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A novel role of MNT as a negative regulator of REL and the NF-κB pathway
Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.07.21.210989v1?rss=1
Authors: Liano-Pons, J., Lafita-Navarro, M. C., Colomer, C., Garcia-Gaipo, L., Rodriguez, J., von Kriegsheim, A., Hurlin, P., Delgado, M. D., Bigas, A., Espinosa, L., Leon, J.
Abstract:
MNT, a transcription factor of the MXD family, is an important modulator of the oncoprotein MYC. Both MNT and MYC are basic-helix-loop-helix proteins that heterodimerize with MAX in a mutually exclusive manner, and bind to E-boxes within regulatory regions of their target genes. While MYC generally activates transcription, MNT represses it. However, the molecular interactions involving MNT as a transcriptional regulator beyond the binding to MAX remain unexplored. Here we demonstrate a novel MAX-independent protein interaction between MNT and c-REL (REL), the oncogenic member of the REL/NF-{kappa}B family. REL is involved in important biological processes and it is found altered in a variety of tumors. REL is a transcription factor that remains inactive in the cytoplasm in an inhibitory complex with I{kappa}B and translocates to the nucleus when the NF-{kappa}B pathway is activated. In the present manuscript, we show that MNT knockdown triggers REL translocation into the nucleus and thus the activation of the NF-{kappa}B pathway. Meanwhile, MNT overexpression results in the repression of I{kappa}B, a bona-fide REL target. Indeed, both MNT and REL bind to the I{kappa}B gene at a region mapping in the first exon, suggesting its regulation as a MNT-REL complex. Altogether our data indicate that MNT acts as a repressor of the NF-{kappa}B pathway by two different mechanisms: 1) retention of REL in the cytoplasm by MNT protein interaction and 2) MNT-driven repression of REL-target genes through a MNT-REL complex. These results widen our knowledge about MNT biological roles and reveal a novel connection between the MYC/MXD and the NF-{kappa}B pathways, two of the most prominent pathways involved in cancer.
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Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.07.21.210989v1?rss=1
Authors: Liano-Pons, J., Lafita-Navarro, M. C., Colomer, C., Garcia-Gaipo, L., Rodriguez, J., von Kriegsheim, A., Hurlin, P., Delgado, M. D., Bigas, A., Espinosa, L., Leon, J.
Abstract:
MNT, a transcription factor of the MXD family, is an important modulator of the oncoprotein MYC. Both MNT and MYC are basic-helix-loop-helix proteins that heterodimerize with MAX in a mutually exclusive manner, and bind to E-boxes within regulatory regions of their target genes. While MYC generally activates transcription, MNT represses it. However, the molecular interactions involving MNT as a transcriptional regulator beyond the binding to MAX remain unexplored. Here we demonstrate a novel MAX-independent protein interaction between MNT and c-REL (REL), the oncogenic member of the REL/NF-{kappa}B family. REL is involved in important biological processes and it is found altered in a variety of tumors. REL is a transcription factor that remains inactive in the cytoplasm in an inhibitory complex with I{kappa}B and translocates to the nucleus when the NF-{kappa}B pathway is activated. In the present manuscript, we show that MNT knockdown triggers REL translocation into the nucleus and thus the activation of the NF-{kappa}B pathway. Meanwhile, MNT overexpression results in the repression of I{kappa}B, a bona-fide REL target. Indeed, both MNT and REL bind to the I{kappa}B gene at a region mapping in the first exon, suggesting its regulation as a MNT-REL complex. Altogether our data indicate that MNT acts as a repressor of the NF-{kappa}B pathway by two different mechanisms: 1) retention of REL in the cytoplasm by MNT protein interaction and 2) MNT-driven repression of REL-target genes through a MNT-REL complex. These results widen our knowledge about MNT biological roles and reveal a novel connection between the MYC/MXD and the NF-{kappa}B pathways, two of the most prominent pathways involved in cancer.
Copy rights belong to original authors. Visit the link for more info