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Molecular and Cellular Biology, June 2008, p. 3623-3638, Vol. 28, No. 11
0270-7306/08/$08.00+0     doi:10.1128/MCB.01152-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

RelA Ser²⁷⁶ Phosphorylation Is Required for Activation of a Subset of NF-B-Dependent Genes by Recruiting Cyclin-Dependent Kinase 9/Cyclin T1 Complexes ^,

David E. Nowak,^1, Bing Tian,^1, Mohammad Jamaluddin,¹ Istvan Boldogh,^2,4 Leoncio A. Vergara,³ Sanjeev Choudhary,¹ and Allan R. Brasier^1,4*

Departments of Medicine,¹ Microbiology and Immunology,² Neuroscience and Cell Biology,³ The Sealy Center for Molecular Medicine, The University of Texas Medical Branch, Galveston, Texas 77555-1060⁴

Received 27 June 2007/ Returned for modification 20 August 2007/ Accepted 11 March 2008

NF-B plays a central role in cytokine-inducible inflammatory gene expression. Previously we empirically determined the identity of 92 members of the genetic network under direct NF-B/RelA control that show marked heterogeneity in magnitude of transcriptional induction and kinetics of peak activation. To investigate this network further, we have applied a recently developed two-step chromatin immunoprecipitation assay that accurately reflects association and disassociation of RelA binding to its chromatin targets. Although inducible RelA binding occurs with similar kinetics on all NF-B-dependent genes, serine 276 (Ser²⁷⁶)-phosphorylated RelA binding is seen primarily on a subset of genes that are rapidly induced by tumor necrosis factor (TNF), including Gro-β, interleukin-8 (IL-8), and IB. Previous work has shown that TNF-inducible RelA Ser²⁷⁶ phosphorylation is controlled by a reactive oxygen species (ROS)-protein kinase A signaling pathway. To further understand the role of phospho-Ser²⁷⁶ RelA in target gene expression, we inhibited its formation by ROS scavengers and antioxidants, treatments that disrupt phospho-Ser²⁷⁶ formation but not the translocation and DNA binding of nonphosphorylated RelA. Here we find that phospho-Ser²⁷⁶ RelA is required only for activation of IL-8 and Gro-β, with IB being unaffected. These data were confirmed in experiments using RelA^–/– murine embryonic fibroblasts reconstituted with a RelA Ser²⁷⁶Ala mutation. In addition, we observe that phospho-Ser²⁷⁶ RelA binds the positive transcription elongation factor b (P-TEFb), a complex containing the cyclin-dependent kinase 9 (CDK-9) and cyclin T1 subunits. Inhibition of P-TEFb activity by short interfering RNA (siRNA)-mediated knockdown shows that the phospho-Ser²⁷⁶ RelA-P-TEFb complex is required for IL-8 and Gro-β gene activation but not for IB gene activation. These studies indicate that TNF induces target gene expression by heterogeneous mechanisms. One is mediated by phospho-Ser²⁷⁶ RelA formation and chromatin targeting of P-TEFb controlling polymerase II (Pol II) recruitment and carboxy-terminal domain phosphorylation on the IL-8 and Gro-β genes. The second involves a phospho-Ser²⁷⁶ RelA-independent activation of genes preloaded with Pol II, exemplified by the IB gene. Together, these data suggest that the binding kinetics, selection of genomic targets, and mechanisms of promoter induction by RelA are controlled by a phosphorylation code influencing its interactions with coactivators and transcriptional elongation factors.

Published ahead of print on 24 March 2008.

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

These authors contributed equally to this work.