4.7 Article

BDNF regulates the translation of a select group of mRNAs by a mammalian target of rapamycin-phosphatidylinositol 3-kinase-dependent pathway during neuronal development

Journal

JOURNAL OF NEUROSCIENCE
Volume 24, Issue 33, Pages 7366-7377

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1739-04.2004

Keywords

BDNF; translation; microarray; axon guidance; synaptic plasticity; rapamycin

Categories

Funding

  1. NICHD NIH HHS [P30-HD18655, P30 HD018655] Funding Source: Medline
  2. NINDS NIH HHS [R37 NS028829, NS28829, R01 NS028829] Funding Source: Medline

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Local regulation of mRNA translation plays an important role in axon guidance, synaptic development, and neuronal plasticity. Little is known, however, regarding the mechanisms that control translation in neurons, and only a few mRNAs have been identified that are locally translated within axon and dendrites. Using Affymetrix gene arrays to identify mRNAs that are newly associated with polysomes after exposure to BDNF, we identified subsets of mRNAs for which translation is enhanced in neurons at different developmental stages. In mature neurons, many of these mRNAs encode proteins that are known to function at synapses, including CamKIIalpha, NMDA receptor subunits, and the postsynaptic density (PSD) scaffolding protein Homer2. BDNF regulates the translation of Homer2 locally in the synaptodendritic compartment by activating translational initiation via a mammalian target of rapamycin-phosphatidylinositol 3-kinase-dependent pathway. These findings suggest that BDNF likely regulates synaptic function by inducing the local synthesis of numerous synaptic proteins. The local translation of the cytoskeleton-associated protein Homer2 in particular might have important implications for growth cone dynamics and dendritic spine development.

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