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Retroelements in the human MHC class II region
G Andersson1, A C Svensson, N Setterblad
1Department of Cell Research, Uppsala Genetic Center, Swedish University of Agricultural Sciences, Sweden. goran.andersson@cellfo.slu.se
Trends in Genetics : TIG
|April 16, 1998
Summary
Retroelements, including human endogenous retroviruses (HERVs), are abundant in the human major histocompatibility complex (MHC). These elements may play a role in autoimmune diseases linked to MHC class II genes.
Area of Science:
- Genetics
- Immunology
- Evolutionary Biology
Background:
- The human major histocompatibility complex (MHC) contains over 200 genes and dense clusters of retroelements like SINEs, LINEs, and human endogenous retroviruses (HERVs).
- Retroelements significantly influence genome plasticity and are valuable tools in evolutionary studies of the MHC.
- Human endogenous retroviruses (HERVs) are increasingly implicated in autoimmune diseases.
Purpose of the Study:
- To investigate the role of retroelements, particularly HERVs, within the MHC.
- To explore the correlation between HERV-encoded antigens, MHC class II genes, and autoimmune disease development.
- To highlight the significance of retroelements in understanding autoimmune pathogenesis.
Main Methods:
- Molecular genetic studies of the human MHC.
- Comparative analyses of retroelements within the MHC.
- Genetic analyses of autoimmune diseases and their association with MHC genes.
Main Results:
- Retroelements, including HERVs, are prevalent in the MHC and impact its genome plasticity.
- HERV-encoded superantigens are potential autoimmune genes for type I diabetes and multiple sclerosis.
- Strong associations exist between autoimmune diseases and MHC class II genes.
Conclusions:
- The presence and activity of retroelements in the MHC, especially HERVs in the MHC class II region, warrant further investigation.
- Understanding the interplay between retroviral antigens, MHC class II, and autoimmunity is crucial for future research.
- Retroelements represent a significant factor in the etiology and progression of autoimmune diseases.