| First Author | Oshikawa M | Year | 2017 |
| Journal | Development | Volume | 144 |
| Issue | 18 | Pages | 3303-3314 |
| PubMed ID | 28928282 | Mgi Jnum | J:263656 |
| Mgi Id | MGI:5918288 | Doi | 10.1242/dev.154013 |
| Citation | Oshikawa M, et al. (2017) Dnmt1-dependent Chk1 pathway suppression is protective against neuron division. Development 144(18):3303-3314 |
| abstractText | Neuronal differentiation and cell-cycle exit are tightly coordinated, even in pathological situations. When pathological neurons re-enter the cell cycle and progress through the S phase, they undergo cell death instead of division. However, the mechanisms underlying mitotic resistance are mostly unknown. Here, we have found that acute inactivation of retinoblastoma (Rb) family proteins (Rb, p107 and p130) in mouse postmitotic neurons leads to cell death after S-phase progression. Checkpoint kinase 1 (Chk1) pathway activation during the S phase prevented the cell death, and allowed the division of cortical neurons that had undergone acute Rb family inactivation, oxygen-glucose deprivation (OGD) or in vivo hypoxia-ischemia. During neurogenesis, cortical neurons became protected from S-phase Chk1 pathway activation by the DNA methyltransferase Dnmt1, and underwent cell death after S-phase progression. Our results indicate that Chk1 pathway activation overrides mitotic safeguards and uncouples neuronal differentiation from mitotic resistance. |
