Literature DB >> 23983121

Common gating of both CLC transporter subunits underlies voltage-dependent activation of the 2Cl-/1H+ exchanger ClC-7/Ostm1.

Carmen F Ludwig1, Florian Ullrich, Lilia Leisle, Tobias Stauber, Thomas J Jentsch.   

Abstract

CLC anion transporters form dimers that function either as Cl(-) channels or as electrogenic Cl(-)/H(+) exchangers. CLC channels display two different types of "gates," "protopore" gates that open and close the two pores of a CLC dimer independently of each other and common gates that act on both pores simultaneously. ClC-7/Ostm1 is a lysosomal 2Cl(-)/1H(+) exchanger that is slowly activated by depolarization. This gating process is drastically accelerated by many CLCN7 mutations underlying human osteopetrosis. Making use of some of these mutants, we now investigate whether slow voltage activation of plasma membrane-targeted ClC-7/Ostm1 involves protopore or common gates. Voltage activation of wild-type ClC-7 subunits was accelerated by co-expressing an excess of ClC-7 subunits carrying an accelerating mutation together with a point mutation rendering these subunits transport-deficient. Conversely, voltage activation of a fast ClC-7 mutant could be slowed by co-expressing an excess of a transport-deficient mutant. These effects did not depend on whether the accelerating mutation localized to the transmembrane part or to cytoplasmic cystathionine-β-synthase (CBS) domains of ClC-7. Combining accelerating mutations in the same subunit did not speed up gating further. No currents were observed when ClC-7 was truncated after the last intramembrane helix. Currents and slow gating were restored when the C terminus was co-expressed by itself or fused to the C terminus of the β-subunit Ostm1. We conclude that common gating underlies the slow voltage activation of ClC-7. It depends on the CBS domain-containing C terminus that does not require covalent binding to the membrane domain of ClC-7.

Entities:  

Keywords:  Albers-Schönberg Disease; Anion Transport; Antiport; Chloride Transport; Gating; Ion Channels; Lysosomal Storage Disease; Split-channel

Mesh:

Substances:

Year:  2013        PMID: 23983121      PMCID: PMC3789960          DOI: 10.1074/jbc.M113.509364

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  59 in total

1.  X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity.

Authors:  Raimund Dutzler; Ernest B Campbell; Martine Cadene; Brian T Chait; Roderick MacKinnon
Journal:  Nature       Date:  2002-01-17       Impact factor: 49.962

2.  Lysosomal pathology and osteopetrosis upon loss of H+-driven lysosomal Cl- accumulation.

Authors:  Stefanie Weinert; Sabrina Jabs; Chayarop Supanchart; Michaela Schweizer; Niclas Gimber; Martin Richter; Jörg Rademann; Tobias Stauber; Uwe Kornak; Thomas J Jentsch
Journal:  Science       Date:  2010-06-11       Impact factor: 47.728

3.  Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human.

Authors:  Nader Chalhoub; Nadia Benachenhou; Venkatesh Rajapurohitam; Monica Pata; Mathieu Ferron; Annalisa Frattini; Anna Villa; Jean Vacher
Journal:  Nat Med       Date:  2003-03-10       Impact factor: 53.440

4.  Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man.

Authors:  U Kornak; D Kasper; M R Bösl; E Kaiser; M Schweizer; A Schulz; W Friedrich; G Delling; T J Jentsch
Journal:  Cell       Date:  2001-01-26       Impact factor: 41.582

5.  Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.

Authors:  E Cleiren; O Bénichou; E Van Hul; J Gram; J Bollerslev; F R Singer; K Beaverson; A Aledo; M P Whyte; T Yoneyama; M C deVernejoul; W Van Hul
Journal:  Hum Mol Genet       Date:  2001-12-01       Impact factor: 6.150

6.  Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion.

Authors:  R Estévez; T Boettger; V Stein; R Birkenhäger; E Otto; F Hildebrandt; T J Jentsch
Journal:  Nature       Date:  2001-11-29       Impact factor: 49.962

7.  Biophysical properties of ClC-3 differentiate it from swelling-activated chloride channels in Chinese hamster ovary-K1 cells.

Authors:  X Li; K Shimada; L A Showalter; S A Weinman
Journal:  J Biol Chem       Date:  2000-11-17       Impact factor: 5.157

8.  Different fast-gate regulation by external Cl(-) and H(+) of the muscle-type ClC chloride channels.

Authors:  M F Chen; T Y Chen
Journal:  J Gen Physiol       Date:  2001-07       Impact factor: 4.086

9.  Pores formed by single subunits in mixed dimers of different CLC chloride channels.

Authors:  F Weinreich; T J Jentsch
Journal:  J Biol Chem       Date:  2000-10-16       Impact factor: 5.157

10.  Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel.

