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The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain

Notch (N) signaling is central to the self-renewal of neural stem cells (NSCs) and other tissue stem cells. Its deregulation compromises tissue homeostasis and contributes to tumorigenesis and other diseases. How N regulates stem cell behavior in health and disease is not well understood. Here we sh...

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Detalles Bibliográficos
Autores principales: Wu, Yen-Chi, Lee, Kyu-Sun, Song, Yan, Gehrke, Stephan, Lu, Bingwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453605/
https://www.ncbi.nlm.nih.gov/pubmed/28520736
http://dx.doi.org/10.1371/journal.pgen.1006785
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author Wu, Yen-Chi
Lee, Kyu-Sun
Song, Yan
Gehrke, Stephan
Lu, Bingwei
author_facet Wu, Yen-Chi
Lee, Kyu-Sun
Song, Yan
Gehrke, Stephan
Lu, Bingwei
author_sort Wu, Yen-Chi
collection PubMed
description Notch (N) signaling is central to the self-renewal of neural stem cells (NSCs) and other tissue stem cells. Its deregulation compromises tissue homeostasis and contributes to tumorigenesis and other diseases. How N regulates stem cell behavior in health and disease is not well understood. Here we show that N regulates bantam (ban) microRNA to impact cell growth, a process key to NSC maintenance and particularly relied upon by tumor-forming cancer stem cells. Notch signaling directly regulates ban expression at the transcriptional level, and ban in turn feedback regulates N activity through negative regulation of the Notch inhibitor Numb. This feedback regulatory mechanism helps maintain the robustness of N signaling activity and NSC fate. Moreover, we show that a Numb-Myc axis mediates the effects of ban on nucleolar and cellular growth independently or downstream of N. Our results highlight intricate transcriptional as well as translational control mechanisms and feedback regulation in the N signaling network, with important implications for NSC biology and cancer biology.
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spelling pubmed-54536052017-06-09 The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain Wu, Yen-Chi Lee, Kyu-Sun Song, Yan Gehrke, Stephan Lu, Bingwei PLoS Genet Research Article Notch (N) signaling is central to the self-renewal of neural stem cells (NSCs) and other tissue stem cells. Its deregulation compromises tissue homeostasis and contributes to tumorigenesis and other diseases. How N regulates stem cell behavior in health and disease is not well understood. Here we show that N regulates bantam (ban) microRNA to impact cell growth, a process key to NSC maintenance and particularly relied upon by tumor-forming cancer stem cells. Notch signaling directly regulates ban expression at the transcriptional level, and ban in turn feedback regulates N activity through negative regulation of the Notch inhibitor Numb. This feedback regulatory mechanism helps maintain the robustness of N signaling activity and NSC fate. Moreover, we show that a Numb-Myc axis mediates the effects of ban on nucleolar and cellular growth independently or downstream of N. Our results highlight intricate transcriptional as well as translational control mechanisms and feedback regulation in the N signaling network, with important implications for NSC biology and cancer biology. Public Library of Science 2017-05-17 /pmc/articles/PMC5453605/ /pubmed/28520736 http://dx.doi.org/10.1371/journal.pgen.1006785 Text en © 2017 Wu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wu, Yen-Chi
Lee, Kyu-Sun
Song, Yan
Gehrke, Stephan
Lu, Bingwei
The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain
title The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain
title_full The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain
title_fullStr The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain
title_full_unstemmed The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain
title_short The bantam microRNA acts through Numb to exert cell growth control and feedback regulation of Notch in tumor-forming stem cells in the Drosophila brain
title_sort bantam microrna acts through numb to exert cell growth control and feedback regulation of notch in tumor-forming stem cells in the drosophila brain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453605/
https://www.ncbi.nlm.nih.gov/pubmed/28520736
http://dx.doi.org/10.1371/journal.pgen.1006785
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