Proceedings of the National Academy of Sciences of the United States of America · 2014
Conserved TCP domain of Sas-4/CPAP is essential for pericentriolar material tethering during centrosome biogenesis.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Zheng Xiangdong, Gooi Li Ming, Wason Arpit, Gabriel Elke, Mehrjardi Narges Zare, Yang Qian, Zhang Xingrun, Debec Alain, Basiri Marcus L, Avidor-Reiss Tomer, Pozniakovsky Andrei, Poser Ina, Saric Tomo, Hyman Anthony A, Li Haitao, Gopalakrishnan Jay
Аннотация
Pericentriolar material (PCM) recruitment to centrioles forms a key step in centrosome biogenesis. Deregulation of this process leads to centrosome aberrations causing disorders, one of which is autosomal recessive primary microcephaly (MCPH), a neurodevelopmental disorder where brain size is reduced. During PCM recruitment, the conserved centrosomal protein Sas-4/CPAP/MCPH6, known to play a role in centriole formation, acts as a scaffold for cytoplasmic PCM complexes to bind and then tethers them to centrioles to form functional centrosomes. To understand Sas-4's tethering role, we determined the crystal structure of its T complex protein 10 (TCP) domain displaying a solvent-exposed single-layer of β-sheets fold. This unique feature of the TCP domain suggests that it could provide an "extended surface-like" platform to tether the Sas-4-PCM scaffold to a centriole. Functional studies in Drosophila, human cells, and human induced pluripotent stem cell-derived neural progenitor cells were used to test this hypothesis, where point mutations within the 9-10th β-strands (β9-10 mutants including a MCPH-associated mutation) perturbed PCM tethering while allowing Sas-4/CPAP to scaffold cytoplasmic PCM complexes. Specifically, the Sas-4 β9-10 mutants displayed perturbed interactions with Ana2, a centrosome duplication factor, and Bld-10, a centriole microtubule-binding protein, suggesting a role for the β9-10 surface in mediating protein-protein interactions for efficient Sas-4-PCM scaffold centriole tethering. Hence, we provide possible insights into how centrosomal protein defects result in human MCPH and how Sas-4 proteins act as a vehicle to tether PCM complexes to centrioles independent of its well-known role in centriole duplication.
Предметные рубрики MeSH
AnimalsAnimals, Genetically ModifiedBrainCentriolesCentrosomeCytoplasmDrosophila ProteinsDrosophila melanogasterHumansInduced Pluripotent Stem CellsMaleMicrocephalyMicrotubule-Associated ProteinsModels, MolecularPoint MutationProtein BindingProtein Structure, SecondaryProtein Structure, TertiaryTestis