30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation

Hundreds post-translational modifications (PTM) were characterized among which a large variety of glycosylations including O-GlcNAcylation. Since its discovery, O-GlcNAcylation has emerged as an unavoidable PTM widespread in the living beings including animal and plant cells, protists, bacteria and...

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المؤلفون الرئيسيون: Tarik Issad, Tony Lefebvre
التنسيق: Online
اللغة:الإنجليزية
منشور في: Frontiers Media SA 2021
الموضوعات:
الوصول للمادة أونلاين:18701
الوسوم: إضافة وسم
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author Tarik Issad
Tony Lefebvre
author_browse Tarik Issad
Tony Lefebvre
author_facet Tarik Issad
Tony Lefebvre
author_sort Tarik Issad
collection Directory of Open Access Books
description Hundreds post-translational modifications (PTM) were characterized among which a large variety of glycosylations including O-GlcNAcylation. Since its discovery, O-GlcNAcylation has emerged as an unavoidable PTM widespread in the living beings including animal and plant cells, protists, bacteria and viruses. In opposition to N- and O-glycosylations, O-GlcNAcylation only consists in the transfer of a single N-acetylglucosamine moiety through a beta-linkage onto serine and threonine residues of proteins confined within the cytosol, the nucleus and the mitochondria. The O-GlcNAc group is provided by UDP-GlcNAc, the end-product of the hexosamine biosynthetic pathway located at the crossroad of cell metabolisms making O-GlcNAcylation a PTM which level tightly reflects nutritional status; therefore regulation of cell homeostasis should be intimately correlated to lifestyle and environment. Like phosphorylation, with which it can compete, O-GlcNAcylation is reversible. This versatility is managed by OGT (O-GlcNAc transferase) that transfers the GlcNAc group and OGA (O-GlcNAcase) that removes it. Also, like its unsweetened counterpart, O-GlcNAcylation controls fundamental processes, e.g. protein fate, chromatin topology, DNA demethylation and, as recently revealed, circadian clock. Deregulation of O-GlcNAc dynamism may be involved in the emergence of cancers, neuronal and metabolic disorders such as Alzheimer's or diabetes respectively. This Research Topic in Frontiers in Endocrinology is the opportunity to celebrate the thirtieth anniversary of the discovery of "O-GlcNAc" by Gerald W. Hart.
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spelling doab-20.500.12854ir-398922022-01-31T19:57:22Z 30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation Tarik Issad Tony Lefebvre RC648-665 R5-920 nutrition Hexosamine biosynthetic pathway O GlcNAcylation OGA Inflammation Metabolism OGT Cell signaling epigenetics Cancer Hundreds post-translational modifications (PTM) were characterized among which a large variety of glycosylations including O-GlcNAcylation. Since its discovery, O-GlcNAcylation has emerged as an unavoidable PTM widespread in the living beings including animal and plant cells, protists, bacteria and viruses. In opposition to N- and O-glycosylations, O-GlcNAcylation only consists in the transfer of a single N-acetylglucosamine moiety through a beta-linkage onto serine and threonine residues of proteins confined within the cytosol, the nucleus and the mitochondria. The O-GlcNAc group is provided by UDP-GlcNAc, the end-product of the hexosamine biosynthetic pathway located at the crossroad of cell metabolisms making O-GlcNAcylation a PTM which level tightly reflects nutritional status; therefore regulation of cell homeostasis should be intimately correlated to lifestyle and environment. Like phosphorylation, with which it can compete, O-GlcNAcylation is reversible. This versatility is managed by OGT (O-GlcNAc transferase) that transfers the GlcNAc group and OGA (O-GlcNAcase) that removes it. Also, like its unsweetened counterpart, O-GlcNAcylation controls fundamental processes, e.g. protein fate, chromatin topology, DNA demethylation and, as recently revealed, circadian clock. Deregulation of O-GlcNAc dynamism may be involved in the emergence of cancers, neuronal and metabolic disorders such as Alzheimer's or diabetes respectively. This Research Topic in Frontiers in Endocrinology is the opportunity to celebrate the thirtieth anniversary of the discovery of "O-GlcNAc" by Gerald W. Hart. 2021-02-11T07:33:59Z 2021-02-11T07:33:59Z 2016-03-10 08:14:32 2015 book 18701 16648714 9782889195916 https://directory.doabooks.org/handle/20.500.12854/39892 eng Frontiers Research Topics image/jpeg Attribution 4.0 International http://www.frontiersin.org/books/30_years_old_O-GlcNAc_reaches_age_of_reason_-_Regulation_of_cell_signaling_and_metabolism_by_O-GlcN/573#nogo http://journal.frontiersin.org/researchtopic/2684/30-years-old-o-glcnac-reaches-age-of-reason---regulation-of-cell-signaling-and-metabolism-by-o-glcna Frontiers Media SA 10.3389/978-2-88919-591-6 10.3389/978-2-88919-591-6 bf5ce210-e72e-4860-ba9b-c305640ff3ae 9782889195916 113 open access
spellingShingle RC648-665
R5-920
nutrition
Hexosamine biosynthetic pathway
O GlcNAcylation
OGA
Inflammation
Metabolism
OGT
Cell signaling
epigenetics
Cancer
Tarik Issad
Tony Lefebvre
30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation
title 30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation
title_full 30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation
title_fullStr 30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation
title_full_unstemmed 30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation
title_short 30 years old: O-GlcNAc Reaches Age of Reason - Regulation of Cell Signaling and Metabolism by O-GlcNAcylation
title_sort 30 years old o glcnac reaches age of reason regulation of cell signaling and metabolism by o glcnacylation
topic RC648-665
R5-920
nutrition
Hexosamine biosynthetic pathway
O GlcNAcylation
OGA
Inflammation
Metabolism
OGT
Cell signaling
epigenetics
Cancer
topic_facet RC648-665
R5-920
nutrition
Hexosamine biosynthetic pathway
O GlcNAcylation
OGA
Inflammation
Metabolism
OGT
Cell signaling
epigenetics
Cancer
url 18701
work_keys_str_mv AT tarikissad 30yearsoldoglcnacreachesageofreasonregulationofcellsignalingandmetabolismbyoglcnacylation
AT tonylefebvre 30yearsoldoglcnacreachesageofreasonregulationofcellsignalingandmetabolismbyoglcnacylation