ClC anion transport proteins are expressed in evolutionarily diverse organisms ranging from archaebacteria to mammals where they play essential roles in diverse processes such as systemic osmoregulation and regulation of cell and organelle Cl- and pH. Mutations in five of the nine human ClC genes give rise to or are associated with inherited muscle, bone, neurological and kidney disorders. Despite intensive study and their physiological importance, very little is known about how ClCs are regulated. We have exploited the genetic and molecular tractability of the nematode Caenorhabditis elegans to characterize the regulation and physiological roles of ClC channels that are assembled and operational in their native cellular environments. CLH-3b is a member of the mammalian ClC-1, 2, Ka and Kb anion channel subfamily, is expressed in the C. elegans oocyte and is activated by swelling and meiotic maturation via type 1 phosphatase mediated serine dephosphorylation. The Ste20 kinase GCK-3 binds to a 101 amino acid regulatory domain on the CLH-3b cytoplasmic C-terminus and functions to inhibit channel activity. Channel inhibition requires concomitant phosphorylation of two serine residues in the regulatory domain. Our studies of CLH-3b have provided the most detailed description of ClC channel regulation in the field. GCK-3 is a homolog of mammalian SPAK and OSR1. These kinases have emerged as critical regulators of diverse transport processes that play essential roles in cellular and systemic osmotic homeostasis. The SPAK/OSR1 signaling pathway is an important target for the development of new anti- hypertension drugs. We have shown that the role of GCK-3/SPAK/OSR1 signaling in osmosensing and systemic osmotic homeostasis is conserved from C. elegans to humans. The functional conservation of this signaling mechanism over hundreds of millions of years of evolution underscores its physiological significance. This renewal application builds on past successes of DK51610 and our unique understanding of CLH- 3b regulation to address two fundamental and unresolved questions: How do signaling events and conformational changes in the cytoplasmic C-terminus modulate and regulate ClC channel properties? How do cells and organisms detect osmotic perturbations and transduce those changes into specific responses? Our studies will use a variety of molecular, electrophysiological and biophysical approaches to characterize the signaling mechanisms by which GCK-3 and dephosphorylation control CLH-3b activity and to characterize conformational changes in the cytoplasmic C-terminus and outer pore that are induced by phosphorylation events. Detailed understanding of ClC biology is essential in order to fully define the role of these proteins in physiology and pathophysiology and their potential as therapeutic targets. Molecular understanding of cellular osmosensing represents a cornerstone for understanding and treating disturbances of salt and water balance that have a major impact on human health.

Public Health Relevance

ClC anion transport proteins carry out essential physiological functions and are associated with inherited muscle, bone, neurological and kidney disorders in humans. Studies described in this application will provide the first detailed description of how phosphorylation regulates ClC channel function and will provide new insights into mechanisms of cellular osmosensing. Detailed understanding of ClC regulation and cellular osmosensing is essential for understanding and treating disturbances of salt and water balance that have a major impact on human health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK051610-19
Application #
8286328
Study Section
Special Emphasis Panel (ZRG1-DKUS-A (02))
Program Officer
Ketchum, Christian J
Project Start
1996-09-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2014-06-30
Support Year
19
Fiscal Year
2012
Total Cost
$375,464
Indirect Cost
$164,054
Name
Mount Desert Island Biological Lab
Department
Type
DUNS #
077470003
City
Salsbury Cove
State
ME
Country
United States
Zip Code
04672
Yamada, Toshiki; Bhate, Manasi P; Strange, Kevin (2013) Regulatory phosphorylation induces extracellular conformational changes in a CLC anion channel. Biophys J 104:1893-904
Miyazaki, Hiroaki; Strange, Kevin (2012) Differential regulation of a CLC anion channel by SPAK kinase ortholog-mediated multisite phosphorylation. Am J Physiol Cell Physiol 302:C1702-12
Falin, Rebecca A; Miyazaki, Hiroaki; Strange, Kevin (2011) C. elegans STK39/SPAK ortholog-mediated inhibition of ClC anion channel activity is regulated by WNK-independent ERK kinase signaling. Am J Physiol Cell Physiol 300:C624-35
Strange, Kevin (2011) Putting the pieces together: a crystal clear window into CLC anion channel regulation. Channels (Austin) 5:101-5
Dave, Sonya; Sheehan, Jonathan H; Meiler, Jens et al. (2010) Unique gating properties of C. elegans ClC anion channel splice variants are determined by altered CBS domain conformation and the R-helix linker. Channels (Austin) 4:289-301
Falin, Rebecca A; Morrison, Rebecca; Ham, Amy-Joan L et al. (2009) Identification of regulatory phosphorylation sites in a cell volume- and Ste20 kinase-dependent ClC anion channel. J Gen Physiol 133:29-42
Strange, Kevin (2008) Authorship: why not just toss a coin? Am J Physiol Cell Physiol 295:C567-75
Strange, Kevin (2007) Revisiting the Krogh Principle in the post-genome era: Caenorhabditis elegans as a model system for integrative physiology research. J Exp Biol 210:1622-31
Strange, Kevin; Christensen, Michael; Morrison, Rebecca (2007) Primary culture of Caenorhabditis elegans developing embryo cells for electrophysiological, cell biological and molecular studies. Nat Protoc 2:1003-12
Choe, Keith P; Strange, Kevin (2007) Molecular and genetic characterization of osmosensing and signal transduction in the nematode Caenorhabditis elegans. FEBS J 274:5782-9

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