Literature DB >> 17490620

Induction of high STAT1 expression in transgenic mice with LQTS and heart failure.

Ling Wu1, Stephen R Archacki, Teng Zhang, Qing K Wang.   

Abstract

Cardiac-specific expression of the N1325S mutation of SCN5A in transgenic mouse hearts (TG-NS) resulted in long QT syndrome (LQTS), ventricular arrhythmias (VT), and heart failure. In this study we carried out oligonucleotide mircoarray analysis to identify genes that are differentially expressed in the TG-NS mouse hearts. We identified 33 genes in five different functional groups that showed differential expression. None of the 33 genes are ion channel genes. STAT1, which encodes a transcription factor involved in apoptosis and interferon response, showed the most significant difference of expression between TG-NS and control mice (a nearly 10-fold increase in expression, P=4x10(-6)). The results were further confirmed by quantitative real-time PCR and Western blot analyses. Accordingly, many interferon response genes also showed differential expression in TG-NS hearts. This study represents the first microarray analysis for LQTS and implicates STAT1 in the pathogenesis and progression of LQTS and heart failure.

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Year:  2007        PMID: 17490620      PMCID: PMC3505674          DOI: 10.1016/j.bbrc.2007.04.119

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  24 in total

1.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

Authors:  K J Livak; T D Schmittgen
Journal:  Methods       Date:  2001-12       Impact factor: 3.608

2.  The gene expression fingerprint of human heart failure.

Authors:  Fen-Lai Tan; Christine S Moravec; Jianbo Li; Carolyn Apperson-Hansen; Patrick M McCarthy; James B Young; Meredith Bond
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-12       Impact factor: 11.205

3.  Post-transcriptional alterations in the expression of cardiac Na+ channel subunits in chronic heart failure.

Authors:  Stephen Zicha; Victor A Maltsev; Stanley Nattel; Hani N Sabbah; Albertas I Undrovinas
Journal:  J Mol Cell Cardiol       Date:  2004-07       Impact factor: 5.000

4.  Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel.

Authors:  M E Gellens; A L George; L Q Chen; M Chahine; R Horn; R L Barchi; R G Kallen
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-15       Impact factor: 11.205

5.  Ischemia-induced STAT-1 expression and activation play a critical role in cardiomyocyte apoptosis.

Authors:  A Stephanou; B K Brar; T M Scarabelli; A K Jonassen; D M Yellon; M S Marber; R A Knight; D S Latchman
Journal:  J Biol Chem       Date:  2000-04-07       Impact factor: 5.157

6.  Mechanisms by which SCN5A mutation N1325S causes cardiac arrhythmias and sudden death in vivo.

Authors:  Xiao-Li Tian; Sandro L Yong; Xiaoping Wan; Ling Wu; Mina K Chung; Patrick J Tchou; David S Rosenbaum; David R Van Wagoner; Glenn E Kirsch; Qing Wang
Journal:  Cardiovasc Res       Date:  2004-02-01       Impact factor: 10.787

7.  Localization of Nav1.5 sodium channel protein in the mouse brain.

Authors:  Ling Wu; Kazutoshi Nishiyama; Joe G Hollyfield; Qing Wang
Journal:  Neuroreport       Date:  2002-12-20       Impact factor: 1.837

Review 8.  STAT-1: a novel regulator of apoptosis.

Authors:  Anastasis Stephanou; David S Latchman
Journal:  Int J Exp Pathol       Date:  2003-12       Impact factor: 1.925

9.  Identification of new genes differentially expressed in coronary artery disease by expression profiling.

Authors:  Stephen R Archacki; George Angheloiu; Xiao-Li Tian; Fen Lai Tan; Nick DiPaola; Gong-Qing Shen; Christine Moravec; Stephen Ellis; Eric J Topol; Qing Wang
Journal:  Physiol Genomics       Date:  2003-09-29       Impact factor: 3.107

Review 10.  Transcription protein STAT1: biology and relation to cancer.

Authors:  L Adámková; K Soucková; J Kovarík
Journal:  Folia Biol (Praha)       Date:  2007       Impact factor: 0.906

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  4 in total

1.  LQTS mutation N1325S in cardiac sodium channel gene SCN5A causes cardiomyocyte apoptosis, cardiac fibrosis and contractile dysfunction in mice.

Authors:  Teng Zhang; Sandro L Yong; Jeanne K Drinko; Zoran B Popović; John C Shryock; Luiz Belardinelli; Qing Kenneth Wang
Journal:  Int J Cardiol       Date:  2009-09-17       Impact factor: 4.164

2.  Nemo-Like Kinase (NLK) Is a Pathological Signaling Effector in the Mouse Heart.

Authors:  Ruijie Liu; Hadi Khalil; Suh-Chin J Lin; Michelle A Sargent; Allen J York; Jeffery D Molkentin
Journal:  PLoS One       Date:  2016-10-20       Impact factor: 3.240

3.  Coherent functional modules improve transcription factor target identification, cooperativity prediction, and disease association.

Authors:  Konrad J Karczewski; Michael Snyder; Russ B Altman; Nicholas P Tatonetti
Journal:  PLoS Genet       Date:  2014-02-06       Impact factor: 5.917

4.  Identification of potentially relevant genes for myocardial infarction using RNA sequencing data analysis.

Authors:  Qiang Zhao; Ke Wu; Nannan Li; Zhengmei Li; Fenglin Jin
Journal:  Exp Ther Med       Date:  2017-11-28       Impact factor: 2.447

  4 in total

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