Asterless is a centriolar protein required for centrosome function and embryo development in Drosophila

被引:124
|
作者
Varmark, Hanne
Liamazares, Salud
Rebollo, Elena
Lange, Bodo
Reina, Jose
Schwarz, Heinz
Gonzalez, Cayetano
机构
[1] IRB Barcelona, Cell Div Grp, Barcelona 08028, Spain
[2] European Mol Biol Lab, Cell Biol & Biophys Programme, D-69117 Heidelberg, Germany
[3] Max Planck Inst Mol Genet, Dept Vertebrate Genom, D-14195 Berlin, Germany
[4] Max Planck Inst Dev Biol, Electron Microscopy Unit, D-72076 Tubingen, Germany
[5] ICREA, Passeig Lluis Co 23, Barcelona 08010, Spain
关键词
D O I
10.1016/j.cub.2007.09.031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Centrosomes, the major organizers of the microtubule network in most animal cells, are composed of centrioles embedded in a web of pericentriolar material (PCM). Recruitment and stabilization of PCM on the centrosome is a centriole-dependent function. Compared to the considerable number of PCM proteins known, the molecular characterization of centrioles is still very limited. Only a few centriolar proteins have been identified so far in Drosophila, most related to centriole duplication. Results: We have cloned asterless (aso and found that it encodes a 120 kD highly coiled-coil protein that is a constitutive pancentriolar and basal body component. Loss of asl function impedes the stabilization/maintenance of PCM at the centrosome. In embryos deficient for Asl, development is arrested right after fertilization. Asl shares significant homology with Cep152, a protein described as a component of the human centrosome for which no functional data is yet available. Conclusions: The cloning of asl offers new insight into the molecular composition of Drosophila centrioles and a possible model for the role of its human homolog. In addition, the phenotype of asl-deficient flies reveals that a functional centrosome is required for Drosophila embryo development.
引用
收藏
页码:1735 / 1745
页数:11
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