During the past year, the characterization of mechanisms and factors c
apable of disrupting nucleosomes during transcriptional activation has
been a recurrent theme in studies which address the contribution of n
ucleosome structure to gene regulation. In vivo studies using yeast an
d Drosophila together with biochemical purification schemes using nucl
eosome perturbation assays have provided evidence for the existence of
multiprotein complexes that are able to alleviate nucleosome repressi
on. At the same time, new insights into the mechanism of heterochromat
in formation have been gained, which have direct links to nucleosome s
tructure.