Repression by nuclear receptor plays important roles in a cute promyelocyti
c leukemia and other diseases. nuclear receptor corepressor (N-CoR) and SMR
T (silencing mediator of retinoic acid and thyroid hormone receptor) are co
repressor proteins whose modular structure facilitates receptor interaction
as well as translation of repression signals involving histone deacetylati
on, alterations in chromatin structure and direct interactions with the bas
al transcription machinery. Interactions between nuclear receptors and core
pressor complexes have multiple determinants. This allows regulation, and p
otentially therapeutic manipulation, of receptor, corepressor, cell-type an
d target-gene specificity.