Mechanical forces such as focused pressure or membrane stretch play central, but poorly understood, roles in biology. What types of molecules mediate mechanical signaling? Elegant electrophysiological studies have implicated a class of mechanically-gated ion channels in mechanotransduction. A recent breakthrough in this field is that analyses of C. elegans have identified members of a family of eukaryotic ion channels postulated to play central roles in mechanical signaling. In specialized touch sensory neurons, MEC-4 and MEC-10 channel subunits mediate touch transduction. A related subunit, UNC-8, modulates locomotion and is proposed to be involved in nematode proprioception (how an organism maintains a sense of where its different parts are and coordinates their motions). The identification of candidate mechanically-gated channels in C. elegans has now laid the groundwork for deciphering molecular mechanisms of mechanical signaling. Here the principal investigator proposes to combine genetic, molecular and biochemical approaches to deduce the molecular compositions and identify regulators of two mechanosensitive complexes. The specific goals are: 1) to test and extend models of channel/cytoskeleton interaction by defining protein interactions mediated by MEC-4 and MEC-10 intracellular domains; 2) to characterize the UNC-8 candidate proprioception channel by identification of subcellular localization, cellular site of action, and additional channel subunits; and 3) to clone and characterize 4 identified loci that genetically interact with unc-8 and to deduce the mechanisms by which they influence UNC-8 channel function. This work will test, refine and extend working models for molecular mechanisms of mechanotransduction, a significant issue because so little is understood of mechanical signaling and so many biological processes (ranging from cell volume regulation to the senses of touch, hearing and balance) depend upon it. In addition, the MEC-4/MEC-10 and UNC-8 channels are related to human ENaC channels that mediate Na+ readsorption and are essential for maintenance of electrolyte balance, blood pressure regulation, and clearing of fluid from neonatal lungs. Analyses of nematode and mammalian channels to date indicates that they work in fundamentally similar ways and thus data we generate in this work from a unique experimental perspective are expected to provide similar insight into general working of the channel class and hold implications for betterment of human health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS037955-01
Application #
2705245
Study Section
Neurology C Study Section (NEUC)
Program Officer
Leblanc, Gabrielle G
Project Start
1998-09-08
Project End
2002-08-31
Budget Start
1998-09-08
Budget End
1999-08-31
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Rutgers University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
038633251
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Wang, Ying; Apicella Jr, Alfonso; Lee, Sun-Kyung et al. (2008) A glial DEG/ENaC channel functions with neuronal channel DEG-1 to mediate specific sensory functions in C. elegans. EMBO J 27:2388-99
Bianchi, Laura; Driscoll, Monica (2006) Culture of embryonic C. elegans cells for electrophysiological and pharmacological analyses. WormBook :1-15
Royal, Dewey C; Bianchi, Laura; Royal, Mary Anne et al. (2005) Temperature-sensitive mutant of the Caenorhabditis elegans neurotoxic MEC-4(d) DEG/ENaC channel identifies a site required for trafficking or surface maintenance. J Biol Chem 280:41976-86
Bianchi, Laura; Gerstbrein, Beate; Frokjaer-Jensen, Christian et al. (2004) The neurotoxic MEC-4(d) DEG/ENaC sodium channel conducts calcium: implications for necrosis initiation. Nat Neurosci 7:1337-44
Bianchi, Laura; Kwok, Suk-Mei; Driscoll, Monica et al. (2003) A potassium channel-MiRP complex controls neurosensory function in Caenorhabditis elegans. J Biol Chem 278:12415-24
Tavernarakis, N; Everett, J K; Kyrpides, N C et al. (2001) Structural and functional features of the intracellular amino terminus of DEG/ENaC ion channels. Curr Biol 11:R205-8
Hong, K; Mano, I; Driscoll, M (2000) In vivo structure-function analyses of Caenorhabditis elegans MEC-4, a candidate mechanosensory ion channel subunit. J Neurosci 20:2575-88
Tavernarakis, N; Driscoll, M (2000) Caenorhabditis elegans degenerins and vertebrate ENaC ion channels contain an extracellular domain related to venom neurotoxins. J Neurogenet 13:257-64
Tavernarakis, N; Wang, S L; Dorovkov, M et al. (2000) Heritable and inducible genetic interference by double-stranded RNA encoded by transgenes. Nat Genet 24:180-3
Tavernarakis, N; Driscoll, M; Kyrpides, N C (1999) The SPFH domain: implicated in regulating targeted protein turnover in stomatins and other membrane-associated proteins. Trends Biochem Sci 24:425-7