Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.

Hydra is a unique model for studying the mechanisms underlying stem cell biology. The activity of the three stem cell lineages structuring its body constantly replenishes mature cells lost due to normal tissue turnover. By a poorly understood mechanism, stem cells are maintained through self-renewal...

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Main Authors: Alfredo Ambrosone, Valentina Marchesano, Angela Tino, Bert Hobmayer, Claudia Tortiglione
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22292012/pdf/?tool=EBI
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spelling doaj-6d0fc4b42dc1461cba80049d356ca6dd2021-03-04T12:37:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0171e3066010.1371/journal.pone.0030660Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.Alfredo AmbrosoneValentina MarchesanoAngela TinoBert HobmayerClaudia TortiglioneHydra is a unique model for studying the mechanisms underlying stem cell biology. The activity of the three stem cell lineages structuring its body constantly replenishes mature cells lost due to normal tissue turnover. By a poorly understood mechanism, stem cells are maintained through self-renewal while concomitantly producing differentiated progeny. In vertebrates, one of many genes that participate in regulating stem cell homeostasis is the protooncogene c-myc, which has been recently identified also in Hydra, and found expressed in the interstitial stem cell lineage. In the present paper, by developing a novel strategy of RNA interference-mediated gene silencing (RNAi) based on an enhanced uptake of small interfering RNAi (siRNA), we provide molecular and biological evidence for an unexpected function of the Hydra myc gene (Hymyc1) in the homeostasis of the interstitial stem cell lineage. We found that Hymyc1 inhibition impairs the balance between stem cell self renewal/differentiation, as shown by the accumulation of stem cell intermediate and terminal differentiation products in genetically interfered animals. The identical phenotype induced by the 10058-F4 inhibitor, a disruptor of c-Myc/Max dimerization, demonstrates the specificity of the RNAi approach. We show the kinetic and the reversible feature of Hymyc1 RNAi, together with the effects displayed on regenerating animals. Our results show the involvement of Hymyc1 in the control of interstitial stem cell dynamics, provide new clues to decipher the molecular control of the cell and tissue plasticity in Hydra, and also provide further insights into the complex myc network in higher organisms. The ability of Hydra cells to uptake double stranded RNA and to trigger a RNAi response lays the foundations of a comprehensive analysis of the RNAi response in Hydra allowing us to track back in the evolution and the origin of this process.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22292012/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Alfredo Ambrosone
Valentina Marchesano
Angela Tino
Bert Hobmayer
Claudia Tortiglione
spellingShingle Alfredo Ambrosone
Valentina Marchesano
Angela Tino
Bert Hobmayer
Claudia Tortiglione
Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.
PLoS ONE
author_facet Alfredo Ambrosone
Valentina Marchesano
Angela Tino
Bert Hobmayer
Claudia Tortiglione
author_sort Alfredo Ambrosone
title Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.
title_short Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.
title_full Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.
title_fullStr Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.
title_full_unstemmed Hymyc1 downregulation promotes stem cell proliferation in Hydra vulgaris.
title_sort hymyc1 downregulation promotes stem cell proliferation in hydra vulgaris.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Hydra is a unique model for studying the mechanisms underlying stem cell biology. The activity of the three stem cell lineages structuring its body constantly replenishes mature cells lost due to normal tissue turnover. By a poorly understood mechanism, stem cells are maintained through self-renewal while concomitantly producing differentiated progeny. In vertebrates, one of many genes that participate in regulating stem cell homeostasis is the protooncogene c-myc, which has been recently identified also in Hydra, and found expressed in the interstitial stem cell lineage. In the present paper, by developing a novel strategy of RNA interference-mediated gene silencing (RNAi) based on an enhanced uptake of small interfering RNAi (siRNA), we provide molecular and biological evidence for an unexpected function of the Hydra myc gene (Hymyc1) in the homeostasis of the interstitial stem cell lineage. We found that Hymyc1 inhibition impairs the balance between stem cell self renewal/differentiation, as shown by the accumulation of stem cell intermediate and terminal differentiation products in genetically interfered animals. The identical phenotype induced by the 10058-F4 inhibitor, a disruptor of c-Myc/Max dimerization, demonstrates the specificity of the RNAi approach. We show the kinetic and the reversible feature of Hymyc1 RNAi, together with the effects displayed on regenerating animals. Our results show the involvement of Hymyc1 in the control of interstitial stem cell dynamics, provide new clues to decipher the molecular control of the cell and tissue plasticity in Hydra, and also provide further insights into the complex myc network in higher organisms. The ability of Hydra cells to uptake double stranded RNA and to trigger a RNAi response lays the foundations of a comprehensive analysis of the RNAi response in Hydra allowing us to track back in the evolution and the origin of this process.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22292012/pdf/?tool=EBI
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