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The Journal of Neuroscience, January 1, 1998, 18(1):251-265

Sorting of beta -Actin mRNA and Protein to Neurites and Growth Cones in Culture

Gary J. Bassell1, Honglai Zhang1, Anne L. Byrd1, Andrea M. Femino1, Robert H. Singer1, Krishan L. Taneja2, Lawrence M. Lifshitz3, Ira M. Herman4, and Kenneth S. Kosik5

1 Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461, 2 Department of Cell Biology and 3 Biomedical Imaging Group, University of Massachusetts Medical Center, Worcester, Massachusetts 10615, 4 Department of Physiology, Tufts University School of Medicine, Boston, Massachusetts, and 5 Center for Neurological Disease, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts

The transport of mRNAs into developing dendrites and axons may be a basic mechanism to localize cytoskeletal proteins to growth cones and influence microfilament organization. Using isoform-specific antibodies and probes for in situ hybridization, we observed distinct localization patterns for beta - and gamma -actin within cultured cerebrocortical neurons. beta -Actin protein was highly enriched within growth cones and filopodia, in contrast to gamma -actin protein, which was distributed uniformly throughout the cell. beta -Actin protein also was shown to be peripherally localized after transfection of beta -actin cDNA bearing an epitope tag. beta -Actin mRNAs were localized more frequently to neuronal processes and growth cones, unlike gamma -actin mRNAs, which were restricted to the cell body. The rapid localization of beta -actin mRNA, but not gamma -actin mRNA, into processes and growth cones could be induced by dibutyryl cAMP treatment. Using high-resolution in situ hybridization and image-processing methods, we showed that the distribution of beta -actin mRNA within growth cones was statistically nonrandom and demonstrated an association with microtubules. beta -Actin mRNAs were detected within minor neurites, axonal processes, and growth cones in the form of spatially distinct granules that colocalized with translational components. Ultrastructural analysis revealed polyribosomes within growth cones that colocalized with cytoskeletal filaments. The transport of beta -actin mRNA into developing neurites may be a sequence-specific mechanism to synthesize cytoskeletal proteins directly within processes and growth cones and would provide an additional means to deliver cytoskeletal proteins over long distances.

Key words: mRNA localization; actin isoforms; cytoskeleton; growth cones; axonal transport; in situ hybridization


Copyright © 1998 Society for Neuroscience  0270-6474/98/181251-15$05.00/0


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W. Gu, F. Pan, H. Zhang, G. J. Bassell, and R. H. Singer
A predominantly nuclear protein affecting cytoplasmic localization of {beta}-actin mRNA in fibroblasts and neurons
J. Cell Biol., January 7, 2002; 156(1): 41 - 52.
[Abstract] [Full Text] [PDF]


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Mol. Biol. CellHome page
G. Liu, W. M. Grant, D. Persky, V. M. Latham Jr., R. H. Singer, and J. Condeelis
Interactions of Elongation Factor 1alpha with F-Actin and beta -Actin mRNA: Implications for Anchoring mRNA in Cell Protrusions
Mol. Biol. Cell, February 1, 2002; 13(2): 579 - 592.
[Abstract] [Full Text] [PDF]



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