Ciliary transition zone activation of phosphorylated Tctex-1 controls ciliary resorption, S-phase entry and fate of neural progenitors

被引:183
作者
Li, Aiqun [1 ]
Saito, Masaki [1 ,2 ,3 ]
Chuang, Jen-Zen [1 ]
Tseng, Yun-Yu [1 ]
Dedesma, Carlos [1 ]
Tomizawa, Kazuhito [4 ]
Kaitsuka, Taku [4 ]
Sung, Ching-Hwa [1 ,5 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Ophthalmol, Margaret M Dyson Vis Res Inst, New York, NY 10065 USA
[2] Tohoku Univ, Inst Int Adv Interdisciplinary Res, Int Adv Res & Educ Org, Aoba Ku, Sendai, Miyagi 9808578, Japan
[3] Tohoku Univ, Dept Cellular Signalling, Grad Sch Pharmaceut Sci, Aoba Ku, Sendai, Miyagi 9808578, Japan
[4] Kumamoto Univ, Fac Life Sci, Dept Mol Physiol, Kumamoto 8608556, Japan
[5] Cornell Univ, Weill Med Coll, Dept Cell & Dev Biol, New York, NY 10065 USA
关键词
DYNEIN LIGHT-CHAIN; CELL-CYCLE CONTROL; CYTOPLASMIC DYNEIN; PRIMARY CILIUM; STEM-CELLS; MAMMALIAN NEUROGENESIS; NEURONAL MIGRATION; PLANAR DIVISIONS; PROTEIN; BRAIN;
D O I
10.1038/ncb2218
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Primary cilia are displayed during the G(0)/G(1) phase of many cell types. Cilia are resorbed as cells prepare to re-enter the cell cycle, but the causal and molecular link between these two cellular events remains unclear. We show that Tctex-1 phosphorylated at Thr 94 is recruited to ciliary transition zones before S-phase entry and has a pivotal role in both ciliary disassembly and cell cycle progression. However, the role of Tctex-1 in S-phase entry is dispensable in non-ciliated cells. Exogenously adding a phosphomimic Tctex-1(T94E) mutant accelerates cilium disassembly and S-phase entry. These results support a model in which the cilia act as a brake to prevent cell cycle progression. Mechanistic studies show the involvement of actin dynamics in Tctex-1-regulated cilium resorption. Tctex-1 phosphorylated at Thr 94 is also selectively enriched at the ciliary transition zones of cortical neural progenitors, and has a key role in controlling G(1) length, cell cycle entry and fate determination of these cells during corticogenesis.
引用
收藏
页码:402 / U142
页数:18
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