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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
Author(s) -
Mala V. Rao,
Panaiyur S. Mohan,
Asok Kumar,
Aidong Yuan,
Lee Montagna,
Jabbar Campbell,
Veeranna,
Enilza Maria Espreáfico,
J.P. Julien,
Ralph A. Nixon
Publication year - 2011
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0017087
Subject(s) - endoplasmic reticulum , organelle , axon , microbiology and biotechnology , myosin , protein subunit , neurofilament , biology , axoplasmic transport , biophysics , chemistry , biochemistry , immunohistochemistry , gene , immunology
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.

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