Literature DB >> 21394759

Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms.

Fatima Banine1, Valerie Matagne, Larry S Sherman, Sergio R Ojeda.   

Abstract

Fxyd1 encodes a trans-membrane protein that modulates Na(+) ,K(+) -ATPase activity and is a substrate for multiple protein kinases. Fxyd1 expression is repressed by methyl CpG-binding protein 2 (Mecp2) in the frontal cortex (FC) but not in the cerebellum (CB) of the mouse brain. Consistently with these observations, FXYD1 mRNA abundance is increased in the FC of Rett syndrome (RTT) patients with MECP2 mutations. Because Fxyd1 is implicated in the regulation of neuronal excitability, understanding how Fxyd1 expression is controlled is important. Here we report that basal expression of Fxyd1a and Fxyd1b, the two main alternatively spliced forms of Fxyd1 mRNA, is lower in the FC than in the CB. This difference is accompanied by increased Mecp2 recruitment to the promoter region of these two Fxyd1 mRNA forms. DNA methylation of both promoters is more frequent in the FC than in the CB, and in both cases the most frequently methylated CpG dinucleotides are adjacent to [A/T](4) sequences required for high-affinity Mecp2 binding. Consistently with these features of epigenetic silencing, histone 3 acetylated at lysines 9 and 14 (H3K9/14ac) and histone 3 methylated at lysine 4 (H3K4me3), both activating histone marks, were associated with the Fxyd1 promoter to a lesser degree in the FC than in the CB. These results indicate that differential Fxyd1 expression in these two brain regions is, at least in part, regulated by an epigenetic mechanism involving increased DNA methylation of the two alternative Fxyd1 promoters, enhanced Mecp2 recruitment, and reduced association of activating histones.
Copyright © 2011 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21394759      PMCID: PMC3261072          DOI: 10.1002/jnr.22608

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  69 in total

Review 1.  Increase of functional diversity by alternative splicing.

Authors:  Evgenia V Kriventseva; Ina Koch; Rolf Apweiler; Martin Vingron; Peer Bork; Mikhail S Gelfand; Shamil Sunyaev
Journal:  Trends Genet       Date:  2003-03       Impact factor: 11.639

Review 2.  Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals.

Authors:  Rudolf Jaenisch; Adrian Bird
Journal:  Nat Genet       Date:  2003-03       Impact factor: 38.330

3.  Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation.

Authors:  Mona D Shahbazian; Barbara Antalffy; Dawna L Armstrong; Huda Y Zoghbi
Journal:  Hum Mol Genet       Date:  2002-01-15       Impact factor: 6.150

4.  Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.

Authors:  R Z Chen; S Akbarian; M Tudor; R Jaenisch
Journal:  Nat Genet       Date:  2001-03       Impact factor: 38.330

5.  A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.

Authors:  J Guy; B Hendrich; M Holmes; J E Martin; A Bird
Journal:  Nat Genet       Date:  2001-03       Impact factor: 38.330

6.  Gene structure and expression of phospholemman in mouse.

Authors:  R C Bogaev; L G Jia; Y M Kobayashi; C J Palmer; J P Mounsey; J R Moorman; L R Jones; A L Tucker
Journal:  Gene       Date:  2001-06-13       Impact factor: 3.688

7.  Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain.

Authors:  Matthew Tudor; Schahram Akbarian; Richard Z Chen; Rudolf Jaenisch
Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-13       Impact factor: 11.205

8.  Phospholemman (FXYD1) associates with Na,K-ATPase and regulates its transport properties.

Authors:  Gilles Crambert; Maria Fuzesi; Haim Garty; Steven Karlish; Kathi Geering
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-08       Impact factor: 11.205

9.  Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.

Authors:  Mona Shahbazian; Juan Young; Lisa Yuva-Paylor; Corinne Spencer; Barbara Antalffy; Jeffrey Noebels; Dawna Armstrong; Richard Paylor; Huda Zoghbi
Journal:  Neuron       Date:  2002-07-18       Impact factor: 17.173

10.  Phospholemman, a single-span membrane protein, is an accessory protein of Na,K-ATPase in cerebellum and choroid plexus.

Authors:  Marina S Feschenko; Claudia Donnet; Randall K Wetzel; Natalya K Asinovski; Larry R Jones; Kathleen J Sweadner
Journal:  J Neurosci       Date:  2003-03-15       Impact factor: 6.167

View more
  8 in total

1.  Epileptogenesis: can the science of epigenetics give us answers?

Authors:  Farah D Lubin
Journal:  Epilepsy Curr       Date:  2012-05       Impact factor: 7.500

2.  Correcting deregulated Fxyd1 expression rescues deficits in neuronal arborization and potassium homeostasis in MeCP2 deficient male mice.

Authors:  Valerie Matagne; Joyce Wondolowski; Matthew Frerking; Mohammad Shahidullah; Nicholas A Delamere; Ursula S Sandau; Sarojini Budden; Sergio R Ojeda
Journal:  Brain Res       Date:  2018-06-12       Impact factor: 3.252

3.  Correcting deregulated Fxyd1 expression ameliorates a behavioral impairment in a mouse model of Rett syndrome.

Authors:  Valerie Matagne; Sarojini Budden; Sergio R Ojeda; Jacob Raber
Journal:  Brain Res       Date:  2012-12-14       Impact factor: 3.252

4.  Brg1 directly regulates Olig2 transcription and is required for oligodendrocyte progenitor cell specification.

Authors:  Steven Matsumoto; Fatima Banine; Kerstin Feistel; Scott Foster; Rubing Xing; Jaime Struve; Larry S Sherman
Journal:  Dev Biol       Date:  2016-04-08       Impact factor: 3.582

5.  Epigenetic remodelling of Fxyd1 promoters in developing heart and brain tissues.

Authors:  Mariella Cuomo; Ermanno Florio; Rosa Della Monica; Davide Costabile; Michela Buonaiuto; Teodolinda Di Risi; Giulia De Riso; Antonella Sarnataro; Sergio Cocozza; Roberta Visconti; Lorenzo Chiariotti
Journal:  Sci Rep       Date:  2022-04-19       Impact factor: 4.996

Review 6.  Transcriptional regulators of Na,K-ATPase subunits.

Authors:  Zhiqin Li; Sigrid A Langhans
Journal:  Front Cell Dev Biol       Date:  2015-10-26

7.  Promoter-like sequences regulating transcriptional activity in neurexin and neuroligin genes.

Authors:  Fabian Runkel; Astrid Rohlmann; Carsten Reissner; Stefan-Martin Brand; Markus Missler
Journal:  J Neurochem       Date:  2013-08-21       Impact factor: 5.372

8.  Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia.

Authors:  Boris Chaumette; Vladimir Ferrafiat; Amirthagowri Ambalavanan; Alice Goldenberg; Alexandre Dionne-Laporte; Dan Spiegelman; Patrick A Dion; Priscille Gerardin; Claudine Laurent; David Cohen; Judith Rapoport; Guy A Rouleau
Journal:  Mol Psychiatry       Date:  2018-06-12       Impact factor: 15.992

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.