The last two decades have witnessed a tremendous expansion in our knowledge
of the mechanisms employed by eukaryotic cells to control gene activity. A
critical insight to transcriptional control mechanisms was provided by the
discovery of coactivators, a diverse array of cellular factors that connec
t sequence-specific DNA binding activators to the general transcriptional m
achinery, or that help activators and the transcriptional apparatus to navi
gate through the constraints of chromatin. A number of coactivators have be
en isolated as large multifunctional complexes, and biochemical, genetic, m
olecular, and cellular strategies have all contributed to uncovering many o
f their components, activities, and modes of action. Coactivator functions
can be broadly divided into two classes: (a) adaptors that direct activator
recruitment of the transcriptional apparatus, (b) chromatin-remodeling or
-modifying enzymes. Strikingly, several distinct coactivator complexes none
theless share many subunits and appear to be assembled in a modular fashion
. Such structural and functional modularity could provide the cell with bui
lding blocks from which to construct a versatile array of coactivator compl
exes according to its needs. The extent of functional interplay between the
se different activities in gene-specific transcriptional regulation is only
now becoming apparent, and will remain an active area of research for year
s to come.