Authors:  M Pusch; K Steinmeyer; M C Koch; T J Jentsch
Journal:  Neuron       Date:  1995-12       Impact factor: 17.173

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  22 in total

Review 1.  A tale of two CLCs: biophysical insights toward understanding ClC-5 and ClC-7 function in endosomes and lysosomes.

Authors:  Giovanni Zifarelli
Journal:  J Physiol       Date:  2015-06-26       Impact factor: 5.182

Review 2.  Structure and gating of CLC channels and exchangers.

Authors:  Alessio Accardi
Journal:  J Physiol       Date:  2015-07-28       Impact factor: 5.182

Review 3.  Discovery of CLC transport proteins: cloning, structure, function and pathophysiology.

Authors:  Thomas J Jentsch
Journal:  J Physiol       Date:  2015-08-24       Impact factor: 5.182

4.  Regulatory Conformational Coupling between CLC Anion Channel Membrane and Cytoplasmic Domains.

Authors:  Toshiki Yamada; Kevin Strange
Journal:  Biophys J       Date:  2016-11-01       Impact factor: 4.033

5.  Tonic inhibition of the chloride/proton antiporter ClC-7 by PI(3,5)P2 is crucial for lysosomal pH maintenance.

Authors:  Xavier Leray; Jacob K Hilton; Kamsi Nwangwu; Alissa Becerril; Vedrana Mikusevic; Gabriel Fitzgerald; Anowarul Amin; Mary R Weston; Joseph A Mindell
Journal:  Elife       Date:  2022-06-07       Impact factor: 8.713

6.  A Recurrent Gain-of-Function Mutation in CLCN6, Encoding the ClC-6 Cl-/H+-Exchanger, Causes Early-Onset Neurodegeneration.

Authors:  Maya M Polovitskaya; Carlo Barbini; Diego Martinelli; Frederike L Harms; F Sessions Cole; Paolo Calligari; Gianfranco Bocchinfuso; Lorenzo Stella; Andrea Ciolfi; Marcello Niceta; Teresa Rizza; Marwan Shinawi; Kathleen Sisco; Jessika Johannsen; Jonas Denecke; Rosalba Carrozzo; Daniel J Wegner; Kerstin Kutsche; Marco Tartaglia; Thomas J Jentsch
Journal:  Am J Hum Genet       Date:  2020-11-19       Impact factor: 11.025

Review 7.  Genetics of Osteopetrosis.

Authors:  Eleonora Palagano; Ciro Menale; Cristina Sobacchi; Anna Villa
Journal:  Curr Osteoporos Rep       Date:  2018-02       Impact factor: 5.096

8.  Transport activity and presence of ClC-7/Ostm1 complex account for different cellular functions.

Authors:  Stefanie Weinert; Sabrina Jabs; Svea Hohensee; Wing Lee Chan; Uwe Kornak; Thomas J Jentsch
Journal:  EMBO Rep       Date:  2014-05-12       Impact factor: 8.807

9.  Clcn7F318L/+ as a new mouse model of Albers-Schönberg disease.

Authors:  J Caetano-Lopes; S G Lessard; S Hann; K Espinoza; K S Kang; K E Lim; D J Horan; H R Noonan; D Hu; R Baron; A G Robling; M L Warman
Journal:  Bone       Date:  2017-09-20       Impact factor: 4.626

10.  Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders.

Authors:  Anna R Duncan; Maya M Polovitskaya; Héctor Gaitán-Peñas; Sara Bertelli; Grace E VanNoy; Patricia E Grant; Anne O'Donnell-Luria; Zaheer Valivullah; Alysia Kern Lovgren; Elaina M England; Emanuele Agolini; Jill A Madden; Klaus Schmitz-Abe; Amy Kritzer; Pamela Hawley; Antonio Novelli; Paolo Alfieri; Giovanna Stefania Colafati; Dagmar Wieczorek; Konrad Platzer; Johannes Luppe; Margarete Koch-Hogrebe; Rami Abou Jamra; Juanita Neira-Fresneda; Anna Lehman; Cornelius F Boerkoel; Kimberly Seath; Lorne Clarke; Yvette van Ierland; Emanuela Argilli; Elliott H Sherr; Andrea Maiorana; Thilo Diel; Maja Hempel; Tatjana Bierhals; Raúl Estévez; Thomas J Jentsch; Michael Pusch; Pankaj B Agrawal
Journal:  Am J Hum Genet       Date:  2021-06-28       Impact factor: 11.043

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