Chemogenetic tuning reveals optimal MAPK signaling for cell-fate programming

Cell states evolve through the combined activity of signaling pathways and gene regulatory networks. While transcription factors can direct cell fate, these factors rely on a cell state that is receptive to transitions in cell identity. How signaling levels contribute to the emergence of receptive cell states remains poorly defined in primary cells. Using a well-defined model of direct conversion, we examined how levels of the MAPK-activating oncogene HRASG12V influence direct conversion of primary fibroblasts to induced motor neurons. We demonstrate that an optimal Goldilocks level of MAPK signaling efficiently drives cell-fate programming. Rates of direct conversion respond biphasically to increasing HRASG12V levels. While intermediate HRASG12V levels increase the rate of conversion, high levels of HRASG12V induce senescence. Through chemogenetic tuning, we set optimal MAPK activity for high rates of conversion in the absence of HRAS mutants. As MAPK pathways influence cell-fate transitions in development and disease, our results highlight the need to tune therapeutic interventions within a non-monotonic landscape that is shaped by genetics and levels of gene expression. HighlightsO_LIMAPK signaling drives proliferation and conversion of fibroblasts to motor neurons C_LIO_LICell-fate programming responds biphasically to HRASG12V expression C_LIO_LIHigh HRASG12V expression induces senescence, which reduces conversion C_LIO_LIChemogenetic tuning of MAPK activity increases conversion rates C_LIO_LIA small-molecule MAPK inducer drives high rates of conversion in the absence of HRASG12V C_LI