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The myosin Va head domain binds to the neurofilament-L rod and modulates endoplasmic reticulum (ER) content and distribution within axons.

Publication Type:

Journal Article

Source:

PLoS One, Volume 6, Issue 2, p.e17087 (2011)

Keywords:

Animals, Axons, Endoplasmic Reticulum, Intermediate Filaments, Mice, Mice, Inbred C57BL, Mice, Knockout, Myosin Heavy Chains, Myosin Type V, Neurofilament Proteins, Neurons, Protein Binding, Protein Structure, Tertiary, Tissue Distribution

Abstract:

<p>The neurofilament light subunit (NF-L) binds to myosin Va (Myo Va) in neurons but the sites of interaction and functional significance are not clear. We show by deletion analysis that motor domain of Myo Va binds to the NF-L rod domain that forms the NF backbone. Loss of NF-L and Myo Va binding from axons significantly reduces the axonal content of ER, and redistributes ER to the periphery of axon. Our data are consistent with a novel function for NFs as a scaffold in axons for maintaining the content and proper distribution of vesicular organelles, mediated in part by Myo Va. Based on observations that the Myo Va motor domain binds to intermediate filament (IF) proteins of several classes, Myo Va interactions with IFs may serve similar roles in organizing organelle topography in different cell types.</p>

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