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J Biol Chem
2010 Nov 05;28545:34537-48. doi: 10.1074/jbc.M110.162545.
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Sorting motifs of the endosomal/lysosomal CLC chloride transporters.
Stauber T, Jentsch TJ.
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The CLC protein family contains plasma membrane chloride channels and the intracellular chloride-proton exchangers ClC-3-7. The latter proteins mainly reside on the various compartments of the endosomal-lysosomal system where they are involved in the luminal acidification or chloride accumulation. Although their partially overlapping subcellular distribution has been studied extensively, little is known about their targeting mechanism. In a comprehensive study we now performed pulldown experiments to systematically map the differential binding of adaptor proteins of the endosomal sorting machinery (adaptor proteins and GGAs (Golgi-localized, γ-ear containing, Arf binding)) as well as clathrin to the cytosolic regions of the intracellular CLCs. The resulting interaction pattern fitted well to the known subcellular localizations of the CLCs. By mutating potential sorting motifs, we could locate almost all binding sites, including one already known for ClC-3 and several new motifs for ClC-5, -6, and -7. The impact of the identified binding sites on the subcellular localization of CLC transporters was determined by heterologous expression of mutants. Surprisingly, some vesicular CLCs retained their localization after disruption of interaction sites. However, ClC-7 could be partially shifted from lysosomes to the plasma membrane by combined mutation of N-terminal sorting motifs. The localization of its β-subunit, Ostm1, was determined by that of ClC-7. Ostm1 was not capable of redirecting ClC-7 to lysosomes.
Bateman,
The structure of a domain common to archaebacteria and the homocystinuria disease protein.
1997, Pubmed
Bateman,
The structure of a domain common to archaebacteria and the homocystinuria disease protein.
1997,
Pubmed Bonifacino,
The GGA proteins: adaptors on the move.
2004,
Pubmed Bonifacino,
Signals for sorting of transmembrane proteins to endosomes and lysosomes.
2003,
Pubmed Brandt,
ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family.
1995,
Pubmed
,
Xenbase Braulke,
Sorting of lysosomal proteins.
2009,
Pubmed Cornejo,
Rapid recycling of ClC-2 chloride channels between plasma membrane and endosomes: role of a tyrosine endocytosis motif in surface retrieval.
2009,
Pubmed Dutzler,
X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity.
2002,
Pubmed Estévez,
Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion.
2001,
Pubmed
,
Xenbase Gentzsch,
The PDZ-binding chloride channel ClC-3B localizes to the Golgi and associates with cystic fibrosis transmembrane conductance regulator-interacting PDZ proteins.
2003,
Pubmed Günther,
ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells.
1998,
Pubmed Günther,
The ClC-5 chloride channel knock-out mouse - an animal model for Dent's disease.
2003,
Pubmed Hara-Chikuma,
ClC-3 chloride channels facilitate endosomal acidification and chloride accumulation.
2005,
Pubmed Hirst,
Spatial and functional relationship of GGAs and AP-1 in Drosophila and HeLa cells.
2009,
Pubmed Hryciw,
Nedd4-2 functionally interacts with ClC-5: involvement in constitutive albumin endocytosis in proximal tubule cells.
2004,
Pubmed
,
Xenbase Ignoul,
Human ClC-6 is a late endosomal glycoprotein that associates with detergent-resistant lipid domains.
2007,
Pubmed Jentsch,
Chloride and the endosomal-lysosomal pathway: emerging roles of CLC chloride transporters.
2007,
Pubmed Jentsch,
CLC chloride channels and transporters: from genes to protein structure, pathology and physiology.
2008,
Pubmed Jentsch,
Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes.
1990,
Pubmed
,
Xenbase Kasper,
Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration.
2005,
Pubmed Kornak,
Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man.
2001,
Pubmed Lange,
ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function.
2006,
Pubmed Li,
The ClC-3 chloride channel promotes acidification of lysosomes in CHO-K1 and Huh-7 cells.
2002,
Pubmed Lorenz,
Heteromultimeric CLC chloride channels with novel properties.
