Divergent regulation of functionally distinct γ-tubulin complexes during differentiation

被引:58
|
作者
Muroyama, Andrew [1 ,2 ]
Seldin, Lindsey [1 ,2 ,3 ]
Lechler, Terry [1 ,2 ]
机构
[1] Duke Univ, Dept Dermatol, Med Ctr, Durham, NC 27710 USA
[2] Duke Univ, Dept Cell Biol, Med Ctr, Durham, NC 27710 USA
[3] Vanderbilt Univ, Dept Cell & Dev Biol, Nashville, TN 37203 USA
来源
JOURNAL OF CELL BIOLOGY | 2016年 / 213卷 / 06期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
MICROTUBULE NUCLEATION; MINUS-END; NEDD1; PHOSPHORYLATION; TARGETING FACTOR; PROTEIN NEDD1; RING COMPLEX; GCP-WD; CENTROSOME; ORGANIZATION; RECRUITMENT;
D O I
10.1083/jcb.201601099
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.-tubulin that are biochemically and functionally distinct and differentially regulated. Nucleation-competent CDK5RAP2-gamma-tubulin complexes were maintained at centrosomes upon initial epidermal differentiation. In contrast, Nedd1-gamma-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-gamma-tubulin complexes, providing a mechanistic link connecting MTOC activity and differentiation. Collectively, our studies demonstrate that distinct gamma-tubulin complexes regulate different microtubule behaviors at the centrosome and show that differential regulation of these complexes drives loss of centrosomal MTOC activity.
引用
收藏
页码:679 / 692
页数:14
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