Post-translational modification of tubulin serves as a powerful means for rapidly adjusting the functional diversity of microtubules. Acetylation of the Îμ -amino group of K40 in α-tubulin is one such modification that is highly conserved in ciliated organisms. Recently, αTAT1, a Gcn5-related N-acetyltransferase, was identified as an α-tubulin acetyltransferase in Tetrahymena and C. elegans. Here we generate mice with a targeted deletion of Atat1 to determine its function in mammals. Remarkably, we observe a loss of detectable K40 α-tubulin acetylation in these mice across multiple tissues and in cellular structures such as cilia and axons where acetylation is normally enriched. Mice are viable and develop normally, however, the absence of Atat1 impacts upon sperm motility and male mouse fertility, and increases microtubule stability. Thus, αTAT1 has a conserved function as the major α-tubulin acetyltransferase in ciliated organisms and has an important role in regulating subcellular specialization of subsets of microtubules.
|Titolo:||alpha TAT1 is the major alpha-tubulin acetyltransferase in mice|
|Autori:||Kalebic, Nereo; Sorrentino, Simona; Perlas, Emerald; Bolasco, Giulia; Martinez, Concepcion; Heppenstall, Paul A.|
|Data di pubblicazione:||2013|
|Numero di Articolo:||1962|
|Digital Object Identifier (DOI):||10.1038/ncomms2962|
|Appare nelle tipologie:||1.1 Journal article|