1996,
Pubmed
,
Xenbase Maritzen,
Role of the vesicular chloride transporter ClC-3 in neuroendocrine tissue.
2008,
Pubmed Miller,
Cytokine activation of nuclear factor kappa B in vascular smooth muscle cells requires signaling endosomes containing Nox1 and ClC-3.
2007,
Pubmed Mohammad-Panah,
The chloride channel ClC-4 contributes to endosomal acidification and trafficking.
2003,
Pubmed Mohammad-Panah,
The chloride channel ClC-4 co-localizes with cystic fibrosis transmembrane conductance regulator and may mediate chloride flux across the apical membrane of intestinal epithelia.
2002,
Pubmed Neagoe,
The late endosomal ClC-6 mediates proton/chloride countertransport in heterologous plasma membrane expression.
2010,
Pubmed
,
Xenbase Novarino,
Endosomal chloride-proton exchange rather than chloride conductance is crucial for renal endocytosis.
2010,
Pubmed Ogura,
ClC-3B, a novel ClC-3 splicing variant that interacts with EBP50 and facilitates expression of CFTR-regulated ORCC.
2002,
Pubmed Okkenhaug,
The human ClC-4 protein, a member of the CLC chloride channel/transporter family, is localized to the endoplasmic reticulum by its N-terminus.
2006,
Pubmed Peña-Münzenmayer,
Basolateral localization of native ClC-2 chloride channels in absorptive intestinal epithelial cells and basolateral sorting encoded by a CBS-2 domain di-leucine motif.
2005,
Pubmed Piccirillo,
An unconventional dileucine-based motif and a novel cytosolic motif are required for the lysosomal and melanosomal targeting of OA1.
2006,
Pubmed Poët,
Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6.
2006,
Pubmed Ponting,
CBS domains in CIC chloride channels implicated in myotonia and nephrolithiasis (kidney stones).
1997,
Pubmed Rickheit,
Role of ClC-5 in renal endocytosis is unique among ClC exchangers and does not require PY-motif-dependent ubiquitylation.
2010,
Pubmed Rickheit,
Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV.
2008,
Pubmed Robinson,
Adaptable adaptors for coated vesicles.
2004,
Pubmed Sakamoto,
Cellular and subcellular immunolocalization of ClC-5 channel in mouse kidney: colocalization with H+-ATPase.
1999,
Pubmed Salazar,
AP-3-dependent mechanisms control the targeting of a chloride channel (ClC-3) in neuronal and non-neuronal cells.
2004,
Pubmed Schwake,
An internalization signal in ClC-5, an endosomal Cl-channel mutated in dent's disease.
2001,
Pubmed
,
Xenbase Staub,
Regulation of stability and function of the epithelial Na+ channel (ENaC) by ubiquitination.
1997,
Pubmed
,
Xenbase Steinmeyer,
Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease.
1995,
Pubmed
,
Xenbase Stobrawa,
Disruption of ClC-3, a chloride channel expressed on synaptic vesicles, leads to a loss of the hippocampus.
2001,
Pubmed Suzuki,
Intracellular localization of ClC chloride channels and their ability to form hetero-oligomers.
2006,
Pubmed Vandewalle,
Tissue distribution and subcellular localization of the ClC-5 chloride channel in rat intestinal cells.
2001,
Pubmed Wang,
ClC-5: role in endocytosis in the proximal tubule.
2005,
Pubmed Wartosch,
Lysosomal degradation of endocytosed proteins depends on the chloride transport protein ClC-7.
2009,
Pubmed Weinert,
Lysosomal pathology and osteopetrosis upon loss of H+-driven lysosomal Cl- accumulation.
2010,
Pubmed Weinreich,
Pores formed by single subunits in mixed dimers of different CLC chloride channels.
2001,
Pubmed Weylandt,
ClC-3 expression enhances etoposide resistance by increasing acidification of the late endocytic compartment.
2007,
Pubmed Zerangue,
A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels.
1999,
Pubmed
,
Xenbase Zhao,
The ClC-3 chloride transport protein traffics through the plasma membrane via interaction of an N-terminal dileucine cluster with clathrin.
2007,
Pubmed