1. Academic Validation
  2. DDRGK1 regulates NF-κB activity by modulating IκBα stability

DDRGK1 regulates NF-κB activity by modulating IκBα stability

  • PLoS One. 2013 May 10;8(5):e64231. doi: 10.1371/journal.pone.0064231.
Peng Xi 1 Deqiang Ding Junzhi Zhou Miao Wang Yu-Sheng Cong
Affiliations

Affiliation

  • 1 Key Laboratory for Cell Proliferation and Regulation Biology of Ministry of Education, Institute of Cell Biology, College of Life Sciences, Beijing Normal University, Beijing, China.
Abstract

NF-κB is a ubiquitously expressed transcription factor that regulates a large number of genes in response to diverse physiological and pathological stimuli. The regulation of the transcriptional activity of NF-κB is often dependent on its interaction with IκBα. Proteins that bind to IκBα are critical regulators of NF-κB activity. DDRGK1 is a member of the DDRGK domain-containing protein family with unknown function. In this study, we showed that the depletion of DDRGK1 inhibits cell proliferation and invasion. Microarray analysis indicated that the expression of NF-κB target genes showed the most significant decrease after depleting of DDRGK1, suggesting that DDRGK1 may play an important role in the NF-κB signaling pathway. We further demonstrated that DDRGK1 interacts with IκBα and regulates its stability, thereby regulates the NF-κB transcriptional activity. Our findings identify DDRGK1 as an important regulator of the NF-κB pathway.

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