Muroyama Andrew, Seldin Lindsey, Lechler Terry
Department of Dermatology, Duke University Medical Center, Durham, NC 27710 Department of Cell Biology, Duke University Medical Center, Durham, NC 27710.
Department of Dermatology, Duke University Medical Center, Durham, NC 27710 Department of Cell Biology, Duke University Medical Center, Durham, NC 27710
J Cell Biol. 2016 Jun 20;213(6):679-92. doi: 10.1083/jcb.201601099. Epub 2016 Jun 13.
Differentiation induces the formation of noncentrosomal microtubule arrays in diverse tissues. The formation of these arrays requires loss of microtubule-organizing activity (MTOC) at the centrosome, but the mechanisms regulating this transition remain largely unexplored. Here, we use the robust loss of centrosomal MTOC activity in the epidermis to identify two pools of γ-tubulin that are biochemically and functionally distinct and differentially regulated. Nucleation-competent CDK5RAP2-γ-tubulin complexes were maintained at centrosomes upon initial epidermal differentiation. In contrast, Nedd1-γ-tubulin complexes did not promote nucleation but were required for anchoring of microtubules, a previously uncharacterized activity for this complex. Cell cycle exit specifically triggered loss of Nedd1-γ-tubulin complexes, providing a mechanistic link connecting MTOC activity and differentiation. Collectively, our studies demonstrate that distinct γ-tubulin complexes regulate different microtubule behaviors at the centrosome and show that differential regulation of these complexes drives loss of centrosomal MTOC activity.
分化诱导多种组织中非中心体微管阵列的形成。这些阵列的形成需要中心体处微管组织活性(MTOC)的丧失,但调节这种转变的机制在很大程度上仍未被探索。在这里,我们利用表皮中中心体MTOC活性的强烈丧失来鉴定两类在生化和功能上不同且受不同调节的γ-微管蛋白。有核能力的CDK5RAP2-γ-微管蛋白复合物在表皮初始分化时保留在中心体上。相比之下,Nedd1-γ-微管蛋白复合物不促进成核,但却是微管锚定所必需的,这是该复合物以前未被描述的活性。细胞周期退出特异性地触发了Nedd1-γ-微管蛋白复合物的丧失,提供了一个连接MTOC活性和分化的机制联系。总的来说,我们的研究表明,不同的γ-微管蛋白复合物在中心体调节不同的微管行为,并表明这些复合物的差异调节驱动了中心体MTOC活性的丧失。