School of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QG, UK.
Proc Biol Sci. 2010 Jun 7;277(1688):1761-9. doi: 10.1098/rspb.2009.2355. Epub 2010 Feb 3.
The design principles and specific proteins of the dynein-tubulin motor, which powers the flagella and cilia of eukaryotes, have been conserved throughout the evolution of life from algae to humans. Cilia and flagella can support both motile and sensory functions independently, or sometimes in parallel to each other. In this paper we show that this dual sensory-motile role of eukaryotic cilia is preserved in the most sensitive of all invertebrate hearing organs, the Johnston's organ of the mosquito. The Johnston's organ displays spontaneous oscillations, which have been identified as being a characteristic of amplification in the ears of mosquitoes and Drosophila. In the auditory organs of Drosophila and vertebrates, the molecular basis of amplification has been attributed to the gating and adaptation of the mechanoelectrical transducer channels themselves. On the basis of their temperature-dependence and sensitivity to colchicine, we attribute the molecular basis of spontaneous oscillations by the Johnston's organ of the mosquito Culex quinquefasciatus, to the dynein-tubulin motor of the ciliated sensillae. If, as has been claimed for insect and vertebrate hearing organs, spontaneous oscillations epitomize amplification, then in the mosquito ear, this process is independent of mechanotransduction.
从藻类到人类,驱动真核生物鞭毛和纤毛的动力蛋白-微管的设计原理和特定蛋白质在生命进化过程中是保守的。纤毛和鞭毛可以独立地支持运动和感觉功能,或者有时可以彼此平行。在本文中,我们表明,真核纤毛的这种双重感觉-运动功能在所有无脊椎动物听觉器官中最敏感的蚊子的约翰斯顿器官中得到了保留。约翰斯顿器官显示自发振荡,这已被确定为蚊子和果蝇耳朵放大的特征。在果蝇和脊椎动物的听觉器官中,放大的分子基础归因于机械电换能通道本身的门控和适应。基于它们的温度依赖性和对秋水仙素的敏感性,我们将蚊子 Culex quinquefasciatus 的约翰斯顿器官的自发振荡的分子基础归因于纤毛感受器的动力蛋白-微管。如果像昆虫和脊椎动物听觉器官所声称的那样,自发振荡是放大的缩影,那么在蚊子的耳朵中,这个过程独立于机械转导。