A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus
Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse clinical manifestations characterized by the development of pathogenic autoantibodies manifesting in inflammation of target organs such as the kidneys, skin and joints. Genome-wide association studies have identified genetic va...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2012
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/24136
- Acceso en línea:
- https://doi.org/10.1038/gene.2012.6
https://repository.urosario.edu.co/handle/10336/24136
- Palabra clave:
- Messenger RNA
UBE2L3 protein
Ubiquitin
Ubiquitin conjugating enzyme
Unclassified drug
Article
Autoimmunity
Female
Gene expression
Genetic analysis
Genetic association
Haplotype
Human
Major clinical study
Male
Priority journal
Risk assessment
Systemic lupus erythematosus
African Americans
Alleles
Asian Continental Ancestry Group
European Continental Ancestry Group
Female
Genetic Predisposition to Disease
Haplotypes
Hispanic Americans
Humans
Linkage Disequilibrium
Male
Ubiquitin-Conjugating Enzymes
Multi-ethnic association study
Systemic lupus erythematosus
UBCH7 expression
UBE2L3
Single Nucleotide
Systemic
Lupus Erythematosus
Polymorphism
- Rights
- License
- Abierto (Texto Completo)
Summary: | Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse clinical manifestations characterized by the development of pathogenic autoantibodies manifesting in inflammation of target organs such as the kidneys, skin and joints. Genome-wide association studies have identified genetic variants in the UBE2L3 region that are associated with SLE in subjects of European and Asian ancestry. UBE2L3 encodes an ubiquitin-conjugating enzyme, UBCH7, involved in cell proliferation and immune function. In this study, we sought to further characterize the genetic association in the region of UBE2L3 and use molecular methods to determine the functional effect of the risk haplotype. We identified significant associations between variants in the region of UBE2L3 and SLE in individuals of European and Asian ancestry that exceeded a Bonferroni-corrected threshold (P and lt;1 × 10-4). A single risk haplotype was observed in all associated populations. Individuals harboring the risk haplotype display a significant increase in both UBE2L3 mRNA expression (P=0.0004) and UBCH7 protein expression (P=0.0068). The results suggest that variants carried on the SLE-associated UBE2L3 risk haplotype influence autoimmunity by modulating UBCH7 expression. © 2012 Macmillan Publishers Limited All rights reserved. |
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