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Journal of Biological Chemistry
Article . 2001 . Peer-reviewed
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Journal of Biological Chemistry
Article
License: CC BY
Data sources: UnpayWall
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N-Methyl-d-aspartate Receptors Regulate a Group of Transiently Expressed Genes in the Developing Brain

Authors: Roderick A. Corriveau; Rajan G. Patel; Naoaki Sugiura;

N-Methyl-d-aspartate Receptors Regulate a Group of Transiently Expressed Genes in the Developing Brain

Abstract

Mammalian brain development requires the transmission of electrical signals between neurons via the N-methyl-d-aspartate (NMDA) class of glutamate receptors. However, little is known about how NMDA receptors carry out this role. Here we report the first genes shown to be regulated by physiological levels of NMDA receptor function in developing neurons in vivo: NMDA receptor-regulated gene 1 (NARG1), NARG2, and NARG3. These genes share several striking regulatory features. All three are expressed at high levels in the neonatal brain in regions of neuronal proliferation and migration, are dramatically down-regulated during early postnatal development, and are down-regulated by NMDA receptor function. NARG2 and NARG3 appear to be novel, while NARG1 is the mammalian homologue of a yeast N-terminal acetyltransferase that regulates entry into the G(o) phase of the cell cycle. The results suggest that highly specific NMDA receptor-dependent regulation of gene expression plays an important role in the transition from proliferation of neuronal precursors to differentiation of neurons.

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Keywords

Expressed Sequence Tags, Mice, Knockout, Neurons, DNA, Complementary, Cell Cycle, Brain, Down-Regulation, Gene Expression Regulation, Developmental, Nerve Tissue Proteins, Blotting, Northern, Mice, Acetyltransferases, Cell Movement, Animals, Drosophila, N-Terminal Acetyltransferase E, Cell Division, In Situ Hybridization, N-Terminal Acetyltransferase A, Gene Library

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    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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    influence
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citations
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!
52
Top 10%
Top 10%
Top 10%
gold