| First Author | Putra BP | Year | 2023 |
| Journal | Dev Growth Differ | Volume | 65 |
| Issue | 8 | Pages | 461-469 |
| PubMed ID | 37452641 | Mgi Jnum | J:344865 |
| Mgi Id | MGI:7579433 | Doi | 10.1111/dgd.12880 |
| Citation | Putra BP, et al. (2023) Pcgf1 gene disruption reveals primary involvement of epigenetic mechanism in neuronal subtype specification in the enteric nervous system. Dev Growth Differ 65(8):461-469 |
| abstractText | The enteric nervous system (ENS) regulates gut functions independently from the central nervous system (CNS) by its highly autonomic neural circuit that integrates diverse neuronal subtypes. Although several transcription factors are shown to be necessary for the generation of some enteric neuron subtypes, the mechanisms underlying neuronal subtype specification in the ENS remain elusive. In this study, we examined the biological function of Polycomb group RING finger protein 1 (PCGF1), one of the epigenetic modifiers, in the development and differentiation of the ENS by disrupting the Pcgf1 gene selectively in the autonomic-lineage cells. Although ENS precursor migration and enteric neurogenesis were largely unaffected, neuronal differentiation was impaired in the Pcgf1-deficient mice, with the numbers of neurons expressing somatostatin (Sst(+) ) decreased in multiple gut regions. Notably, the decrease in Sst(+) neurons was associated with the corresponding increase in calbindin(+) neurons in the proximal colon. These findings suggest that neuronal subtype conversion may occur in the absence of PCGF1, and that epigenetic mechanism is primarily involved in specification of some enteric neuron subtypes. |
