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daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71

Many tissue-specific stem cells maintain the ability to produce multiple cell types during long periods of non-division, or quiescence. FOXO transcription factors promote quiescence and stem cell maintenance, but the mechanisms by which FOXO proteins promote multipotency during quiescence are still...

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Autores principales: Wirick, Matthew J., Cale, Allison R., Smith, Isaac T., Alessi, Amelia F., Starostik, Margaret R., Cuko, Liberta, Lalk, Kyal, Schmidt, Mikayla N., Olson, Benjamin S., Salomon, Payton M., Santos, Alexis, Schmitter-Sánchez, Axel, Galagali, Himani, Ranke, Kevin J., Wolbert, Payton A., Knoblock, Macy L., Kim, John K., Karp, Xantha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8629381/
https://www.ncbi.nlm.nih.gov/pubmed/34780472
http://dx.doi.org/10.1371/journal.pgen.1009881
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author Wirick, Matthew J.
Cale, Allison R.
Smith, Isaac T.
Alessi, Amelia F.
Starostik, Margaret R.
Cuko, Liberta
Lalk, Kyal
Schmidt, Mikayla N.
Olson, Benjamin S.
Salomon, Payton M.
Santos, Alexis
Schmitter-Sánchez, Axel
Galagali, Himani
Ranke, Kevin J.
Wolbert, Payton A.
Knoblock, Macy L.
Kim, John K.
Karp, Xantha
author_facet Wirick, Matthew J.
Cale, Allison R.
Smith, Isaac T.
Alessi, Amelia F.
Starostik, Margaret R.
Cuko, Liberta
Lalk, Kyal
Schmidt, Mikayla N.
Olson, Benjamin S.
Salomon, Payton M.
Santos, Alexis
Schmitter-Sánchez, Axel
Galagali, Himani
Ranke, Kevin J.
Wolbert, Payton A.
Knoblock, Macy L.
Kim, John K.
Karp, Xantha
author_sort Wirick, Matthew J.
collection PubMed
description Many tissue-specific stem cells maintain the ability to produce multiple cell types during long periods of non-division, or quiescence. FOXO transcription factors promote quiescence and stem cell maintenance, but the mechanisms by which FOXO proteins promote multipotency during quiescence are still emerging. The single FOXO ortholog in C. elegans, daf-16, promotes entry into a quiescent and stress-resistant larval stage called dauer in response to adverse environmental cues. During dauer, stem and progenitor cells maintain or re-establish multipotency to allow normal development to resume after dauer. We find that during dauer, daf-16/FOXO prevents epidermal stem cells (seam cells) from prematurely adopting differentiated, adult characteristics. In particular, dauer larvae that lack daf-16 misexpress collagens that are normally adult-enriched. Using col-19p::gfp as an adult cell fate marker, we find that all major daf-16 isoforms contribute to opposing col-19p::gfp expression during dauer. By contrast, daf-16(0) larvae that undergo non-dauer development do not misexpress col-19p::gfp. Adult cell fate and the timing of col-19p::gfp expression are regulated by the heterochronic gene network, including lin-41 and lin-29. lin-41 encodes an RNA-binding protein orthologous to LIN41/TRIM71 in mammals, and lin-29 encodes a conserved zinc finger transcription factor. In non-dauer development, lin-41 opposes adult cell fate by inhibiting the translation of lin-29, which directly activates col-19 transcription and promotes adult cell fate. We find that during dauer, lin-41 blocks col-19p::gfp expression, but surprisingly, lin-29 is not required in this context. Additionally, daf-16 promotes the expression of lin-41 in dauer larvae. The col-19p::gfp misexpression phenotype observed in dauer larvae with reduced daf-16 requires the downregulation of lin-41, but does not require lin-29. Taken together, this work demonstrates a novel role for daf-16/FOXO as a heterochronic gene that promotes expression of lin-41/TRIM71 to contribute to multipotent cell fate in a quiescent stem cell model.
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spelling pubmed-86293812021-11-30 daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71 Wirick, Matthew J. Cale, Allison R. Smith, Isaac T. Alessi, Amelia F. Starostik, Margaret R. Cuko, Liberta Lalk, Kyal Schmidt, Mikayla N. Olson, Benjamin S. Salomon, Payton M. Santos, Alexis Schmitter-Sánchez, Axel Galagali, Himani Ranke, Kevin J. Wolbert, Payton A. Knoblock, Macy L. Kim, John K. Karp, Xantha PLoS Genet Research Article Many tissue-specific stem cells maintain the ability to produce multiple cell types during long periods of non-division, or quiescence. FOXO transcription factors promote quiescence and stem cell maintenance, but the mechanisms by which FOXO proteins promote multipotency during quiescence are still emerging. The single FOXO ortholog in C. elegans, daf-16, promotes entry into a quiescent and stress-resistant larval stage called dauer in response to adverse environmental cues. During dauer, stem and progenitor cells maintain or re-establish multipotency to allow normal development to resume after dauer. We find that during dauer, daf-16/FOXO prevents epidermal stem cells (seam cells) from prematurely adopting differentiated, adult characteristics. In particular, dauer larvae that lack daf-16 misexpress collagens that are normally adult-enriched. Using col-19p::gfp as an adult cell fate marker, we find that all major daf-16 isoforms contribute to opposing col-19p::gfp expression during dauer. By contrast, daf-16(0) larvae that undergo non-dauer development do not misexpress col-19p::gfp. Adult cell fate and the timing of col-19p::gfp expression are regulated by the heterochronic gene network, including lin-41 and lin-29. lin-41 encodes an RNA-binding protein orthologous to LIN41/TRIM71 in mammals, and lin-29 encodes a conserved zinc finger transcription factor. In non-dauer development, lin-41 opposes adult cell fate by inhibiting the translation of lin-29, which directly activates col-19 transcription and promotes adult cell fate. We find that during dauer, lin-41 blocks col-19p::gfp expression, but surprisingly, lin-29 is not required in this context. Additionally, daf-16 promotes the expression of lin-41 in dauer larvae. The col-19p::gfp misexpression phenotype observed in dauer larvae with reduced daf-16 requires the downregulation of lin-41, but does not require lin-29. Taken together, this work demonstrates a novel role for daf-16/FOXO as a heterochronic gene that promotes expression of lin-41/TRIM71 to contribute to multipotent cell fate in a quiescent stem cell model. Public Library of Science 2021-11-15 /pmc/articles/PMC8629381/ /pubmed/34780472 http://dx.doi.org/10.1371/journal.pgen.1009881 Text en © 2021 Wirick et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Wirick, Matthew J.
Cale, Allison R.
Smith, Isaac T.
Alessi, Amelia F.
Starostik, Margaret R.
Cuko, Liberta
Lalk, Kyal
Schmidt, Mikayla N.
Olson, Benjamin S.
Salomon, Payton M.
Santos, Alexis
Schmitter-Sánchez, Axel
Galagali, Himani
Ranke, Kevin J.
Wolbert, Payton A.
Knoblock, Macy L.
Kim, John K.
Karp, Xantha
daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71
title daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71
title_full daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71
title_fullStr daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71
title_full_unstemmed daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71
title_short daf-16/FOXO blocks adult cell fate in Caenorhabditis elegans dauer larvae via lin-41/TRIM71
title_sort daf-16/foxo blocks adult cell fate in caenorhabditis elegans dauer larvae via lin-41/trim71
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8629381/
https://www.ncbi.nlm.nih.gov/pubmed/34780472
http://dx.doi.org/10.1371/journal.pgen.1009881
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