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• W2089543102 abstract "Rab proteins influence vesicle trafficking pathways through the assembly of regulatory protein complexes. Previous investigations have documented that Rab11a and Rab8a can interact with the tail region of myosin Vb and regulate distinct trafficking pathways. We have now determined that a related Rab protein, Rab10, can interact with myosin Va, myosin Vb, and myosin Vc. Rab10 localized to a system of tubules and vesicles that have partially overlapping localization with Rab8a. Both Rab8a and Rab10 were mislocalized by the expression of dominant-negative myosin V tails. Interaction with Rab10 was dependent on the presence of the alternatively spliced exon D in myosin Va and myosin Vb and the homologous region in myosin Vc. Yeast two-hybrid assays and fluorescence resonance energy transfer studies confirmed that Rab10 binding to myosin V tails in vivo required the alternatively spliced exon D. In contrast to our previous work, we found that Rab11a can interact with both myosin Va and myosin Vb tails independent of their splice isoform. These results indicate that Rab GTPases regulate diverse endocytic trafficking pathways through recruitment of multiple myosin V isoforms." @default.
• W2089543102 created "2016-06-24" @default.
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• W2089543102 date "2009-01-01" @default.
• W2089543102 modified "2023-09-29" @default.
• W2089543102 title "Alternative Splicing in Class V Myosins Determines Association with Rab10" @default.
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• W2089543102 doi "https://doi.org/10.1074/jbc.m805957200" @default.
• W2089543102 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2613619" @default.
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