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Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development

Krüppel-like factor 9 (Klf9) is a ubiquitously expressed transcription factor that is a feedforward regulator of multiple stress-responsive and endocrine signaling pathways. We previously described how loss of Klf9 function affects the transcriptome of zebrafish larvae sampled at a single time point...

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Autores principales: Drepanos, Laura, Gans, Ian M., Grendler, Janelle, Guitar, Sophia, Fuqua, J. Heath, Maki, Nathaniel J., Tilden, Andrea R., Graber, Joel H., Coffman, James A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382561/
https://www.ncbi.nlm.nih.gov/pubmed/37507475
http://dx.doi.org/10.1038/s41598-023-39453-3
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author Drepanos, Laura
Gans, Ian M.
Grendler, Janelle
Guitar, Sophia
Fuqua, J. Heath
Maki, Nathaniel J.
Tilden, Andrea R.
Graber, Joel H.
Coffman, James A.
author_facet Drepanos, Laura
Gans, Ian M.
Grendler, Janelle
Guitar, Sophia
Fuqua, J. Heath
Maki, Nathaniel J.
Tilden, Andrea R.
Graber, Joel H.
Coffman, James A.
author_sort Drepanos, Laura
collection PubMed
description Krüppel-like factor 9 (Klf9) is a ubiquitously expressed transcription factor that is a feedforward regulator of multiple stress-responsive and endocrine signaling pathways. We previously described how loss of Klf9 function affects the transcriptome of zebrafish larvae sampled at a single time point 5 days post-fertilization (dpf). However, klf9 expression oscillates diurnally, and the sampled time point corresponded to its expression nadir. To determine if the transcriptomic effects of the klf9(−/−) mutation vary with time of day, we performed bulk RNA-seq on 5 dpf zebrafish embryos sampled at three timepoints encompassing the predawn peak and midmorning nadir of klf9 expression. We found that while the major effects of the klf9(−/−) mutation that we reported previously are robust to time of day, the mutation has additional effects that manifest only at the predawn time point. We used a published single-cell atlas of zebrafish development to associate the effects of the klf9(−/−) mutation with different cell types and found that the mutation increased mRNA associated with digestive organs (liver, pancreas, and intestine) and decreased mRNA associated with differentiating neurons and blood. Measurements from confocally-imaged larvae suggest that overrepresentation of liver mRNA in klf9(−/−) mutants is due to development of enlarged livers.
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spelling pubmed-103825612023-07-30 Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development Drepanos, Laura Gans, Ian M. Grendler, Janelle Guitar, Sophia Fuqua, J. Heath Maki, Nathaniel J. Tilden, Andrea R. Graber, Joel H. Coffman, James A. Sci Rep Article Krüppel-like factor 9 (Klf9) is a ubiquitously expressed transcription factor that is a feedforward regulator of multiple stress-responsive and endocrine signaling pathways. We previously described how loss of Klf9 function affects the transcriptome of zebrafish larvae sampled at a single time point 5 days post-fertilization (dpf). However, klf9 expression oscillates diurnally, and the sampled time point corresponded to its expression nadir. To determine if the transcriptomic effects of the klf9(−/−) mutation vary with time of day, we performed bulk RNA-seq on 5 dpf zebrafish embryos sampled at three timepoints encompassing the predawn peak and midmorning nadir of klf9 expression. We found that while the major effects of the klf9(−/−) mutation that we reported previously are robust to time of day, the mutation has additional effects that manifest only at the predawn time point. We used a published single-cell atlas of zebrafish development to associate the effects of the klf9(−/−) mutation with different cell types and found that the mutation increased mRNA associated with digestive organs (liver, pancreas, and intestine) and decreased mRNA associated with differentiating neurons and blood. Measurements from confocally-imaged larvae suggest that overrepresentation of liver mRNA in klf9(−/−) mutants is due to development of enlarged livers. Nature Publishing Group UK 2023-07-28 /pmc/articles/PMC10382561/ /pubmed/37507475 http://dx.doi.org/10.1038/s41598-023-39453-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Drepanos, Laura
Gans, Ian M.
Grendler, Janelle
Guitar, Sophia
Fuqua, J. Heath
Maki, Nathaniel J.
Tilden, Andrea R.
Graber, Joel H.
Coffman, James A.
Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development
title Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development
title_full Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development
title_fullStr Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development
title_full_unstemmed Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development
title_short Loss of Krüppel-like factor 9 deregulates both physiological gene expression and development
title_sort loss of krüppel-like factor 9 deregulates both physiological gene expression and development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382561/
https://www.ncbi.nlm.nih.gov/pubmed/37507475
http://dx.doi.org/10.1038/s41598-023-39453-3
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