Interaction of CBF alpha/AML/PEBP2 alpha transcription factors with nucleosomes containing promoter sequences requires flexibility in the translational positioning of the histone octamer and exposure of the CBF alpha site
J. Gutierrez et al., Interaction of CBF alpha/AML/PEBP2 alpha transcription factors with nucleosomes containing promoter sequences requires flexibility in the translational positioning of the histone octamer and exposure of the CBF alpha site, BIOCHEM, 39(44), 2000, pp. 13565-13574
Chromatin remodeling at eukaryotic gene promoter sequences accompanies tran
scriptional activation. Both molecular events rely on specific protein-DNA
interactions that occur within these promoter sequences. Binding of CBF alp
ha /AML/PEBP2 alpha (core binding factor alpha /acute myelogenous leukemia/
polyoma enhancer binding protein 2 alpha) proteins is a key event in both
tissue-specific and developmentally regulated osteocalcin (OC) promoter act
ivity. To address linkage between chromatin organization and transcription
factor binding, we reconstituted segments of the rat OC gene proximal promo
ter into mononucleosomes and studied binding of CBF alpha proteins. We anal
yzed binding of bacterially produced Cbf alpha 2A and Cbf alpha 2B, two spl
ice variants of the human CBF alpha2 gene, and determined the effect of het
erodimerization with the Cbf beta subunit on binding activity. Our results
indicate that binding of the truncated Cbf alpha 2A protein to naked DNA is
independent of Cbf beta whereas Cbf alpha 2A binding to nucleosomal DNA wa
s enhanced by Cbf beta. In contrast, the Cbf alpha 2B interaction with eith
er naked or nucleosomal DNA was strongly dependent on heterodimerization wi
th the Cbf beta subunit, Additionally, our results demonstrate that both Cb
f alpha 2A alone and Cbf alpha 2B complexed with Cbf beta can interact with
nucleosomal DNA only if there is a degree of flexibility in the positionin
g of the histone octamer on the DNA fragment and exposure of the CBF alpha:
site. This situation was achieved with a DNA segment of 182 bp from the ra
t OC promoter that preferentially positions mononucleosomes upstream of the
CBF alpha binding site and leaves this element partially exposed. Taken to
gether, these results suggest that nucleosomal translational positioning is
a major determinant of the binding of CBF alpha factors to nucleosomal DNA
.