Structural and functional analysis of the related transcriptional enhancer factor-1 and NF-?B interaction.

ABSTRACT: The related transcriptional enhancer factor-1 (RTEF-1) increases gene transcription of hypoxia-inducible factor 1? (HIF-1?) and enhances angiogenesis in endothelium. Both hypoxia and inflammatory factor TNF-? regulate gene expression of HIF-1?, but how RTEF-1 and TNF-? coordinately regulate HIF-1? gene transcription is unclear. Here, we found that RTEF-1 interacts with p65 subunit of NF-?B, a primary mediator of TNF-?. RTEF-1 increased HIF-1? promoter activity, whereas expression of p65 subunit inhibited the stimulatory effect. By contrast, knockdown of p65 markedly enhanced RTEF-1 stimulation on the HIF-1? promoter activity (7-fold). A physical interaction between RTEF-1 and p65 was confirmed by coimmunoprecipitation experiments in cells and glutathione S-transferase (GST)-pull-down assays. A computational analysis of RTEF-1 crystal structures revealed that a conserved surface of RTEF-1 potentially interacts with p65 via four amino acid residues located at T347, Y349, R351, and Y352. We performed site-directed mutagenesis and GST-pull-down assays and demonstrated that Tyr352 (Y352) in RTEF-1 is a key site for the formation of RTEF-1 and p65-NF-?B complex. An alanine mutation at Y352 of RTEF-1 disrupted the interaction of RTEF-1 with p65. Moreover, expression of RTEF-1 decreased TNF-?-induced HIF-1? promoter activity, IL-1?, and IL-6 mRNA levels in cells; however, the effect of RTEF-1 was largely lost when Y352 was mutated to alanine. These results indicate that RTEF-1 interacts with p65-NF-?B through Y352 and that they antagonize each other for HIF-1? transcriptional activation, suggesting a novel mechanism by which RTEF-1 regulates gene expression, linking hypoxia to inflammation.

SUBMITTER: Ma J 

PROVIDER: S-EPMC3920133 | biostudies-literature | 2014 Jan

REPOSITORIES: biostudies-literature