Department of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, NRB-0939, Boston, MA 02115, USA.
J Am Soc Nephrol. 2011 May;22(5):832-7. doi: 10.1681/ASN.2010090992. Epub 2011 Apr 7.
Polycystic kidney disease (PKD) in mice can arise from defects in Nek kinases, which participate in ciliogenesis. PKD can also arise from loss of the protein TAZ, an adaptor protein in the E3 ubiquitin ligase complex that targets the ciliary protein polycystin 2 (PC2) for degradation, but whether Nek and TAZ contribute to the same biochemical pathway is unknown. Here, we report that the nimA-related protein kinase Nek1 phosphorylates TAZ at a site essential for the ubiquitination and proteasomal degradation of PC2. Loss of Nek1 leads to underphosphorylation of TAZ, thereby promoting the abnormal accumulation of PC2. Furthermore, TAZ targets Nek1 for degradation. These data suggest that TAZ and Nek1 constitute a negative feedback loop linked through phosphorylation and ubiquitination and that the interaction of Nek1 and TAZ maintain PC2 at the level needed for proper ciliogenesis.
多囊肾病 (PKD) 在小鼠中可以由 Nek 激酶的缺陷引起,Nek 激酶参与纤毛发生。PKD 也可能由于 E3 泛素连接酶复合物中的衔接蛋白 TAZ 的缺失而发生,TAZ 是靶向纤毛蛋白多囊蛋白 2 (PC2) 进行降解的 E3 泛素连接酶复合物中的衔接蛋白,但 Nek 和 TAZ 是否参与相同的生化途径尚不清楚。在这里,我们报告说,与 nimA 相关的蛋白激酶 Nek1 在 PC2 的泛素化和蛋白酶体降解所必需的位点上磷酸化 TAZ。Nek1 的缺失导致 TAZ 的低磷酸化,从而促进 PC2 的异常积累。此外,TAZ 将 Nek1 靶向降解。这些数据表明,TAZ 和 Nek1 构成一个负反馈回路,通过磷酸化和泛素化连接,Nek1 和 TAZ 的相互作用将 PC2 维持在适当的纤毛发生所需的水平。