
Lineage progression and diversification is regulated by the coordinated action of unique sets of transcription factors. Oligodendrocytes (OL) and astrocytes (AS) comprise the glial sub-lineages in the CNS, and the manner in which their associated regulatory factors orchestrate lineage diversification during development and disease remains an open question. Sox10 and NFIA are key transcriptional regulators of gliogenesis associated with OL and AS. We found that NFIA inhibited Sox10 induction of OL differentiation through direct association and antagonism of its function. Conversely, we found that Sox10 antagonized NFIA function and suppressed AS differentiation in mouse and chick systems. Using this developmental paradigm as a model for glioma, we found that this relationship similarly regulated the generation of glioma subtypes. Our results describe the antagonistic relationship between Sox10 and NFIA that regulates the balance of OL and AS fate during development and demonstrate for the first time, to the best of our knowledge, that the transcriptional processes governing glial sub-lineage diversification oversee the generation of glioma subtypes.
Chromatin Immunoprecipitation, 1.1 Normal biological development and functioning, Cells, Biological Psychology, Green Fluorescent Proteins, Nerve Tissue Proteins, Chick Embryo, Transfection, Article, Mice, Rare Diseases, Underpinning research, Genetics, Basic Helix-Loop-Helix Transcription Factors, Psychology, Animals, Cells, Cultured, Cancer, Cerebral Cortex, Homeodomain Proteins, Cultured, Neurology & Neurosurgery, Biomedical and Clinical Sciences, SOXE Transcription Factors, Mammalian, Neurosciences, Cell Differentiation, Myelin Basic Protein, Glioma, Oligodendrocyte Transcription Factor 2, Stem Cell Research, Newborn, Embryo, Mammalian, Brain Disorders, Brain Cancer, NFI Transcription Factors, Electroporation, Animals, Newborn, Embryo, Neurological, Biological psychology, Stem Cell Research - Nonembryonic - Non-Human, Cognitive Sciences, Neuroglia
Chromatin Immunoprecipitation, 1.1 Normal biological development and functioning, Cells, Biological Psychology, Green Fluorescent Proteins, Nerve Tissue Proteins, Chick Embryo, Transfection, Article, Mice, Rare Diseases, Underpinning research, Genetics, Basic Helix-Loop-Helix Transcription Factors, Psychology, Animals, Cells, Cultured, Cancer, Cerebral Cortex, Homeodomain Proteins, Cultured, Neurology & Neurosurgery, Biomedical and Clinical Sciences, SOXE Transcription Factors, Mammalian, Neurosciences, Cell Differentiation, Myelin Basic Protein, Glioma, Oligodendrocyte Transcription Factor 2, Stem Cell Research, Newborn, Embryo, Mammalian, Brain Disorders, Brain Cancer, NFI Transcription Factors, Electroporation, Animals, Newborn, Embryo, Neurological, Biological psychology, Stem Cell Research - Nonembryonic - Non-Human, Cognitive Sciences, Neuroglia
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 137 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
