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The Caenorhabditis elegans Elongator Complex Regulates Neuronal α-tubulin Acetylation
Author(s) -
Jachen A. Solinger,
Roberta Paolinelli,
Holger Klöß,
Francesco Berlanda Scorza,
Stefano Marchesi,
Ursula Sauder,
Dai Mitsushima,
Fabrizio Capuani,
Stephen R. Stürzenbaum,
Giuseppe Cassata
Publication year - 2010
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/journal.pgen.1000820
Subject(s) - biology , acetylation , caenorhabditis elegans , acetyltransferase , microtubule , tubulin , microbiology and biotechnology , protein subunit , mutant , genetics , gene
Although acetylated α-tubulin is known to be a marker of stable microtubules in neurons, precise factors that regulate α-tubulin acetylation are, to date, largely unknown. Therefore, a genetic screen was employed in the nematode Caenorhabditis elegans that identified the Elongator complex as a possible regulator of α-tubulin acetylation. Detailed characterization of mutant animals revealed that the acetyltransferase activity of the Elongator is indeed required for correct acetylation of microtubules and for neuronal development. Moreover, the velocity of vesicles on microtubules was affected by mutations in Elongator. Elongator mutants also displayed defects in neurotransmitter levels. Furthermore, acetylation of α-tubulin was shown to act as a novel signal for the fine-tuning of microtubules dynamics by modulating α-tubulin turnover, which in turn affected neuronal shape. Given that mutations in the acetyltransferase subunit of the Elongator (Elp3) and in a scaffold subunit (Elp1) have previously been linked to human neurodegenerative diseases, namely Amyotrophic Lateral Sclerosis and Familial Dysautonomia respectively highlights the importance of this work and offers new insights to understand their etiology.

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