The majority of the α-tubulin in cultured neurons is acetylated (Black and Keyser, 1987). The present studies examine the relationships of the acetylation and deacetylation reactions to tubulin assembly and disassembly in intact neurons. Extraction assays which separate assembled and unassembled tubulin pools reveal that ≥99% of the total acetylated, as well as newly acetylated, tubulin is cytoskeletal associated. Treatment of neurons with depolymerizing drugs results in a progressive decrease in the levels of total tubulin in polymer and a corresponding increase in the levels of soluble tubulin. These drugs also cause a progressive decrease in the levels of acetylated α-tubulin in polymer that closely parallels in rate and extent that of total α-tubulin. However, there is no corresponding increase in soluble acetylated tubulin. Because the total levels of α-tubulin remain unchanged during drug treatment, the decrease in levels of acetylated α-tubulin during depolymerization must reflect its rapid conversion to nonacetylated α-tubulin. These findings suggest α-tubulin is acetylated in the polymeric form and that deacetylation is closely coupled to depolymerization. The close coupling between α-tubulin deacetylation and depolymerization provided a means of estimating the rate at which subunits cycle off microtubules in intact neurons. Acetate turnover on tubulin in intact neurons was determined both by pulse-chase protocols with 3H-acetate and by measuring the loss of acetylated subunits (using quantitative immunoblotting) under conditions of net microtubule depolymerization induced by colchicine. Both methods yielded similar results. Acetate turnover occurred biphasically; 30-50% of the acetate on tubulin turns over with a t( 1/2 ) of 1.5-2 hr, and the remaining half or more turns over with a t( 1/2 ) of 5-10 hr. We suggest that these kinetically distinguishable pools of acetylated α-tubulin reflect distinct pools of acetylated microtubules that differ in their average rates of subunit turnover.
CITATION STYLE
Black, M. M., Baas, P. W., & Humphries, S. (1989). Dynamics of α-tubulin deacetylation in intact neurons. Journal of Neuroscience, 9(1), 358–368. https://doi.org/10.1523/jneurosci.09-01-00358.1989
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