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Molecular and Cellular Biology, September 2005, p. 7534-7545, Vol. 25, No. 17
0270-7306/05/$08.00+0     doi:10.1128/MCB.25.17.7534-7545.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Human Histone Chaperone Nucleophosmin Enhances Acetylation-Dependent Chromatin Transcription{dagger}

V. Swaminathan, A. Hari Kishore, K. K. Febitha, and Tapas K. Kundu*

Transcription and Disease Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Center for Advanced Scientific Research, Jakkur, Bangalore 64, India

Received 1 February 2005/ Returned for modification 23 February 2005/ Accepted 23 May 2005

Histone chaperones are a group of proteins that aid in the dynamic chromatin organization during different cellular processes. Here, we report that the human histone chaperone nucleophosmin interacts with the core histones H3, H2B, and H4 but that this histone interaction is not sufficient to confer the chaperone activity. Significantly, nucleophosmin enhances the acetylation-dependent chromatin transcription and it becomes acetylated both in vitro and in vivo. Acetylation of nucleophosmin and the core histones was found to be essential for the enhancement of chromatin transcription. The acetylated NPM1 not only shows an increased affinity toward acetylated histones but also shows enhanced histone transfer ability. Presumably, nucleophosmin disrupts the nucleosomal structure in an acetylation-dependent manner, resulting in the transcriptional activation. These results establish nucleophosmin (NPM1) as a human histone chaperone that becomes acetylated, resulting in the enhancement of chromatin transcription.


* Corresponding author. Mailing address: Transcription and Disease Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Center for Advanced Scientific Research, Jakkur, Bangalore 64, India. Phone: 91-80-22082840. Fax: 91-80-22082766. E-mail: tapas{at}jncasr.ac.in.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.


Molecular and Cellular Biology, September 2005, p. 7534-7545, Vol. 25, No. 17
0022-538X/05/$08.00+0     doi:10.1128/MCB.25.17.7534-7545.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




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