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Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes

Authors: Stacey M Glasgow; Wenyi Zhu; C Claus Stolt; Teng-Wei Huang; Fuyi Chen; Joseph J LoTurco; Jeffrey L Neul; +3 Authors

Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes

Abstract

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.

Keywords

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

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    influence
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    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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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).
BIP!Citations provided by BIP!
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.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
137
Top 1%
Top 10%
Top 1%
Green
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