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An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis

BACKGROUND: Programmed cell death is critical not only in adult tissue homeostasis but for embryogenesis as well. One of the earliest steps in development, formation of the proamniotic cavity, involves coordinated apoptosis of embryonic cells. Recent work from our group demonstrated that c-Src prote...

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Autores principales: O'Reilly, Linda P., Watkins, Simon C., Smithgall, Thomas E.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040764/
https://www.ncbi.nlm.nih.gov/pubmed/21359199
http://dx.doi.org/10.1371/journal.pone.0017157
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author O'Reilly, Linda P.
Watkins, Simon C.
Smithgall, Thomas E.
author_facet O'Reilly, Linda P.
Watkins, Simon C.
Smithgall, Thomas E.
author_sort O'Reilly, Linda P.
collection PubMed
description BACKGROUND: Programmed cell death is critical not only in adult tissue homeostasis but for embryogenesis as well. One of the earliest steps in development, formation of the proamniotic cavity, involves coordinated apoptosis of embryonic cells. Recent work from our group demonstrated that c-Src protein-tyrosine kinase activity triggers differentiation of mouse embryonic stem (mES) cells to primitive ectoderm-like cells. In this report, we identified Timeless (Tim), the mammalian ortholog of a Drosophila circadian rhythm protein, as a binding partner and substrate for c-Src and probed its role in the differentiation of mES cells. METHODOLOGY/PRINCIPAL FINDINGS: To determine whether Tim is involved in ES cell differentiation, Tim protein levels were stably suppressed using shRNA. Tim-defective ES cell lines were then tested for embryoid body (EB) formation, which models early mammalian development. Remarkably, confocal microscopy revealed that EBs formed from the Tim-knockdown ES cells failed to cavitate. Cells retained within the centers of the failed cavities strongly expressed the pluripotency marker Oct4, suggesting that further development is arrested without Tim. Immunoblots revealed reduced basal Caspase activity in the Tim-defective EBs compared to wild-type controls. Furthermore, EBs formed from Tim-knockdown cells demonstrated resistance to staurosporine-induced apoptosis, consistent with a link between Tim and programmed cell death during cavitation. CONCLUSIONS/SIGNIFICANCE: Our data demonstrate a novel function for the clock protein Tim during a key stage of early development. Specifically, EBs formed from ES cells lacking Tim showed reduced caspase activity and failed to cavitate. As a consequence, further development was halted, and the cells present in the failed cavity remained pluripotent. These findings reveal a new function for Tim in the coordination of ES cell differentiation, and raise the intriguing possibility that circadian rhythms and early development may be intimately linked.
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spelling pubmed-30407642011-02-25 An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis O'Reilly, Linda P. Watkins, Simon C. Smithgall, Thomas E. PLoS One Research Article BACKGROUND: Programmed cell death is critical not only in adult tissue homeostasis but for embryogenesis as well. One of the earliest steps in development, formation of the proamniotic cavity, involves coordinated apoptosis of embryonic cells. Recent work from our group demonstrated that c-Src protein-tyrosine kinase activity triggers differentiation of mouse embryonic stem (mES) cells to primitive ectoderm-like cells. In this report, we identified Timeless (Tim), the mammalian ortholog of a Drosophila circadian rhythm protein, as a binding partner and substrate for c-Src and probed its role in the differentiation of mES cells. METHODOLOGY/PRINCIPAL FINDINGS: To determine whether Tim is involved in ES cell differentiation, Tim protein levels were stably suppressed using shRNA. Tim-defective ES cell lines were then tested for embryoid body (EB) formation, which models early mammalian development. Remarkably, confocal microscopy revealed that EBs formed from the Tim-knockdown ES cells failed to cavitate. Cells retained within the centers of the failed cavities strongly expressed the pluripotency marker Oct4, suggesting that further development is arrested without Tim. Immunoblots revealed reduced basal Caspase activity in the Tim-defective EBs compared to wild-type controls. Furthermore, EBs formed from Tim-knockdown cells demonstrated resistance to staurosporine-induced apoptosis, consistent with a link between Tim and programmed cell death during cavitation. CONCLUSIONS/SIGNIFICANCE: Our data demonstrate a novel function for the clock protein Tim during a key stage of early development. Specifically, EBs formed from ES cells lacking Tim showed reduced caspase activity and failed to cavitate. As a consequence, further development was halted, and the cells present in the failed cavity remained pluripotent. These findings reveal a new function for Tim in the coordination of ES cell differentiation, and raise the intriguing possibility that circadian rhythms and early development may be intimately linked. Public Library of Science 2011-02-17 /pmc/articles/PMC3040764/ /pubmed/21359199 http://dx.doi.org/10.1371/journal.pone.0017157 Text en O'Reilly 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
O'Reilly, Linda P.
Watkins, Simon C.
Smithgall, Thomas E.
An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis
title An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis
title_full An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis
title_fullStr An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis
title_full_unstemmed An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis
title_short An Unexpected Role for the Clock Protein Timeless in Developmental Apoptosis
title_sort unexpected role for the clock protein timeless in developmental apoptosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3040764/
https://www.ncbi.nlm.nih.gov/pubmed/21359199
http://dx.doi.org/10.1371/journal.pone.0017157
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