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Open AccessJournal ArticleDOI

SMRT Derepression by the IκB Kinase α: A Prerequisite to NF-κB Transcription and Survival

Jamie E. Hoberg, +2 more
- 22 Oct 2004 - 
- Vol. 16, Iss: 2, pp 245-255
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TLDR
In this paper, the authors demonstrate that NF-κB transcription requires IKKα to phosphorylate SMRT on chromatin, stimulating the exchange of corepressor for coactivator complexes.
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This article is published in Molecular Cell.The article was published on 2004-10-22 and is currently open access. It has received 221 citations till now. The article focuses on the topics: Derepression & Corepressor.

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Citations
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Journal ArticleDOI

Integrating cell-signalling pathways with NF-kappaB and IKK function.

TL;DR: This work has shown that crosstalk constitutes a decision-making process that determines the consequences of NF-κB and IKK activation and, ultimately, cell fate.
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A SUMOylation-dependent pathway mediates transrepression of inflammatory response genes by PPAR-gamma.

TL;DR: This mechanism provides an explanation for how an agonist-bound nuclear receptor can be converted from an activator of transcription to a promoter-specific repressor of NF-κB target genes that regulate immunity and homeostasis.
Journal ArticleDOI

New regulators of NF-kappaB in inflammation.

TL;DR: This Review discusses new insights into the regulation of NF-κB, a key mediator of inducible transcription in the immune system, that have been identified and some of the known components have been assigned new roles.
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Sensors and signals: a coactivator/corepressor/epigenetic code for integrating signal-dependent programs of transcriptional response.

TL;DR: This strategy imposes a temporal order for modifying programs of transcriptional regulation in response to the cellular milieu, which is used to mediate developmental/homeostatic and pathological events.
Journal ArticleDOI

Post-translational modifications regulating the activity and function of the nuclear factor kappa B pathway

TL;DR: Understanding these pathways will not only provide valuable insights into mechanism and function, but could also lead to new drug targets and the development of diagnostic and prognostic biomarkers for many pathological conditions.
References
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Journal ArticleDOI

THE NF-κB AND IκB PROTEINS: New Discoveries and Insights

TL;DR: The transcription factor NF-κB has attracted widespread attention among researchers in many fields based on its unusual and rapid regulation, the wide range of genes that it controls, its central role in immunological processes, the complexity of its subunits, and its apparent involvement in several diseases.
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Missing Pieces in the NF-κB Puzzle

TL;DR: In this paper, a review of recent progress as well as unanswered questions regarding the regulation and function of NF-kappaB and IKK is presented, focusing on recent progress and unanswered questions.
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NF-κB at the crossroads of life and death

TL;DR: The choice between life and death is one of the major events in regulation of the immune system and a major regulator of such life or death decisions is the transcription factor NF-κB as mentioned in this paper.
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Modulation of NF-κB-dependent transcription and cell survival by the SIRT1 deacetylase

TL;DR: It is demonstrated that SIRT1, a nicotinamide adenosine dinucleotide‐dependent histone deacetylase, regulates the transcriptional activity of NF‐κB and activity augments apoptosis in response to TNFα.
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The Myc/Max/Mad Network and the Transcriptional Control of Cell Behavior

TL;DR: The Myc/Max/Mad network comprises a group of transcription factors whose distinct interactions result in gene-specific transcriptional activation or repression and can be viewed as a functional module which acts to convert environmental signals into specific gene-regulatory programs.
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