It is essential to identify the exact location of the linker histone w
ithin nucleosomes, the fundamental packing units of chromatin, in orde
r to understand how condensed, transcriptionally inactive chromatin fo
rms. Here, using a site-specific protein-DNA photocrosslinking method(
1), we map the binding site and the orientation of the globular domain
of linker histone H5 on mixed-sequence chicken nucleosomes. We show,
in contrast to an earlier model(2), that the globular domain forms a b
ridge between one terminus of chromatosomal DNA and the DNA in the vic
inity of the dyad axis of symmetry of the core particle. Helix III of
the globular domain binds in the major groove of the first helical tur
n of the chromatosomal DNA, whereas the secondary DNA-binding site on
the opposite face of the globular domain of histone H5 makes contact w
ith the nucleosomal DNA dose to its midpoint. We also infer that helix
I and helix II of the globular domain of histone H5 probably face, re
spectively, the solvent and the nucleosome. This location places the b
asic carboxy-terminal region of the globular domain in a position from
which it could simultaneously bind the nucleosome-linking DNA strands
that exit and enter the nucleosome.