학술논문

Olig1 Function Is Required to Repress Dlx1/2 and Interneuron Production in Mammalian Brain
Document Type
article
Source
Neuron. 81(3)
Subject
Biological Psychology
Biomedical and Clinical Sciences
Psychology
Stem Cell Research
Mental Health
Brain Disorders
Genetics
Neurosciences
Stem Cell Research - Nonembryonic - Non-Human
1.1 Normal biological development and functioning
Underpinning research
Neurological
Action Potentials
Age Factors
Animals
Basic Helix-Loop-Helix Transcription Factors
Brain
Cell Count
DNA-Binding Proteins
Embryo
Mammalian
Gene Expression Regulation
Developmental
Glutamate Decarboxylase
Homeodomain Proteins
Interneurons
Mice
Mice
Inbred C57BL
Mice
Transgenic
Mutation
Nerve Tissue Proteins
Neuropeptides
Organ Culture Techniques
Patch-Clamp Techniques
Synapses
Transcription Factors
Cognitive Sciences
Neurology & Neurosurgery
Biological psychology
Language
Abstract
Abnormal GABAergic interneuron density, and imbalance of excitatory versus inhibitory tone, is thought to result in epilepsy, neurodevelopmental disorders, and psychiatric disease. Recent studies indicate that interneuron cortical density is determined primarily by the size of the precursor pool in the embryonic telencephalon. However, factors essential for regulating interneuron allocation from telencephalic multipotent precursors are poorly understood. Here we report that Olig1 represses production of GABAergic interneurons throughout the mouse brain. Olig1 deletion in mutant mice results in ectopic expression and upregulation of Dlx1/2 genes in the ventral medial ganglionic eminences and adjacent regions of the septum, resulting in an ∼30% increase in adult cortical interneuron numbers. We show that Olig1 directly represses the Dlx1/2 I12b intergenic enhancer and that Dlx1/2 functions genetically downstream of Olig1. These findings establish Olig1 as an essential repressor of Dlx1/2 and interneuron production in developing mammalian brain.