Abstract
An apical tuft, which is observed in a wide range of embryos/larvae of marine invertebrates, is composed of a group of cilia that are longer and less motile than the abundant lateral cilia covering the rest of the embryonic surface. Although the apical tuft has been thought to function as a sensory organ, its molecular composition and roles are poorly understood. Here, we identified a glutathione transferase theta (GSTT) as an abundant and specific component of the apical tuft in sea urchin embryos. The expression of GSTT mRNA increases and becomes limited to the animal plate of the mesenchyme blastula, gastrula, and prism larva. Electron microscopy and tandem mass spectrometry demonstrated that the apical tuft contains almost every axonemal component for ciliary motility. Low concentrations of an inhibitor of glutathione transferase bromosulphophthalein (BSP) induce bending of apical tuft, suggesting that GSTT regulates motility of apical tuft cilia. Embryos treated with BSP swim with normal velocity and trajectories but show less efficiency of changing direction when they collide with an object. These results suggest that GSTT in the apical tuft plays an important role in the mechanical reception for the motility regulation of lateral motile cilia in sea urchin embryos.
Highlights
Cilia and flagella are microtubule-based structures that are well conserved among eukaryotes
We found that a glutathione transferase theta (GSTT; previously called glutathione S-transferase theta) is an abundant and specific component of apical tuft
As the apical tuft is located at the neurogenic animal plate in the sea urchin embryo, the cilia represent only a small number in each embryo
Summary
Cilia and flagella are microtubule-based structures that are well conserved among eukaryotes. The movement of these structures generates fluid flow for the locomotion. Motile cilia and flagella are centered by 912 microtubule structures called axonemes. The central apparatus is composed of radial spokes and central pair microtubules. These structures are thought to be involved in producing planar waveforms by regulating the dynein activity [reviewed in Gibbons, 1981; King, 2000; Porter and Sale, 2000; Mitchell, 2004; Smith and Yang, 2004; Inaba, 2003, 2007, 2011]
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