THE BARE LYMPHOCYTE SYNDROME AND THE REGULATION OF MHC EXPRESSION
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 + T cells, it is not surprising that the immune syst...
Saved in:
Published in | Annual review of immunology Vol. 19; no. 1; pp. 331 - 373 |
---|---|
Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Palo Alto, CA 94303-0139
Annual Reviews
01.01.2001
4139 El Camino Way, P.O. Box 10139 Annual Reviews, Inc USA |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | 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
+
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. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 ObjectType-Review-3 content type line 23 ObjectType-Feature-3 ObjectType-Review-1 |
ISSN: | 0732-0582 1545-3278 |
DOI: | 10.1146/annurev.immunol.19.1.331 |