CLCN2 explained

Chloride channel protein 2 is a protein that in humans is encoded by the CLCN2 gene.[1] [2] Mutations of this gene have been found to cause leukoencephalopathy[3] and Idiopathic generalised epilepsy,[4] although the latter claim has been disputed.[5]

A gain of function mutation in the CLCN2 gene was found to cause primary aldosteronism,[6] a form of arterial hypertension due to excessive production of aldosterone by the neuroendocrine cells of the zona glomerulosa of the adrenal gland. The mutation was found to cause a chloride leak in these cells and increased the expression of aldosterone synthase.[7]

CLCN2 contains a transmembrane region that is involved in chloride ion transport as well two intracellular copies of the CBS domain.

See also

Further reading

Notes and References

  1. Cid LP, Montrose-Rafizadeh C, Smith DI, Guggino WB, Cutting GR . Cloning of a putative human voltage-gated chloride channel (CIC-2) cDNA widely expressed in human tissues . Human Molecular Genetics . 4 . 3 . 407–13 . March 1995 . 7795595 . 10.1093/hmg/4.3.407 .
  2. Web site: Entrez Gene: CLCN2 chloride channel 2.
  3. Depienne C, Bugiani M, Dupuits C, Galanaud D, Touitou V, Postma N, van Berkel C, Polder E, Tollard E, Darios F, Brice A, de Die-Smulders CE, Vles JS, Vanderver A, Uziel G, Yalcinkaya C, Frints SG, Kalscheuer VM, Klooster J, Kamermans M, Abbink TE, Wolf NI, Sedel F, van der Knaap MS . 6 . Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study . The Lancet. Neurology . 12 . 7 . 659–68 . July 2013 . 23707145 . 10.1016/S1474-4422(13)70053-X . free . 11858/00-001M-0000-0018-F3BD-9 . 16634353 .
  4. Combi R, Grioni D, Contri M, Redaelli S, Redaelli F, Bassi MT, Barisani D, Lavitrano ML, Tredici G, Tenchini ML, Bertolini M, Dalprà L . 6 . Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy . Brain Research Bulletin . 79 . 2 . 89–96 . April 2009 . 19200853 . 10.1016/j.brainresbull.2009.01.008 . 3036929 .
  5. Niemeyer MI, Cid LP, Sepúlveda FV, Blanz J, Auberson M, Jentsch TJ . No evidence for a role of CLCN2 variants in idiopathic generalized epilepsy . Nature Genetics . 42 . 1 . 3 . January 2010 . 20037607 . 10.1038/ng0110-3 . free .
  6. Fernandes-Rosa . Fabio L. . Daniil . Georgios . Orozco . Ian J. . Göppner . Corinna . El Zein . Rami . Jain . Vandana . Boulkroun . Sheerazed . Jeunemaitre . Xavier . Amar . Laurence . Lefebvre . Hervé . Schwarzmayr . Thomas . Strom . Tim M. . Jentsch . Thomas J. . Zennaro . Maria-Christina . March 2018 . A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism . Nature Genetics . en . 50 . 3 . 355–361 . 10.1038/s41588-018-0053-8 . 1546-1718.
  7. Stowasser . Michael . Wolley . Martin . Wu . Aihua . Gordon . Richard D. . Schewe . Julia . Stölting . Gabriel . Scholl . Ute I. . April 2019 . Pathogenesis of Familial Hyperaldosteronism Type II: New Concepts Involving Anion Channels . Current Hypertension Reports . en . 21 . 4 . 10.1007/s11906-019-0934-y . 1522-6417.