Histone deacetylase 1 can repress transcription by binding to Sp1.

Abstract:

:The members of the Sp1 transcription factor family can act as both negative and positive regulators of gene expression. Here we show that Sp1 can be a target for histone deacetylase 1 (HDAC1)-mediated transcriptional repression. The histone deacetylase inhibitor trichostatin A activates the chromosomally integrated murine thymidine kinase promoter in an Sp1-dependent manner. Coimmunoprecipitation experiments with Swiss 3T3 fibroblasts and 293 cells demonstrate that Sp1 and HDAC1 can be part of the same complex. The interaction between Sp1 and HDAC1 is direct and requires the carboxy-terminal domain of Sp1. Previously we have shown that the C terminus of Sp1 is necessary for the interaction with the transcription factor E2F1 (J. Karlseder, H. Rotheneder, and E. Wintersberger, Mol. Cell. Biol. 16:1659-1667, 1996). Coexpression of E2F1 interferes with HDAC1 binding to Sp1 and abolishes Sp1-mediated transcriptional repression. Our results indicate that one component of Sp1-dependent gene regulation involves competition between the transcriptional repressor HDAC1 and the transactivating factor E2F1.

journal_name

Mol Cell Biol

authors

Doetzlhofer A,Rotheneder H,Lagger G,Koranda M,Kurtev V,Brosch G,Wintersberger E,Seiser C

doi

10.1128/mcb.19.8.5504

subject

Has Abstract

pub_date

1999-08-01 00:00:00

pages

5504-11

issue

8

eissn

0270-7306

issn

1098-5549

journal_volume

19

pub_type

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