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Molecular and Cellular Biology, December 2000, p. 8933-8943, Vol. 20, No. 23
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Functional Interaction between Nucleosome Assembly
Proteins and p300/CREB-Binding Protein Family Coactivators
Noriko
Shikama,
Ho Man
Chan,
Marija
Krstic-Demonacos,
Linda
Smith,
Chang-Woo
Lee,
William
Cairns, and
Nicholas B.
La Thangue*
Division of Biochemistry and Molecular
Biology, University of Glasgow, Glasgow G12 8QQ, United
Kingdom
Received 13 June 2000/Returned for modification 15 July
2000/Accepted 5 September 2000
The p300/CREB-binding protein (CBP) family of proteins consists of
coactivators that influence the activity of a wide variety of
transcription factors. Although the mechanisms that allow p300/CBP proteins to achieve transcriptional control are not clear, it is
believed that the regulation of chromatin is an important aspect of the
process. Here, we describe a new level of p300-dependent control
mediated through the functional interaction between p300/CBP and
members of the family of nucleosome assembly proteins (NAP), which
includes NAP1, NAP2, and TAF1. We find that NAP proteins, which have
previously been implicated in the regulation of transcription factor
binding to chromatin, augment the activity of different p300 targets,
including p53 and E2F, through a process that is likely to involve the
physical interaction between p300 and NAP. NAP proteins can form
oligomers, and the results show that NAP proteins can bind to both core
histones and p300 coactivator proteins, perhaps in a multicomponent
ternary complex. We also provide data in support of the idea that
histones can influence the interaction between p300 and NAP protein.
These results argue that NAP is a functionally important component of
the p300 coactivator complex and suggest that NAP may serve as a point
of integration between transcriptional coactivators and chromatin.
*
Corresponding author. Mailing address: Division of
Biochemistry and Molecular Biology, Davidson Building, University of
Glasgow, Glasgow G12 8QQ, United Kingdom. Phone: 44 141 330 5514. Fax: 44 141 330 5859. E-mail: nlathangue{at}bio.gla.ac.uk.
Molecular and Cellular Biology, December 2000, p. 8933-8943, Vol. 20, No. 23
0270-7306/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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