Epigenetic mechanisms and posttranslational modifications in systemic Lupus Erythematosus

The complex physiology of eukaryotic cells is regulated through numerous mechanisms, including epigenetic changes and posttranslational modifications. The wide-ranging diversity of these mechanisms constitutes a way of dynamic regulation of the functionality of proteins, their activity, and their su...

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Autores:
Navarro Quiroz, Elkin
Chavez-Estrada, Valeria
Macias-Ochoa, Karime
Ayala-Navarro, María Fernanda
Flores-Aguilar, Aniyensy Sarai
Morales-Navarrete, Francisco
De la Cruz Lopez, Fernando
Gomez Escorcia, Lorena
G. Musso, Carlos
Aroca Martinez, Gustavo
Gonzales Torres, Henry
Diaz Perez, Anderson
Cadena Bonfanti, Andres
Sarmiento Gutierrez, Joany
Meza, Jainy
Diaz Arroyo, Esperanza
Bello Lemus, Yesit
Ahmad, Mostapha
Navarro Quiroz, Roberto
Tipo de recurso:
Fecha de publicación:
2019
Institución:
Universidad Simón Bolívar
Repositorio:
Repositorio Digital USB
Idioma:
eng
OAI Identifier:
oai:bonga.unisimon.edu.co:20.500.12442/4335
Acceso en línea:
https://hdl.handle.net/20.500.12442/4335
Palabra clave:
Posttranslational modifications
Epigenetic mechanisms
Systemic lupus erythematosus
Ubiquitination
SUMOylation
Glycosylation
Hydroxylation
Phosphorylation
Sulfation
Acetylation
Rights
License
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Description
Summary:The complex physiology of eukaryotic cells is regulated through numerous mechanisms, including epigenetic changes and posttranslational modifications. The wide-ranging diversity of these mechanisms constitutes a way of dynamic regulation of the functionality of proteins, their activity, and their subcellular localization as well as modulation of the di erential expression of genes in response to external and internal stimuli that allow an organism to respond or adapt to accordingly. However, alterations in these mechanisms have been evidenced in several autoimmune diseases, including systemic lupus erythematosus (SLE). The present review aims to provide an approach to the current knowledge of the implications of these mechanisms in SLE pathophysiology.