Abstract

Mechanotransduction in Caenorhabditis elegans touch receptor neurons is mediated by an ion channel formed by MEC-4, MEC-10, and accessory proteins. To define the role of these subunits in the channel's response to mechanical force, we expressed degenerin channels comprising MEC-4 and MEC-10 in Xenopus oocytes and examined their response to laminar shear stress (LSS). Shear stress evoked a rapid increase in whole cell currents in oocytes expressing degenerin channels as well as channels with a MEC-4 degenerin mutation (MEC-4d), suggesting that C. elegans degenerin channels are sensitive to LSS. MEC-10 is required for a robust LSS response as the response was largely blunted in oocytes expressing homomeric MEC-4 or MEC-4d channels. We examined a series of MEC-10/MEC-4 chimeras to identify specific domains (amino terminus, first transmembrane domain, and extracellular domain) and sites (residues 130-132 and 134-137) within MEC-10 that are required for a robust response to shear stress. In addition, the LSS response was largely abolished by MEC-10 mutations encoded by a touch-insensitive mec-10 allele, providing a correlation between the channel's responses to two different mechanical forces. Our findings suggest that MEC-10 has an important role in the channel's response to mechanical forces.

Highlights

  • 14012 JOURNAL OF BIOLOGICAL CHEMISTRY meable to Naϩ and Ca2ϩ [8, 9] and sensitive to amiloride and specific amiloride derivatives [10]

  • The C. elegans Degenerin Channel Is Activated by Shear Stress—To examine whether C. elegans degenerin channels respond to laminar shear stress (LSS), we used a perfusion system in which vertical fluid flow is delivered via a pipette placed in close proximity to the Xenopus oocyte surface to apply shear stress [24, 26]

  • MEC-4 and MEC-10 were co-expressed with an accessory protein (MEC-2) and a chaperone (MEC-6) as amiloride-sensitive Naϩ currents in oocytes expressing MEC-4 alone or MEC-4/ MEC-10 were significantly enhanced by co-expressing MEC-2 and MEC-6 [8, 27, 28]

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Summary

Experimental Procedures

Domain Swap and Site-directed Mutagenesis—MEC-4 in the pGEM-HE vector and MEC-10 in the pSGEM vector were used as templates to generate five MEC-10/4 chimeras shown in Fig. 1: 1) MEC-10-4NTM1 in which the N terminus and the first transmembrane domain (TM1) of MEC-10 (residues Met1– Tyr146) were replaced with the corresponding MEC-4 region (residues Met1–Tyr133), 2) MEC-10-4N in which the N termi-

LSS Activates Worm Degenerin Channel
Results
NSc ϩ
Discussion

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