Meng Dan, Pan Junmin
MOE Key Laboratory of Protein Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.
MOE Key Laboratory of Protein Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China MOE Key Laboratory of Protein Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China MOE Key Laboratory of Protein Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Mol Biol Cell. 2016 Mar 1;27(5):838-47. doi: 10.1091/mbc.E15-10-0707. Epub 2016 Jan 13.
NIMA-related kinases (Nrks or Neks) have emerged as key regulators of ciliogenesis. In human, mutations in Nek1 and Nek8 cause cilia-related disorders. The ciliary functions of Nrks are mostly revealed by genetic studies; however, the underlying mechanisms are not well understood. Here we show that a Chlamydomonas Nrk, CNK4, regulates ciliary stability and length. CNK4 is localized to the basal body region and the flagella. The cnk4-null mutant exhibited long flagella, with formation of flagellar bulges. The flagella gradually became curled at the bulge formation site, leading to flagellar loss. Electron microscopy shows that the curled flagella involved curling and degeneration of axonemal microtubules. cnk4 mutation resulted in flagellar increases of IFT trains, as well as its accumulation at the flagellar bulges. IFT speeds were not affected, however, IFT trains frequently stalled, leading to reduced IFT frequencies. These data are consistent with a model in which CNK4 regulates microtubule dynamics and IFT to control flagellar stability and length.
NIMA相关激酶(Nrks或Neks)已成为纤毛发生的关键调节因子。在人类中,Nek1和Nek8的突变会导致与纤毛相关的疾病。Nrks的纤毛功能大多通过遗传学研究揭示;然而,其潜在机制尚不清楚。在这里,我们表明衣藻Nrk,即CNK4,调节纤毛的稳定性和长度。CNK4定位于基体区域和鞭毛。cnk4基因缺失突变体表现出长鞭毛,并形成鞭毛凸起。鞭毛在凸起形成部位逐渐卷曲,导致鞭毛丢失。电子显微镜显示,卷曲的鞭毛涉及轴丝微管的卷曲和退化。cnk4突变导致鞭毛中IFT列车增加,以及其在鞭毛凸起处的积累。IFT速度不受影响,然而,IFT列车经常停滞,导致IFT频率降低。这些数据与一个模型一致,即CNK4调节微管动力学和IFT以控制鞭毛的稳定性和长度。