Yeo Hye Rim, Shin Mee Young, Kim Juri, Park Soon-Jung
Department of Tropical Medicine, Institute of Tropical Medicine, Yonsei University College of Medicine, Seoul 03722, Korea.
Parasites Hosts Dis. 2025 Feb;63(1):12-24. doi: 10.3347/PHD.24064. Epub 2025 Feb 25.
Intraflagellar transport (IFT) particles, a multi-protein apparatus composed of complex A and B, are known to be involved in homeostasis of flagella formation. IFT particles have recently become an interesting topic in Giardia lamblia, which has 4 pairs of flagella. In this experiment, we examined the function of giardial IFT components. When 7 components (IFT121, 140, 20, 46, 52, 81, and 88) of IFT were expressed in Giardia trophozoites as a tagged form with mNeonGreen, all of them were found in both flagella pores and cytoplasmic axonemes. In addition, motor proteins for IFT particles (kinesin-13 and kinesin-2b), were localized to a median body and cytoplasmic flagella, respectively. The CRISPRi-mediated knockdown of IFT88 significantly affected the lengths of all 4 flagella compared to the control cells, Giardia expressing dead Cas9 using control guide RNA. Decreased expression of kinesin-2b also resulted in shortening of flagella, excluding the ventral flagella. Live Giardia cells expressing IFT88-mNeonGreen clearly demonstrated fluorescence in flagella pores and cytoplasmic axonemes. These results on IFT88 and kinesin-2b indicate that IFT complex plays a role in maintenance of G. lamblia flagella.
鞭毛内运输(IFT)颗粒是一种由A复合体和B复合体组成的多蛋白装置,已知其参与鞭毛形成的稳态。IFT颗粒最近在拥有4对鞭毛的蓝氏贾第鞭毛虫中成为一个有趣的研究课题。在本实验中,我们研究了贾第鞭毛虫IFT组分的功能。当IFT的7种组分(IFT121、140、20、46、52、81和88)以与mNeonGreen融合的标记形式在贾第鞭毛虫滋养体中表达时,它们均在鞭毛孔和细胞质轴丝中被发现。此外,IFT颗粒的驱动蛋白(驱动蛋白-13和驱动蛋白-2b)分别定位于中体和细胞质鞭毛。与使用对照向导RNA表达无活性Cas9的对照细胞(贾第鞭毛虫)相比,CRISPRi介导的IFT88敲低显著影响了所有4根鞭毛的长度。驱动蛋白-2b表达的降低也导致鞭毛缩短,但腹侧鞭毛除外。表达IFT88-mNeonGreen的活贾第鞭毛虫细胞在鞭毛孔和细胞质轴丝中清晰地显示出荧光。这些关于IFT88和驱动蛋白-2b的结果表明,IFT复合体在维持蓝氏贾第鞭毛虫鞭毛方面发挥作用。