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Автор Reith, Walter
Автор Mach, Bernard
Дата выпуска 2001
dc.description ▪ Abstract  The bare lymphocyte syndrome (BLS) is a hereditary immunodeficiency resulting from the absence of major istocompatibility complex class II (MHCII) expression. Considering the central role of MHCII molecules in the development and activation of CD4<sup>+</sup> T cells, it is not surprising that the immune system of the patients is severely impaired. BLS is the prototype of a “disease of gene regulation.” The affected genes encode RFXANK, RFX5, RFXAP, and CIITA, four regulatory factors that are highly specific and essential for MHCII genes. The first three are subunits of RFX, a trimeric complex that binds to all MHCII promoters. CIITA is a non-DNA-binding coactivator that functions as the master control factor for MHCII expression. The study of RFX and CIITA has made major contributions to our comprehension of the molecular mechanisms controlling MHCII genes and has made this system into a textbook model for the regulation of gene expression.
Формат application.pdf
Издатель Annual Reviews
Копирайт Annual Reviews
Название THE BARE LYMPHOCYTE SYNDROME AND THE REGULATION OF MHC EXPRESSION
DOI 10.1146/annurev.immunol.19.1.331
Print ISSN 0732-0582
Журнал Annual Review of Immunology
Том 19
Первая страница 331
Последняя страница 373
Аффилиация Reith, Walter; Jeantet Laboratory of Molecular Genetics, Department of Genetics and Microbiology, University of Geneva Medical School, 1 rue Michel-Servet, Geneva 4, 1211 Switzerland; e-mail: Walter.Reith@medecine.unige.ch Bernard.Mach@medecine.unige.ch

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