The MHC class I complex, which binds and presents peptide antigen, is compo
sed of a class I heavy chain and the beta(2)-microglobulin light chain. HIV
-1, which induces a profound immunodeficiency in infected individuals, enco
des proteins that cause decreased expression of class I heavy chain. We now
report that the HIV Tat protein, which is a potent transactivator of viral
transcription, is also a potent repressor of the beta(2)-microglobulin gen
e. Repression is mediated through the basal promoter of the beta(2)-microgl
obulin gene, which is shown to be predominantly regulated by an initiator e
lement. Tat repression is further augmented by the short viral transcript,
TAR, which interacts with Tat. Tat-mediated repression of beta(2)-microglob
ulin expression, together with its known repression of class I gene transcr
iption, provides an effective mechanism by which HIV could prevent cell sur
face expression of the MHC class I complex and avoid immune surveillance. P
ublished by Elsevier Science Ltd.