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APO-1/Fas gene: Structural and functional characteristics in systemic lupus erythematosus and other autoimmune diseases.
Indian J Hum Genet ; 2009 Sept; 15(3): 98-102
Article Dans Anglais | IMSEAR | ID: sea-138880
ABSTRACT
Systemic lupus erythematosus (SLE) is an autoimmune disorder affecting multiple organ systems. It is characterized by the presence of autoantibodies reactive against various self-antigens. Susceptibility to SLE is found to be associated with many major histocompatibility complex (MHC) and non-MHC genes, one of which is APO-1/Fas gene, which is present on chromosome 10 in humans. The APO-1/Fas promoter contains consensus sequences for binding of several transcription factors that affect the intensity of Fas expression in cells. The mutations in the APO-1/Fas promoter are associated with risk and severity in various autoimmune diseases and other malignancies. The APO-1/Fas receptor is expressed by many cell types. Two forms of APO-1/Fas protein that are involved in regulation of apoptosis have been identified. Fas receptor-mediated apoptosis plays a physiological and pathological role in killing of infected cell targets. In this review, we have focused on APO-1/Fas gene structure, promoter variants and its association with SLE and other autoimmune diseases. Functional aspects of Fas receptor in apoptosis are also discussed.
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Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) Sujet Principal: Maladies auto-immunes / Chromosomes humains de la paire 10 / Protéines de fusion recombinantes / Femelle / Humains / Adolescent / Apoptose / Antigènes CD95 / Adulte / Lupus érythémateux disséminé Type d'étude: Étude pronostique langue: Anglais Texte intégral: Indian J Hum Genet Année: 2009 Type: Article

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Texte intégral: Disponible Indice: IMSEAR (Asie du Sud-Est) Sujet Principal: Maladies auto-immunes / Chromosomes humains de la paire 10 / Protéines de fusion recombinantes / Femelle / Humains / Adolescent / Apoptose / Antigènes CD95 / Adulte / Lupus érythémateux disséminé Type d'étude: Étude pronostique langue: Anglais Texte intégral: Indian J Hum Genet Année: 2009 Type: Article