Hartman Institute for Therapeutic Organ Regeneration

The bHLH transcription factors OLIG2 and OLIG1 couple neuronal and glial subtype specification.

TitleThe bHLH transcription factors OLIG2 and OLIG1 couple neuronal and glial subtype specification.
Publication TypeJournal Article
Year of Publication2002
AuthorsZhou Q, Anderson DJ
JournalCell
Volume109
Issue1
Pagination61-73
Date Published2002 Apr 05
ISSN0092-8674
KeywordsAnimals, Astrocytes, Basic Helix-Loop-Helix Transcription Factors, Cell Differentiation, Cell Lineage, DNA-Binding Proteins, Female, Helix-Loop-Helix Motifs, Homeodomain Proteins, Interneurons, Male, Mice, Mice, Knockout, Motor Neurons, Mutation, Nerve Tissue Proteins, Neuroglia, Neurons, Oligodendrocyte Transcription Factor 2, Oligodendroglia, Rhombencephalon, Spinal Cord, Stem Cells, Transcription Factors
Abstract

OLIG1 and OLIG2 are basic-helix-loop-helix (bHLH) transcription factors expressed in the pMN domain of the spinal cord, which sequentially generates motoneurons and oligodendrocytes. In Olig1/2 double-mutant mice, motoneurons are largely eliminated, and oligodendrocyte differentiation is abolished. Lineage tracing data suggest that Olig1(-/-)2(-/-) pMN progenitors instead generate V2 interneurons and then astrocytes. This apparent conversion likely reflects independent roles for OLIG1/2 in specifying motoneuron and oligodendrocyte fates. Olig genes therefore couple neuronal and glial subtype specification, unlike proneural bHLH factors that control the neuron versus glia decision. Our results suggest that in the spinal cord, Olig and proneural genes comprise a combinatorial code for the specification of neurons, astrocytes, and oligodendrocytes, the three fundamental cell types of the central nervous system.

DOI10.1016/s0092-8674(02)00677-3
Alternate JournalCell
PubMed ID11955447
Grant ListR01-NS23476 / NS / NINDS NIH HHS / United States

Weill Cornell Medicine
Hartman Institute for Therapeutic Organ Regeneration
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