PT  - JOURNAL ARTICLE
AU  - Cristina Gutiérrez-Caballero
AU  - Selena G. Burgess
AU  - Richard Bayliss
AU  - Stephen J. Royle
TI  - TACC3–ch-TOG track the growing tips of microtubules independently of clathrin and Aurora-A phosphorylation
AID  - 10.1101/008359
DP  - 2014 Jan 01
TA  - bioRxiv
PG  - 008359
4099  - http://biorxiv.org/content/early/2014/11/04/008359.short
4100  - http://biorxiv.org/content/early/2014/11/04/008359.full
AB  - The interaction between TACC3 (transforming acidic coiled coil protein 3) and the microtubule polymerase ch-TOG (colonic, hepatic tumor overexpressed gene) is evolutionarily conserved. Loading of TACC3–ch-TOG onto mitotic spindle microtubules requires the phosphorylation of TACC3 by Aurora-A kinase and the subsequent interaction of TACC3 with clathrin to form a microtubule-binding surface. Recent work indicates that TACC3 can track the plus-ends of microtubules and modulate microtubule dynamics in non-dividing cells via its interaction with ch-TOG. Whether there is a pool of TACC3–ch-TOG that is independent of clathrin in human cells, and what is the function of this pool, are open questions. Here, we describe the molecular interaction between TACC3 and ch-TOG that permits TACC3 recruitment to the plus-ends of microtubules. This TACC3–ch-TOG pool is independent of EB1, EB3, Aurora-A phosphorylation and binding to clathrin. We also describe the distinct combinatorial subcellular pools of TACC3, ch-TOG and clathrin. TACC3 is often described as a centrosomal protein, but we show that there is no significant population of TACC3 at centrosomes. The delineation of distinct protein pools reveals a simplified view of how these proteins are organized and controlled by post-translational modification.