I?B? is the major inhibitor of NF-?B, a family of transcription factors that control transcription of many inflammation-related genes. On the one hand, wounds and infections would never heal without proper inflammation;on the other hand, inflammation has long been associated with the development of cancer, especially metastasis. Therefore, the control of NF-?B transcriptional function is critical for human health. I?B? is a major inhibitor of NF-?B. Inflammatory stimuli, such as cytokines or infections, can trigger rapid degradation of I?B? via the ubiquitin-proteasome pathway. Consequently, NF-?B is activated to transcribe a spectrum of genes related to inflammatory responses. It has been shown that the SCF?TRCP ubiquitin ligase ubiquitinates I?B? upon stimulation. However, little is known about the post-ubiquitinational events of I?B? proteolysis. Polyubiquitinated I?B? still associates with NF-?B, indicating that ubiquitination of I?B? alone is not sufficient to release the inhibitory functin of I?B?. Therefore, the post-ubiquitinational regulation of I?B? is essential for I?B? turnover and NF-?B activation. Understanding this process could pioneer novel therapies to regulate inflammation. Recent studies in our lab suggest that a valosin-containing protein (VCP) and its cofactor, UFD1L, are involved in post-ubiquitinational regulation of I?B?. In this proposal, we wil dissect the mechanisms by which the VCP protein complex regulates I?B? post-ubiquitination. We will also strive to understand how the VCP complex delivers ubiquitinated I?B? to the 26S proteasome, and how the polyubiquitin receptors and deubiquitin enzyme (DUB) are involved in I?B? turnover and NF-?B activation.

Public Health Relevance

I?B? is the major inhibitor of NF-?B, a family of transcription factors that control transcription of many inflammation-related genes. Post-ubiquitinational regulation of I?B? is an important process that contributes to NF-?B and inflammation control.

National Institute of Health (NIH)
National Institute of General Medical Sciences (NIGMS)
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Cellular Signaling and Regulatory Systems Study Section (CSRS)
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Gaillard, Shawn R
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University of Texas Health Science Center Houston
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