Literature DB >> 20006674

Differential expression of exon 5 splice variants of sodium channel alpha subunit mRNAs in the developing mouse brain.

E V Gazina1, K L Richards, M B C Mokhtar, E A Thomas, C A Reid, S Petrou.   

Abstract

Sodium channel alpha subunit genes expressed in the human brain, SCN1A, SCN2A, SCN3A and SCN8A, are subject to alternative splicing of coding exons 5N and 5A. In this study we examined expression of alpha subunit mRNA and exon 5 splicing in the developing mouse brain. Expression levels of Scn1a, Scn2a and Scn8a mRNAs increase postnatally, whereas Scn3a mRNA expression levels decrease. Scn1a mRNA contains only exon 5A, due to the absence of exon 5N in the mouse Scn1a gene. At birth, Scn2a is the only sodium channel alpha subunit mRNA that contains higher or equal amounts of the 5N isoform compared to the 5A isoform in most brain regions. In contrast, the predominant isoform of Scn3a and Scn8a mRNAs in the newborn mouse brain is 5A. 5N/5A ratios for each of the three mRNAs vary across brain regions, with cortex >or= hippocampus>thalamus>cerebellum. In all brain regions and for all three alpha subunits, 5N/5A ratios gradually decrease with age, levelling at a value between 0.1 and 0.2. These findings suggest potential involvement of common factors in the alternative splicing of exon 5 for all three transcripts, and that expression of these factors varies between brain regions and changes during development. Differences in the strength of exon 5N and/or exon 5A splice sites in Scn2a pre-mRNA as compared to Scn1a and Scn8a may underlie the observed differences in 5N/5A ratios in the three alpha subunit mRNAs. Crown Copyright 2010. Published by Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 20006674     DOI: 10.1016/j.neuroscience.2009.12.011

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  24 in total

1.  De novo and inherited SCN8A epilepsy mutations detected by gene panel analysis.

Authors:  Kameryn M Butler; Cristina da Silva; Yuval Shafir; James D Weisfeld-Adams; John J Alexander; Madhuri Hegde; Andrew Escayg
Journal:  Epilepsy Res       Date:  2016-11-06       Impact factor: 3.045

2.  Novel SCN3A variants associated with focal epilepsy in children.

Authors:  Carlos G Vanoye; Christina A Gurnett; Katherine D Holland; Alfred L George; Jennifer A Kearney
Journal:  Neurobiol Dis       Date:  2013-10-21       Impact factor: 5.996

3.  Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies.

Authors:  Gemma L Carvill; Krysta L Engel; Aishwarya Ramamurthy; J Nicholas Cochran; Jolien Roovers; Hannah Stamberger; Nicholas Lim; Amy L Schneider; Georgie Hollingsworth; Dylan H Holder; Brigid M Regan; James Lawlor; Lieven Lagae; Berten Ceulemans; E Martina Bebin; John Nguyen; Gregory S Barsh; Sarah Weckhuysen; Miriam Meisler; Samuel F Berkovic; Peter De Jonghe; Ingrid E Scheffer; Richard M Myers; Gregory M Cooper; Heather C Mefford
Journal:  Am J Hum Genet       Date:  2018-12-06       Impact factor: 11.025

Review 4.  Autism spectrum disorder: neuropathology and animal models.

Authors:  Merina Varghese; Neha Keshav; Sarah Jacot-Descombes; Tahia Warda; Bridget Wicinski; Dara L Dickstein; Hala Harony-Nicolas; Silvia De Rubeis; Elodie Drapeau; Joseph D Buxbaum; Patrick R Hof
Journal:  Acta Neuropathol       Date:  2017-06-05       Impact factor: 17.088

Review 5.  NaV1.1 channels and epilepsy.

Authors:  William A Catterall; Franck Kalume; John C Oakley
Journal:  J Physiol       Date:  2010-03-01       Impact factor: 5.182

Review 6.  A matter of space and time: Emerging roles of disease-associated proteins in neural development.

Authors:  Georgia Panagiotakos; Sergiu P Pasca
Journal:  Neuron       Date:  2021-11-29       Impact factor: 17.173

7.  Spliced isoforms of the cardiac Nav1.5 channel modify channel activation by distinct structural mechanisms.

Authors:  Adamo S Mancino; William G Glass; Yuhao Yan; Philip C Biggin; Derek Bowie
Journal:  J Gen Physiol       Date:  2022-03-17       Impact factor: 4.086

Review 8.  Progress in Understanding and Treating SCN2A-Mediated Disorders.

Authors:  Stephan J Sanders; Arthur J Campbell; Jeffrey R Cottrell; Rikke S Moller; Florence F Wagner; Angie L Auldridge; Raphael A Bernier; William A Catterall; Wendy K Chung; James R Empfield; Alfred L George; Joerg F Hipp; Omar Khwaja; Evangelos Kiskinis; Dennis Lal; Dheeraj Malhotra; John J Millichap; Thomas S Otis; Steven Petrou; Geoffrey Pitt; Leah F Schust; Cora M Taylor; Jennifer Tjernagel; John E Spiro; Kevin J Bender
Journal:  Trends Neurosci       Date:  2018-04-23       Impact factor: 13.837

9.  Alternative splicing modulates inactivation of type 1 voltage-gated sodium channels by toggling an amino acid in the first S3-S4 linker.

Authors:  Emily V Fletcher; Dimitri M Kullmann; Stephanie Schorge
Journal:  J Biol Chem       Date:  2011-09-02       Impact factor: 5.157

10.  Splice variants of Na(V)1.7 sodium channels have distinct β subunit-dependent biophysical properties.

Authors:  Clare Farmer; James J Cox; E V Fletcher; C Geoffrey Woods; John N Wood; Stephanie Schorge
Journal:  PLoS One       Date:  2012-07-24       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.