| First Author | Li Y | Year | 2017 |
| Journal | J Cell Biol | Volume | 216 |
| Issue | 7 | Pages | 1975-1992 |
| PubMed ID | 28515277 | Mgi Jnum | J:246099 |
| Mgi Id | MGI:5920498 | Doi | 10.1083/jcb.201610014 |
| Citation | Li Y, et al. (2017) Histone chaperone HIRA regulates neural progenitor cell proliferation and neurogenesis via beta-catenin. J Cell Biol 216(7):1975-1992 |
| abstractText | Histone cell cycle regulator (HIRA) is a histone chaperone and has been identified as an epigenetic regulator. Subsequent studies have provided evidence that HIRA plays key roles in embryonic development, but its function during early neurogenesis remains unknown. Here, we demonstrate that HIRA is enriched in neural progenitor cells, and HIRA knockdown reduces neural progenitor cell proliferation, increases terminal mitosis and cell cycle exit, and ultimately results in premature neuronal differentiation. Additionally, we demonstrate that HIRA enhances beta-catenin expression by recruiting H3K4 trimethyltransferase Setd1A, which increases H3K4me3 levels and heightens the promoter activity of beta-catenin. Significantly, overexpression of HIRA, HIRA N-terminal domain, or beta-catenin can override neurogenesis abnormities caused by HIRA defects. Collectively, these data implicate that HIRA, cooperating with Setd1A, modulates beta-catenin expression and then regulates neurogenesis. This finding represents a novel epigenetic mechanism underlying the histone code and has profound and lasting implications for diseases and neurobiology. |
