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O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development

BACKGROUND: The post-translational addition of the monosaccharide O-linked β-N-acetylglucosamine (O-GlcNAc) regulates the activity of a wide variety of nuclear and cytoplasmic proteins. The enzymes O-GlcNAc Transferase (Ogt) and O-GlcNAcase (Oga) catalyze, respectively, the attachment and removal of...

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Autores principales: Webster, Danielle M, Teo, Chin Fen, Sun, Yuhua, Wloga, Dorota, Gay, Steven, Klonowski, Kimberly D, Wells, Lance, Dougan, Scott T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680843/
https://www.ncbi.nlm.nih.gov/pubmed/19383152
http://dx.doi.org/10.1186/1471-213X-9-28
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author Webster, Danielle M
Teo, Chin Fen
Sun, Yuhua
Wloga, Dorota
Gay, Steven
Klonowski, Kimberly D
Wells, Lance
Dougan, Scott T
author_facet Webster, Danielle M
Teo, Chin Fen
Sun, Yuhua
Wloga, Dorota
Gay, Steven
Klonowski, Kimberly D
Wells, Lance
Dougan, Scott T
author_sort Webster, Danielle M
collection PubMed
description BACKGROUND: The post-translational addition of the monosaccharide O-linked β-N-acetylglucosamine (O-GlcNAc) regulates the activity of a wide variety of nuclear and cytoplasmic proteins. The enzymes O-GlcNAc Transferase (Ogt) and O-GlcNAcase (Oga) catalyze, respectively, the attachment and removal of O-GlcNAc to target proteins. In adult mice, Ogt and Oga attenuate the response to insulin by modifying several components of the signal transduction pathway. Complete loss of ogt function, however, is lethal to mouse embryonic stem cells, suggesting that the enzyme has additional, unstudied roles in development. We have utilized zebrafish as a model to determine role of O-GlcNAc modifications in development. Zebrafish has two ogt genes, encoding six different enzymatic isoforms that are expressed maternally and zygotically. RESULTS: We manipulated O-GlcNAc levels in zebrafish embryos by overexpressing zebrafish ogt, human oga or by injecting morpholinos against ogt transcripts. Each of these treatments results in embryos with shortened body axes and reduced brains at 24 hpf. The embryos had 23% fewer cells than controls, and displayed increased rates of cell death as early as the mid-gastrula stages. An extensive marker analysis indicates that derivatives of three germ layers are reduced to variable extents, and the embryos are severely disorganized after gastrulation. Overexpression of Ogt and Oga delayed epiboly and caused a severe disorganization of the microtubule and actin based cytoskeleton in the extra-embryonic yolk syncytial layer (YSL). The cytoskeletal defects resemble those previously reported for embryos lacking function of the Pou5f1/Oct4 transcription factor spiel ohne grenzen. Consistent with this, Pou5f1/Oct4 is modified by O-GlcNAc in human embryonic stem cells. CONCLUSION: We conclude that O-GlcNAc modifications control the activity of proteins that regulate apoptosis and epiboly movements, but do not seem to regulate germ layer specification. O-GlcNAc modifies the transcription factor Spiel ohne grenzen/Pou5f1 and may regulate its activity.
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spelling pubmed-26808432009-05-13 O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development Webster, Danielle M Teo, Chin Fen Sun, Yuhua Wloga, Dorota Gay, Steven Klonowski, Kimberly D Wells, Lance Dougan, Scott T BMC Dev Biol Research Article BACKGROUND: The post-translational addition of the monosaccharide O-linked β-N-acetylglucosamine (O-GlcNAc) regulates the activity of a wide variety of nuclear and cytoplasmic proteins. The enzymes O-GlcNAc Transferase (Ogt) and O-GlcNAcase (Oga) catalyze, respectively, the attachment and removal of O-GlcNAc to target proteins. In adult mice, Ogt and Oga attenuate the response to insulin by modifying several components of the signal transduction pathway. Complete loss of ogt function, however, is lethal to mouse embryonic stem cells, suggesting that the enzyme has additional, unstudied roles in development. We have utilized zebrafish as a model to determine role of O-GlcNAc modifications in development. Zebrafish has two ogt genes, encoding six different enzymatic isoforms that are expressed maternally and zygotically. RESULTS: We manipulated O-GlcNAc levels in zebrafish embryos by overexpressing zebrafish ogt, human oga or by injecting morpholinos against ogt transcripts. Each of these treatments results in embryos with shortened body axes and reduced brains at 24 hpf. The embryos had 23% fewer cells than controls, and displayed increased rates of cell death as early as the mid-gastrula stages. An extensive marker analysis indicates that derivatives of three germ layers are reduced to variable extents, and the embryos are severely disorganized after gastrulation. Overexpression of Ogt and Oga delayed epiboly and caused a severe disorganization of the microtubule and actin based cytoskeleton in the extra-embryonic yolk syncytial layer (YSL). The cytoskeletal defects resemble those previously reported for embryos lacking function of the Pou5f1/Oct4 transcription factor spiel ohne grenzen. Consistent with this, Pou5f1/Oct4 is modified by O-GlcNAc in human embryonic stem cells. CONCLUSION: We conclude that O-GlcNAc modifications control the activity of proteins that regulate apoptosis and epiboly movements, but do not seem to regulate germ layer specification. O-GlcNAc modifies the transcription factor Spiel ohne grenzen/Pou5f1 and may regulate its activity. BioMed Central 2009-04-21 /pmc/articles/PMC2680843/ /pubmed/19383152 http://dx.doi.org/10.1186/1471-213X-9-28 Text en Copyright © 2009 Webster et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Webster, Danielle M
Teo, Chin Fen
Sun, Yuhua
Wloga, Dorota
Gay, Steven
Klonowski, Kimberly D
Wells, Lance
Dougan, Scott T
O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development
title O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development
title_full O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development
title_fullStr O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development
title_full_unstemmed O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development
title_short O-GlcNAc modifications regulate cell survival and epiboly during zebrafish development
title_sort o-glcnac modifications regulate cell survival and epiboly during zebrafish development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680843/
https://www.ncbi.nlm.nih.gov/pubmed/19383152
http://dx.doi.org/10.1186/1471-213X-9-28
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