Ankyrin-3 Explained

Ankyrin-3 (ANK-3), also known as ankyrin-G, is a protein from ankyrin family that in humans is encoded by the ANK3 gene.[1] [2]

Function

The protein encoded by this gene, ankyrin-3 is an immunologically distinct gene product from ankyrins ANK1 and ANK2, and was originally found at the axonal initial segment and nodes of Ranvier of neurons in the central and peripheral nervous systems. Alternatively spliced variants may be expressed in other tissues. Although multiple transcript variants encoding several different isoforms have been found for this gene, the full-length nature of only two have been characterized.[1]

Within the nervous system, ankyrin-G is specifically localized to the neuromuscular junction, the axon initial segment and the Nodes of Ranvier.[3] Within the nodes of Ranvier where action potentials are actively propagated, ankyrin-G has long been thought to be the intermediate binding partner to neurofascin and voltage-gated sodium channels.[4] The genetic deletion of ankyrin-G from multiple neuron types has shown that ankyrin-G is required for the normal clustering of voltage-gated sodium channels at the axon hillock and for action potential firing.[5] [6]

Disease linkage

The ANK3 protein associates with the cardiac sodium channel Nav1.5 . Both proteins are highly expressed at ventricular intercalated disc and T-tubule membranes in cardiomyocytes. A mutation in the Nav1.5 protein blocks interaction with ANK3 binding and therefore disrupts surface expression of Nav1.5 in cardiomyocytes resulting in Brugada syndrome, a type of cardiac arrhythmia.[7]

Other mutations in the ANK3 gene may be involved in the bipolar disorder and intellectual disability.[8] [9] [10] [11]

Ankyrin family

The protein encoded by the ANK3 gene is a member of the ankyrin family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton. Ankyrins play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation.[1]

Further reading

Notes and References

  1. Web site: Entrez Gene: ANK2 ankyrin 3, node of Ranvier .
  2. Kapfhamer D, Miller DE, Lambert S, Bennett V, Glover TW, Burmeister M . Chromosomal localization of the ankyrin-G gene (ANK3/Ank3) to human 10q21 and mouse 10 . Genomics . 27 . 1 . 189–91 . May 1995 . 7665168 . 10.1006/geno.1995.1023 .
  3. Lambert S, Davis JQ, Bennett V . Morphogenesis of the node of Ranvier: co-clusters of ankyrin and ankyrin-binding integral proteins define early developmental intermediates. . J. Neurosci. . 17 . 18 . 7025–36 . September 1997 . 9278538 . 10.1523/JNEUROSCI.17-18-07025.1997. free . 6573274 .
  4. Srinivasan Y, Lewallen M, Angelides KJ . Mapping the binding site on ankyrin for the voltage-dependent sodium channel from brain. . J Biol Chem . 267 . 11 . 7483–9 . April 1992 . 10.1016/S0021-9258(18)42543-4 . 1313804 . free .
  5. Zhou D, Lambert S, Malen PL, Carpenter S, Boland LM, Bennett V . AnkyrinG Is Required for Clustering of Voltage-gated Na Channels at Axon Initial Segments and for Normal Action Potential Firing . J. Cell Biol. . 143 . 5 . 1295–1304 . November 1998 . 9832557 . 10.1083/jcb.143.5.1295. 2133082.
  6. Hedstrom KL, Xu X, Ogawa Y, Frischknecht R, Seidenbecher CI, Shrager P, Rasband MN . Neurofascin assembles a specialized extracellular matrix at the axon initial segment . J. Cell Biol. . 178 . 5 . 875–886 . August 2007 . 17709431 . 10.1083/jcb.200705119. 2064550.
  7. Mohler PJ, Rivolta I, Napolitano C, LeMaillet G, Lambert S, Priori SG, Bennett V . Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes . Proc. Natl. Acad. Sci. U.S.A. . 101 . 50 . 17533–8 . December 2004 . 15579534 . 536011 . 10.1073/pnas.0403711101 . 2004PNAS..10117533M . free .
  8. Web site: Bipolar Disorder Discovery at the Nano Level . 2014-12-01 . dead . https://web.archive.org/web/20141204063840/http://www.yumanewsnow.com/index.php/news/health/8847-bipolar-disorder-discovery-at-the-nano-level . 2014-12-04 .
  9. Ferreira MA . Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder . Nat. Genet. . 40. 9. 1056–8. August 2008 . 18711365 . 10.1038/ng.209 . 2703780 . vanc . O'Donovan MC . Meng YA . 3 . Jones . Ian R . Ruderfer . Douglas M . Jones . Lisa . Fan . Jinbo . Kirov . George . Perlis . Roy H .
  10. Web site: Channeling Mental Illness: GWAS Links Ion Channels, Bipolar Disorder . https://web.archive.org/web/20101218195754/http://schizophreniaforum.org/new/detail.asp?id=1450 . dead . 2010-12-18 . 2008-08-19 . Schizophrenia Research Forum: News . schizophreniaforum.org . 2008-08-21.
  11. Iqbal. Zafar. Vandeweyer. Geert. van der Voet. Monique. Waryah. Ali Muhammad. Zahoor. Muhammad Yasir. Besseling. Judith A.. Roca. Laura Tomas. Vulto-van Silfhout. Anneke T.. Nijhof. Bonnie. Kramer. Jamie M.. Van der Aa. Nathalie. Ansar. Muhammad. Peeters. Hilde. Helsmoortel. Celine. Gilissen. Christian. Vissers. Lisenka. Veltman. Joris A.. de Brouwer. Arjan P. M.. Kooy. R. Frank. Riazuddin. Sheikh. Schenck. Annette. van Bokhoven. Hans. Rooms. Liesbeth. Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders. Human Molecular Genetics. 2013. 0964-6906. 10.1093/hmg/ddt043. 22. 10. 1960–1970. 23390136. free.