DNA in the nucleus of eukaryotic cells is organized in chromatin, a nucleop
rotein complex containing roughly half DNA and half protein. The nucleosome
is the underlying DNA packaging element in chromatin, repeating approximat
ely every 200 base pairs over essentially the entire genome. Our crystal st
ructure of the nucleosome core particle explains in atomic detail how DNA i
n its first level of organization is kept untangled by the histone protein
octamer and clarifies the unique role the nucleosome plays in the expressio
n of genetic information. Dynamic assembly and disassembly of the chromatin
fiber, the higher-order arrangement of nucleosomes, most probably defines
the crucial step in controlling DNA access enabling efficient regulation of
gene readout. Multiprotein complexes, here designated 'regulasomes', are b
ound at specific sites within chromatin to coalesce the histone modificatio
n and chromatin remodeling protein assemblies that affect the stability and
structure of the chromatin fiber. The formation of a particular regulasome
depends on cooperative interaction between the transcription factor protei
ns comprising it, and on their interaction with specific DNA sequences. Our
crystal structures of selected transcription factor complexes bound to the
ir target site DNA contribute to the structural basis of how specificity of
gene expression is achieved.