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The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells

The long non-coding RNA (lncRNA) Maternally Expressed Gene 3 (Meg3) is encoded within the imprinted Dlk1-Meg3 gene locus and is only maternally expressed. Meg3 has been shown to play an important role in the regulation of cellular proliferation and functions as a tumor suppressor in numerous tissues...

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Autores principales: Sommerkamp, Pia, Renders, Simon, Ladel, Luisa, Hotz-Wagenblatt, Agnes, Schönberger, Katharina, Zeisberger, Petra, Przybylla, Adriana, Sohn, Markus, Zhou, Yunli, Klibanski, Anne, Cabezas-Wallscheid, Nina, Trumpp, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375991/
https://www.ncbi.nlm.nih.gov/pubmed/30765776
http://dx.doi.org/10.1038/s41598-019-38605-8
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author Sommerkamp, Pia
Renders, Simon
Ladel, Luisa
Hotz-Wagenblatt, Agnes
Schönberger, Katharina
Zeisberger, Petra
Przybylla, Adriana
Sohn, Markus
Zhou, Yunli
Klibanski, Anne
Cabezas-Wallscheid, Nina
Trumpp, Andreas
author_facet Sommerkamp, Pia
Renders, Simon
Ladel, Luisa
Hotz-Wagenblatt, Agnes
Schönberger, Katharina
Zeisberger, Petra
Przybylla, Adriana
Sohn, Markus
Zhou, Yunli
Klibanski, Anne
Cabezas-Wallscheid, Nina
Trumpp, Andreas
author_sort Sommerkamp, Pia
collection PubMed
description The long non-coding RNA (lncRNA) Maternally Expressed Gene 3 (Meg3) is encoded within the imprinted Dlk1-Meg3 gene locus and is only maternally expressed. Meg3 has been shown to play an important role in the regulation of cellular proliferation and functions as a tumor suppressor in numerous tissues. Meg3 is highly expressed in mouse adult hematopoietic stem cells (HSCs) and strongly down-regulated in early progenitors. To address its functional role in HSCs, we used MxCre to conditionally delete Meg3 in the adult bone marrow of Meg3(mat-flox/pat-wt) mice. We performed extensive in vitro and in vivo analyses of mice carrying a Meg3 deficient blood system, but neither observed impaired hematopoiesis during homeostatic conditions nor upon serial transplantation. Furthermore, we analyzed VavCre Meg3(mat-flox/pat-wt) mice, in which Meg3 was deleted in the embryonic hematopoietic system and unexpectedly this did neither generate any hematopoietic defects. In response to interferon-mediated stimulation, Meg3 deficient adult HSCs responded highly similar compared to controls. Taken together, we report the finding, that the highly expressed imprinted lncRNA Meg3 is dispensable for the function of HSCs during homeostasis and in response to stress mediators as well as for serial reconstitution of the blood system in vivo.
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spelling pubmed-63759912019-02-19 The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells Sommerkamp, Pia Renders, Simon Ladel, Luisa Hotz-Wagenblatt, Agnes Schönberger, Katharina Zeisberger, Petra Przybylla, Adriana Sohn, Markus Zhou, Yunli Klibanski, Anne Cabezas-Wallscheid, Nina Trumpp, Andreas Sci Rep Article The long non-coding RNA (lncRNA) Maternally Expressed Gene 3 (Meg3) is encoded within the imprinted Dlk1-Meg3 gene locus and is only maternally expressed. Meg3 has been shown to play an important role in the regulation of cellular proliferation and functions as a tumor suppressor in numerous tissues. Meg3 is highly expressed in mouse adult hematopoietic stem cells (HSCs) and strongly down-regulated in early progenitors. To address its functional role in HSCs, we used MxCre to conditionally delete Meg3 in the adult bone marrow of Meg3(mat-flox/pat-wt) mice. We performed extensive in vitro and in vivo analyses of mice carrying a Meg3 deficient blood system, but neither observed impaired hematopoiesis during homeostatic conditions nor upon serial transplantation. Furthermore, we analyzed VavCre Meg3(mat-flox/pat-wt) mice, in which Meg3 was deleted in the embryonic hematopoietic system and unexpectedly this did neither generate any hematopoietic defects. In response to interferon-mediated stimulation, Meg3 deficient adult HSCs responded highly similar compared to controls. Taken together, we report the finding, that the highly expressed imprinted lncRNA Meg3 is dispensable for the function of HSCs during homeostasis and in response to stress mediators as well as for serial reconstitution of the blood system in vivo. Nature Publishing Group UK 2019-02-14 /pmc/articles/PMC6375991/ /pubmed/30765776 http://dx.doi.org/10.1038/s41598-019-38605-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sommerkamp, Pia
Renders, Simon
Ladel, Luisa
Hotz-Wagenblatt, Agnes
Schönberger, Katharina
Zeisberger, Petra
Przybylla, Adriana
Sohn, Markus
Zhou, Yunli
Klibanski, Anne
Cabezas-Wallscheid, Nina
Trumpp, Andreas
The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells
title The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells
title_full The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells
title_fullStr The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells
title_full_unstemmed The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells
title_short The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells
title_sort long non-coding rna meg3 is dispensable for hematopoietic stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375991/
https://www.ncbi.nlm.nih.gov/pubmed/30765776
http://dx.doi.org/10.1038/s41598-019-38605-8
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