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Nat Neurosci. 2012 Jan 15;15(3):381-8, S1. doi: 10.1038/nn.3026.

PSD-95 is post-transcriptionally repressed during early neural development by PTBP1 and PTBP2.

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1
Howard Hughes Medical Institute, University of California at Los Angeles, Los Angeles, California, USA.

Abstract

Postsynaptic density protein 95 (PSD-95) is essential for synaptic maturation and plasticity. Although its synaptic regulation has been widely studied, the control of PSD-95 cellular expression is not understood. We found that Psd-95 was controlled post-transcriptionally during neural development. Psd-95 was transcribed early in mouse embryonic brain, but most of its product transcripts were degraded. The polypyrimidine tract binding proteins PTBP1 and PTBP2 repressed Psd-95 (also known as Dlg4) exon 18 splicing, leading to premature translation termination and nonsense-mediated mRNA decay. The loss of first PTBP1 and then of PTBP2 during embryonic development allowed splicing of exon 18 and expression of PSD-95 late in neuronal maturation. Re-expression of PTBP1 or PTBP2 in differentiated neurons inhibited PSD-95 expression and impaired the development of glutamatergic synapses. Thus, expression of PSD-95 during early neural development is controlled at the RNA level by two PTB proteins whose sequential downregulation is necessary for synapse maturation.

PMID:
22246437
PMCID:
PMC3288398
DOI:
10.1038/nn.3026
[Indexed for MEDLINE]
Free PMC Article

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