Sign in
Cancer BiologybioRxiv
Preprint

The MYC antagonist MNT autoregulates its expression and supports proliferation in MAX deficient cells

M Carmen Lafita-Navarro, Judit Liaño-Pons, Andrea Quintanilla, Ignacio Varela, Fabiana Ourique, Gabriel Bretones, Rosa Blanco, Julia Aresti, Patrick Carroll, Peter Hurlin, Robert N. Eisenman, M. Dolores Delgado, Javier León

Abstract

MNT is a transcription factor of the MXD family. MNT-MAX dimers down-regulate genes by binding to E-box sequences, which can also be bound by MYC-MAX to activate transcription. MNT has been described as a modulator of MYC activity but little is known about MNT regulation and whether MNT has MAX-independent functions. Using a MAX deficient cell line and siRNA-mediated silencing of MAX, we show that in the absence of MAX, the total MNT levels are elevated and that MNT localizes both in the cytoplasm and the nucleus. In contrast, MNT is predominantly nuclear when MAX is expressed. MNT is required for optimal cell proliferation even in the absence of MAX, being the first report of a MAX-independent function of MNT. Interestingly, MNT forms homodimers and autoregulates its expression by repressing its own promoter. The tight MNT regulation and its activity in absence of MAX suggest its importance on cell homeostasis.

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.