Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal Differentiation

Summary: The planarian epidermis provides an excellent model to explore adult stem cell (ASC) lineage development due to well-characterized and distinct spatiotemporal phases during lineage progression. Using flow cytometry-isolated cells enriched in epidermal progenitors, we performed transcription...

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Main Authors: Shu Jun Zhu, Bret J. Pearson
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124718314414
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spelling doaj-57b363dc51584012a791d25e2a78dd0d2020-11-25T01:46:35ZengElsevierCell Reports2211-12472018-10-012513846.e3Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal DifferentiationShu Jun Zhu0Bret J. Pearson1Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, ON M5G0A4, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, CanadaProgram in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, ON M5G0A4, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada; Ontario Institute for Cancer Research, Toronto, ON, Canada; Corresponding authorSummary: The planarian epidermis provides an excellent model to explore adult stem cell (ASC) lineage development due to well-characterized and distinct spatiotemporal phases during lineage progression. Using flow cytometry-isolated cells enriched in epidermal progenitors, we performed transcriptional profiling and RNAi screening to uncover regulators of epidermal differentiation. We identified a MYB-type transcription factor (Smed-myb-1) required for the specification of the first temporal phase of post-mitotic maturation. Knockdown of myb-1 abolished the early progenitor phase of differentiation without ceasing production of subsequent epidermal progenitor states or homeostatic turnover and regeneration of the epidermis. Further examination revealed accelerated maturation of ASC descendants, with premature entry into subsequent progeny phases and, ultimately, the epidermis. These results demonstrate that a spatiotemporal shift in lineage progression occurs in the absence of the early progenitor state after myb-1 RNAi, and identify myb-1 as a critical regulator of the early temporal window in stepwise specification during planarian epidermal differentiation. : Planarian stem cell differentiation into the epidermis is a multistep process with distinct spatiotemporal progenitor phases. Zhu and Pearson show that a putative MYB-type transcription factor facilitates correct progression through these phases, ensuring appropriate timing of maturation. Keywords: differentiation, lineage development, adult stem cells, Lophotrochozoan, planarians, Schmidtea mediterraneahttp://www.sciencedirect.com/science/article/pii/S2211124718314414
collection DOAJ
language English
format Article
sources DOAJ
author Shu Jun Zhu
Bret J. Pearson
spellingShingle Shu Jun Zhu
Bret J. Pearson
Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal Differentiation
Cell Reports
author_facet Shu Jun Zhu
Bret J. Pearson
author_sort Shu Jun Zhu
title Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal Differentiation
title_short Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal Differentiation
title_full Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal Differentiation
title_fullStr Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal Differentiation
title_full_unstemmed Smed-myb-1 Specifies Early Temporal Identity during Planarian Epidermal Differentiation
title_sort smed-myb-1 specifies early temporal identity during planarian epidermal differentiation
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2018-10-01
description Summary: The planarian epidermis provides an excellent model to explore adult stem cell (ASC) lineage development due to well-characterized and distinct spatiotemporal phases during lineage progression. Using flow cytometry-isolated cells enriched in epidermal progenitors, we performed transcriptional profiling and RNAi screening to uncover regulators of epidermal differentiation. We identified a MYB-type transcription factor (Smed-myb-1) required for the specification of the first temporal phase of post-mitotic maturation. Knockdown of myb-1 abolished the early progenitor phase of differentiation without ceasing production of subsequent epidermal progenitor states or homeostatic turnover and regeneration of the epidermis. Further examination revealed accelerated maturation of ASC descendants, with premature entry into subsequent progeny phases and, ultimately, the epidermis. These results demonstrate that a spatiotemporal shift in lineage progression occurs in the absence of the early progenitor state after myb-1 RNAi, and identify myb-1 as a critical regulator of the early temporal window in stepwise specification during planarian epidermal differentiation. : Planarian stem cell differentiation into the epidermis is a multistep process with distinct spatiotemporal progenitor phases. Zhu and Pearson show that a putative MYB-type transcription factor facilitates correct progression through these phases, ensuring appropriate timing of maturation. Keywords: differentiation, lineage development, adult stem cells, Lophotrochozoan, planarians, Schmidtea mediterranea
url http://www.sciencedirect.com/science/article/pii/S2211124718314414
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