TY - JOUR T1 - Checkpoint signaling abrogation after cell cycle reentry reveals that differentiated neurons are mitotic cells JF - bioRxiv DO - 10.1101/288589 SP - 288589 AU - Chaska C Walton AU - Wei Zhang AU - Iris Patiño-Parrado AU - Estíbaliz Barrio-Alonso AU - Juan-José Garrido AU - José M Frade Y1 - 2018/01/01 UR - http://biorxiv.org/content/early/2018/04/17/288589.abstract N2 - A belief that has been central to biology for over a century is that neurons are not mitotic. However, how neurons are different from mitotic cells, if at all, remains unanswered. To this end, we have studied the extent to which the cell-cycle machinery of S, G2, and M-phases is functional in differentiated neurons. We have done this by using a fusion protein based on a truncated Cyclin E oncogenic isoform and Cdk2. Oncogenic Cyclin E/Cdk2 expression in primary neurons elicits canonical mitotic checkpoint signaling as in mitotic cells, resulting in cell-cycle arrest and neuronal cell-death. However, checkpoint suppression enables cell-cycle progression through S, G2, and M-phases and neuronal cell-division. We also show that neurons adapt to the cell-cycle by losing and reforming the axon initial segment, a structure essential to maintain neuronal viability. We conclude that neurons are mitotic cells in a reversible quiescent-like state, which is falsely portrayed as irreversible by mitotic checkpoints. ER -