Literature DB >> 15286995

Floxed allele for conditional inactivation of the voltage-gated sodium channel Scn8a (NaV1.6).

Stephen I Levin1, Miriam H Meisler.   

Abstract

The sodium channel gene Scn8a encodes the channel NaV1.6, which is widely distributed in the central and peripheral nervous system. NaV1.6 is the major channel at the nodes of Ranvier in myelinated axons. Mutant alleles of mouse Scn8a result in neurological disorders including ataxia, tremor, paralysis, and dystonia. We generated a floxed allele of Scn8a by inserting loxP sites around the first coding exon. The initial targeted allele containing the neo-cassette was a severe hypomorph. In vivo deletion of the neo-cassette by Flp recombinase produced a floxed allele that generates normal expression of NaV1.6 protein. Ubiquitous deletion of the floxed exon by Cre recombinase in ZP3-Cre transgenic mice produced the Scn8a(del) allele. The null phenotype of Scn8a(del) homozygotes confirms the in vivo inactivation of Scn8a. Conditional inactivation of the floxed allele will make it possible to circumvent the lethality that results from complete loss of Scn8a in order to investigate the physiologic role of NaV1.6 in subpopulations of neurons. 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15286995     DOI: 10.1002/gene.20050

Source DB:  PubMed          Journal:  Genesis        ISSN: 1526-954X            Impact factor:   2.487


  18 in total

Review 1.  Sodium channel mutations in epilepsy and other neurological disorders.

Authors:  Miriam H Meisler; Jennifer A Kearney
Journal:  J Clin Invest       Date:  2005-08       Impact factor: 14.808

2.  Persistent Nav1.6 current at axon initial segments tunes spike timing of cerebellar granule cells.

Authors:  Nancy Osorio; Laurence Cathala; Miriam H Meisler; Marcel Crest; Jacopo Magistretti; Patrick Delmas
Journal:  J Physiol       Date:  2010-02-15       Impact factor: 5.182

3.  Interaction of voltage-gated sodium channel Nav1.6 (SCN8A) with microtubule-associated protein Map1b.

Authors:  Janelle E O'Brien; Lisa M Sharkey; Christina N Vallianatos; Chongyang Han; Julie C Blossom; Ting Yu; Stephen G Waxman; Sulayman D Dib-Hajj; Miriam H Meisler
Journal:  J Biol Chem       Date:  2012-04-03       Impact factor: 5.157

4.  Modeling human epilepsy by TALEN targeting of mouse sodium channel Scn8a.

Authors:  Julie M Jones; Miriam H Meisler
Journal:  Genesis       Date:  2013-12-12       Impact factor: 2.487

5.  The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking.

Authors:  Lisa M Sharkey; Xiaoyang Cheng; Valerie Drews; David A Buchner; Julie M Jones; Monica J Justice; Stephen G Waxman; Sulayman D Dib-Hajj; Miriam H Meisler
Journal:  J Neurosci       Date:  2009-03-04       Impact factor: 6.167

6.  Mice hypomorphic for Atr have increased DNA damage and abnormal checkpoint response.

Authors:  Ryan L Ragland; Martin F Arlt; Elizabeth D Hughes; Thomas L Saunders; Thomas W Glover
Journal:  Mamm Genome       Date:  2009-06-07       Impact factor: 2.957

7.  Rescue of neurodegeneration in the Fig4 null mouse by a catalytically inactive FIG4 transgene.

Authors:  Guy M Lenk; Christen M Frei; Ashley C Miller; Rachel C Wallen; Yevgeniya A Mironova; Roman J Giger; Miriam H Meisler
Journal:  Hum Mol Genet       Date:  2015-11-24       Impact factor: 6.150

8.  Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance.

Authors:  Christopher D Makinson; Brian S Tanaka; Tyra Lamar; Alan L Goldin; Andrew Escayg
Journal:  Neurobiol Dis       Date:  2014-04-02       Impact factor: 5.996

9.  Role of sodium channel subtype in action potential generation by neocortical pyramidal neurons.

Authors:  Efrat Katz; Ohad Stoler; Anja Scheller; Yana Khrapunsky; Sandra Goebbels; Frank Kirchhoff; Michael J Gutnick; Fred Wolf; Ilya A Fleidervish
Journal:  Proc Natl Acad Sci U S A       Date:  2018-07-10       Impact factor: 11.205

10.  Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.

Authors:  Ligia A Papale; Barbara Beyer; Julie M Jones; Lisa M Sharkey; Sergio Tufik; Michael Epstein; Verity A Letts; Miriam H Meisler; Wayne N Frankel; Andrew Escayg
Journal:  Hum Mol Genet       Date:  2009-03-02       Impact factor: 6.150

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