The centrosomal component CEP161 of Dictyostelium discoideum interacts with the Hippo signaling pathway

被引:8
作者
Sukumaran, Salil K. [1 ,2 ,3 ]
Blau-Wasser, Rosemarie [1 ,2 ,3 ]
Rohlfs, Meino [4 ]
Gallinger, Christoph [4 ]
Schleicher, Michael [4 ]
Noegel, Angelika A. [1 ,2 ,3 ]
机构
[1] Univ Cologne, Fac Med, Inst Biochem 1, D-50931 Cologne, Germany
[2] Univ Cologne, CMMC, D-50931 Cologne, Germany
[3] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany
[4] Univ Munich, Inst Anat & Cell Biol, Munich, Germany
关键词
CEP161; centrosome; Dictyostelium discoideum; hippo kinase; Hippo signaling; SITE-A GLYCOPROTEIN; CELL-CYCLE EXIT; PROLIFERATION ARREST; PROMOTES APOPTOSIS; DROSOPHILA; KINASE; GROWTH; HOMOLOG; PROTEINS; PHAGOCYTOSIS;
D O I
10.1080/15384101.2015.1007015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CEP161 is a novel component of the Dictyostelium discoideum centrosome which was identified as binding partner of the pericentriolar component CP250. Here we show that the amino acids 1-763 of the 1381 amino acids CEP161 are sufficient for CP250 binding, centrosomal targeting and centrosome association. Analysis of AX2 cells over-expressing truncated and full length CEP161 proteins revealed defects in growth and development. By immunoprecipitation experiments we identified the Hippo related kinase SvkA (Hrk-svk) as binding partner for CEP161. Both proteins colocalize at the centrosome. In in vitro kinase assays the N-terminal domain of CEP161 (residues 1-763) inhibited the kinase activity of Hrk-svk. A comparison of D. discoideum Hippo kinase mutants with mutants overexpressing CEP161 polypeptides revealed similar defects. We propose that the centrosomal component CEP161 is a novel player in the Hippo signaling pathway and affects various cellular properties through this interaction.
引用
收藏
页码:1024 / 1035
页数:12
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