation.We have performed gain- and loss-of-function experiments of mir-148 and let-7b in an attempt to delineate their function. We find that up-regulation of mir-148 caused significant decrease in the proliferation rates of ventral PECs only, while up-regulation of let-7b affected proliferation of both dorsal and ventral PECs. Neither miRNA was able to affect lens morphogenesis or induction. To further understand how this effect of miRNA up-regulation is mediated we examined global expression of miRNAs after up-regulation of mir148 and let-7b. Interestingly, we identified a novel level of mirRNA regulation, which might indicate that miRNAs are regulated as a network.The major conclusion is that different miRNAs can control proliferation in the dorsal or ventral iris possibly by a different mechanism. Of interest is that down-regulation of the let-7 family members has also been documented in other systems undergoing reprogramming, such as in stem cells or oocytes. This might indicate that reprogramming during newt regeneration shares common molecular signatures with reprogramming in stem or germ cells. On the other hand that miRNAs can regulate the levels of other miRNAs is a novel level of regulation, which might provide new insights on their function.http://europepmc.org/articles/PMC2920319?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kenta Nakamura
Nobuyasu Maki
Albert Trinh
Heidi W Trask
Jiang Gui
Craig R Tomlinson
Panagiotis A Tsonis
spellingShingle Kenta Nakamura
Nobuyasu Maki
Albert Trinh
Heidi W Trask
Jiang Gui
Craig R Tomlinson
Panagiotis A Tsonis
miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.
PLoS ONE
author_facet Kenta Nakamura
Nobuyasu Maki
Albert Trinh
Heidi W Trask
Jiang Gui
Craig R Tomlinson
Panagiotis A Tsonis
author_sort Kenta Nakamura
title miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.
title_short miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.
title_full miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.
title_fullStr miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.
title_full_unstemmed miRNAs in newt lens regeneration: specific control of proliferation and evidence for miRNA networking.
title_sort mirnas in newt lens regeneration: specific control of proliferation and evidence for mirna networking.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-08-01
description Lens regeneration in adult newts occurs via transdifferentiation of the pigment epithelial cells (PECs) of the dorsal iris. The same source of cells from the ventral iris is not able to undergo this process. In an attempt to understand this restriction we have studied in the past expression patterns of miRNAs. Among several miRNAs we have found that mir-148 shows an up-regulation in the ventral iris, while members of the let-7 family showed down-regulation in dorsal iris during dedifferentiation.We have performed gain- and loss-of-function experiments of mir-148 and let-7b in an attempt to delineate their function. We find that up-regulation of mir-148 caused significant decrease in the proliferation rates of ventral PECs only, while up-regulation of let-7b affected proliferation of both dorsal and ventral PECs. Neither miRNA was able to affect lens morphogenesis or induction. To further understand how this effect of miRNA up-regulation is mediated we examined global expression of miRNAs after up-regulation of mir148 and let-7b. Interestingly, we identified a novel level of mirRNA regulation, which might indicate that miRNAs are regulated as a network.The major conclusion is that different miRNAs can control proliferation in the dorsal or ventral iris possibly by a different mechanism. Of interest is that down-regulation of the let-7 family members has also been documented in other systems undergoing reprogramming, such as in stem cells or oocytes. This might indicate that reprogramming during newt regeneration shares common molecular signatures with reprogramming in stem or germ cells. On the other hand that miRNAs can regulate the levels of other miRNAs is a novel level of regulation, which might provide new insights on their function.
url http://europepmc.org/articles/PMC2920319?pdf=render
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