共 46 条
Building a centriole
被引:61
作者:

Avidor-Reiss, Tomer
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h-index: 0
机构:
Univ Toledo, Dept Biol Sci, Toledo, OH 43606 USA Univ Toledo, Dept Biol Sci, Toledo, OH 43606 USA

Gopalakrishnan, Jayachandran
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h-index: 0
机构:
Univ Cologne, Ctr Mol Med, Cologne, Germany
Univ Cologne, Inst Biochem 1, Cologne, Germany Univ Toledo, Dept Biol Sci, Toledo, OH 43606 USA
机构:
[1] Univ Toledo, Dept Biol Sci, Toledo, OH 43606 USA
[2] Univ Cologne, Ctr Mol Med, Cologne, Germany
[3] Univ Cologne, Inst Biochem 1, Cologne, Germany
基金:
美国国家科学基金会;
关键词:
CENTROSOME DUPLICATION;
9-FOLD SYMMETRY;
BASAL BODY;
C-ELEGANS;
PROTEIN;
CPAP;
PLK4;
INTERACTS;
SCAFFOLD;
CEP152;
D O I:
10.1016/j.ceb.2012.10.016
中图分类号:
Q2 [细胞生物学];
学科分类号:
071013 [干细胞生物学];
摘要:
Centrioles are the key foundation of centrosomes and cilia, yet a molecular understanding of how they form has only recently begun to emerge. Building a fully functional centriole that can form a centrosome and cilium requires two cell cycles. Centriole building starts with procentriole nucleation, a process that is coordinated by the conserved proteins Plk4/Zyg-1, and Asterless/Cep1 52. Subsequently, Sas-6, a conserved procentriole protein, self-assembles to provide nine-fold symmetry to the centriole scaffold. The procentriole then continues to elongate into a centriole, a process controlled by Sas-4/CPAP and CP110. Then, centrioles recruit Sas-4-mediated pre-assembled centrosomal complexes from the cytoplasm to form the pericentriolar material (PCM). Finally, CP110 and its interacting proteins are involved in controlling the timing of centriole templating of the cilium.
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页码:72 / 77
页数:6
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