Tubulin-binding cofactor B is a direct interaction partner of the dynactin subunit p150(Glued)

• Published in: Cell and tissue research Vol. 350; no. 1; pp. 13 - 26
• Main Authors: Kuh, Georges F, Stockmann, Marianne, Meyer-Ohlendorf, Marie, Linta, Leonhard, Proepper, Christian, Ludolph, Albert C, Bockmann, Juergen, Boeckers, Tobias M, Liebau, Stefan
• Format: Journal Article
• Language: English
• Published: Germany 01-10-2012
• Subjects: Animals; Cercopithecus aethiops; COS Cells; Down-Regulation - genetics; Dynactin Complex; Gene Expression Profiling; Gene Expression Regulation, Developmental; Gene Knockdown Techniques; HEK293 Cells; Humans; Intracellular Space - metabolism; Male; Microtubule-Associated Proteins - genetics; Microtubule-Associated Proteins - metabolism; Microtubules - metabolism; Neurons - cytology; Neurons - metabolism; Protein Binding - genetics; Protein Interaction Mapping; Protein Structure, Tertiary; Protein Subunits - genetics; Protein Subunits - metabolism; Protein Transport; Rats; RNA, Messenger - genetics; RNA, Messenger - metabolism; Synapses - metabolism
• ISSN: 1432-0878
• DOI: 10.1007/s00441-012-1463-z

The dynactin p150(Glued) subunit, encoded by the gene DCTN1, is part of the dynein-dynactin motor protein complex responsible for retrograde axonal transport in motor neurons. The p150 subunit is a candidate gene for neurodegenerative diseases, in particular motor neuron and extrapyramidal diseases. Tubulin-binding cofactors are believed to be involved in tubulin biogenesis and degradation and therefore to contribute to microtubule functional diversity and regulation. A yeast-two-hybrid screen for putative interacting proteins of dynactin p150(Glued) has revealed tubulin-folding cofactor B (TBCB). We analyzed the interaction of these proteins and investigated the impact of this complex on the microtubule network in cell lines and primary hippocampal neurons in vitro. We especially concentrated on neuronal morphology and synaptogenesis. Overexpression of both proteins or depletion of TBCB alone does not alter the microtubule network and/or neuronal morphology. The demonstration of the interaction of the transport molecule dynactin and the tubulin-regulating factor TBCB is thought to have an impact on several cellular mechanisms. TBCB expression levels have been found to have only a subtle influence on the microtubule network and neuronal morphology. However, overexpression of TBCB leads to the decreased localization of p150 to the microtubule network that might result in a functional modulation of this protein complex.