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A Novel zf-MYND Protein CHB-3 Mediates Guanylyl Cyclase Localization to Sensory Cilia and Controls Body Size of Caenorhabditis elegans

机译:新型zf-MYND蛋白CHB-3介导鸟苷酰环化酶定位到感觉纤毛并控制秀丽隐杆线虫的体型

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摘要

Cilia are important sensory organelles, which are thought to be essential regulators of numerous signaling pathways. In Caenorhabditis elegans, defects in sensory cilium formation result in a small-body phenotype, suggesting the role of sensory cilia in body size determination. Previous analyses suggest that lack of normal cilia causes the small-body phenotype through the activation of a signaling pathway which consists of the EGL-4 cGMP-dependent protein kinase and the GCY-12 receptor-type guanylyl cyclase. By genetic suppressor screening of the small-body phenotype of a cilium defective mutant, we identified a chb-3 gene. Genetic analyses placed chb-3 in the same pathway as egl-4 and gcy-12 and upstream of egl-4. chb-3 encodes a novel protein, with a zf-MYND motif and ankyrin repeats, that is highly conserved from worm to human. In chb-3 mutants, GCY-12 guanylyl cyclase visualized by tagged GFP (GCY-12::GFP) fails to localize to sensory cilia properly and accumulates in cell bodies. Our analyses suggest that decreased GCY-12 levels in the cilia of chb-3 mutants may cause the suppression of the small-body phenotype of a cilium defective mutant. By observing the transport of GCY-12::GFP particles along the dendrites to the cilia in sensory neurons, we found that the velocities and the frequencies of the particle movement are decreased in chb-3 mutant animals. How membrane proteins are trafficked to cilia has been the focus of extensive studies in vertebrates and invertebrates, although only a few of the relevant proteins have been identified. Our study defines a new regulator, CHB-3, in the trafficking process and also shows the importance of ciliary targeting of the signaling molecule, GCY-12, in sensory-dependent body size regulation in C. elegans. Given that CHB-3 is highly conserved in mammal, a similar system may be used in the trafficking of signaling proteins to the cilia of other species.
机译:纤毛是重要的感觉细胞器,被认为是许多信号通路的重要调节剂。在秀丽隐杆线虫中,感觉纤毛形成缺陷导致小体表型,提示感觉纤毛在体型确定中的作用。先前的分析表明,正常纤毛的缺乏会通过激活由EGL-​​4 cGMP依赖性蛋白激酶和GCY-12受体型鸟苷酸环化酶组成的信号通路而引起小体表型。通过遗传抑制子筛选纤毛缺陷突变体的小体表型,我们确定了一个chb-3基因。遗传分析将chb-3置于与egl-4和gcy-12相同的途径中,并位于egl-4的上游。 chb-3编码一种具有zf-MYND基序和锚蛋白重复序列​​的新型蛋白质,从蠕虫到人类都高度保守。在chb-3突变体中,通过标记的GFP(GCY-12 :: GFP)可视化的GCY-12鸟苷酸环化酶无法正确定位到感官纤毛并在细胞体内积聚。我们的分析表明,chb-3突变体纤毛中GCY-12水平降低可能会抑制纤毛缺陷突变体的小体表型。通过观察GCY-12 :: GFP颗粒沿着树突向感觉神经元纤毛的运输,我们发现chb-3突变动物的速度和运动频率降低。膜蛋白如何运输到纤毛一直是脊椎动物和无脊椎动物的广泛研究的焦点,尽管只有少数相关蛋白被鉴定出来。我们的研究在贩运过程中定义了一种新的调节剂CHB-3,并且还显示了纤毛靶向信号传导分子GCY-12在秀丽隐杆线虫的感官依赖性身体大小调节中的重要性。鉴于CHB-3在哺乳动物中高度保守,可以在将信号蛋白转运到其他物种的纤毛中使用类似的系统。

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