Whole Genome Expression Differences in Human Left and Right Atria Ascertained by RNA Sequencing

被引:56
作者
Hsu, Jeffrey [2 ,3 ]
Hanna, Peter
Van Wagoner, David R. [1 ,4 ]
Barnard, John
Serre, David [5 ]
Chung, Mina K. [4 ]
Smith, Jonathan D. [1 ,2 ,3 ]
机构
[1] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH 44195 USA
[2] Case Western Reserve Univ, Lerner Coll Med, Cleveland Clin, Dept Mol Med, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Cell Biol, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Dept Mol Cardiol, Cleveland, OH 44106 USA
[5] Case Western Reserve Univ, Cleveland Clin Lerner Res Inst, Genom Med Inst, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
arrhythmia; atrial fibrillation; atrium; gene expression; EMBRYONIC STEM-CELLS; GENE-EXPRESSION; FIBRILLATION; ALIGNMENT; SEQ; ACTIVATION; MICRORNAS; COMPLEXES; DISCOVERY; CHANNELS;
D O I
10.1161/CIRCGENETICS.111.961631
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-The left and right atria have different susceptibilities toward developing arrhythmias, with left atrial arrhythmias more commonly observed. To understand the molecular basis for such differences, we catalogued micro (mi) RNA and mRNA expression differences by next generation sequencing. Methods and Results-Four human left-right atrial pairs were subjected to whole-genome expression analyses via next-generation sequencing of small RNAs, including miRNAs, and poly-A-enriched mRNAs. Using a paired sample design, significant differences in the expression of 32 miRNAs were found in between the left and right atria at a probability value of <0.01. Hsa-miR-143 was the most highly expressed miRNA in the atria, as quantified by RNA sequencing. There were 746 and 2292 differentially expressed mRNAs between the left and right atria at false discovery rates of <0.001 and <0.05, respectively. Transcription factor binding elements within 2 kb of RefSeq genes were determined and specific motifs were identified that were enriched in differentially expressed genes. Similarly, specific miRNA target sequences in 3' UTRs were also enriched in differentially expressed genes. In addition, 11 novel noncoding RNAs of unknown function were found to be differentially expressed between the left and right atria. Conclusions-There are significant differences in miRNA and mRNA expression profiles between the left and right atria, which may yield insight into increased the arrhythmogenesis of the left atria. (Circ Cardiovasc Genet.2012;5:327-335.)
引用
收藏
页码:327 / 335
页数:9
相关论文
共 42 条
[1]   Activation of inward rectifier potassium channels accelerates atrial fibrillation in humans -: Evidence for a Reentrant mechanism [J].
Atienza, Felipe ;
Almendral, Jesus ;
Moreno, Javier ;
Vaidyanathan, Ravi ;
Talkachou, Arkazdi ;
Kalifa, Jerome ;
Arenal, Angel ;
Villacastin, Julian P. ;
Torrecilla, Esteban G. ;
Sanchez, Ana ;
Ploutz-Synder, Robert ;
Jalife, Jose ;
Berenfeld, Omer .
CIRCULATION, 2006, 114 (23) :2434-2442
[2]   Functional profiling of human atrial and ventricular gene expression [J].
Barth, AS ;
Merk, S ;
Arnoldi, E ;
Zwermann, L ;
Kloos, P ;
Gebauer, M ;
Steinmeyer, K ;
Bleich, M ;
Kääb, S ;
Pfeufer, A ;
Überfuhr, P ;
Dugas, M ;
Steinbeck, G ;
Nabauer, M .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2005, 450 (04) :201-208
[3]   Impact of atrial fibrillation on the risk of death [J].
Benjamin, EJ ;
Wolf, PA ;
D'Agostino, RB ;
Silbershatz, H ;
Kannel, WB ;
Levy, D .
CIRCULATION, 1998, 98 (10) :946-952
[4]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[5]   ChIP-Seq identification of weakly conserved heart enhancers [J].
Blow, Matthew J. ;
McCulley, David J. ;
Li, Zirong ;
Zhang, Tao ;
Akiyama, Jennifer A. ;
Holt, Amy ;
Plajzer-Frick, Ingrid ;
Shoukry, Malak ;
Wright, Crystal ;
Chen, Feng ;
Afzal, Veena ;
Bristow, James ;
Ren, Bing ;
Black, Brian L. ;
Rubin, Edward M. ;
Visel, Axel ;
Pennacchio, Len A. .
NATURE GENETICS, 2010, 42 (09) :806-U107
[6]   PITX2 Insufficiency Leads to Atrial Electrical and Structural Remodeling Linked to Arrhythmogenesis [J].
Chinchilla, Ana ;
Daimi, Houria ;
Lozano-Velasco, Estefania ;
Dominguez, Jorge N. ;
Caballero, Ricardo ;
Delpon, Eva ;
Tamargo, Juan ;
Cinca, Juan ;
Hove-Madsen, Leif ;
Aranega, Amelia E. ;
Franco, Diego .
CIRCULATION-CARDIOVASCULAR GENETICS, 2011, 4 (03) :269-U133
[7]   miR-145 and miR-143 regulate smooth muscle cell fate and plasticity [J].
Cordes, Kimberly R. ;
Sheehy, Neil T. ;
White, Mark P. ;
Berry, Emily C. ;
Morton, Sarah U. ;
Muth, Alecia N. ;
Lee, Ting-Hein ;
Miano, Joseph M. ;
Ivey, Kathryn N. ;
Srivastava, Deepak .
NATURE, 2009, 460 (7256) :705-U80
[8]   The miR-143-adducin3 pathway is essential for cardiac chamber morphogenesis [J].
Deacon, Dekker C. ;
Nevis, Kathleen R. ;
Cashman, Timothy J. ;
Zhou, Yong ;
Zhao, Long ;
Washko, Daniel ;
Guner-Ataman, Burcu ;
Burns, C. Geoffrey ;
Burns, Caroline E. .
DEVELOPMENT, 2010, 137 (11) :1887-1896
[9]   The pitx2 homeobox protein is required early for endoderm formation and nodal signaling [J].
Faucourt, M ;
Houliston, E ;
Besnardeau, L ;
Kimelman, D ;
Lepage, T .
DEVELOPMENTAL BIOLOGY, 2001, 229 (02) :287-306
[10]   Atrial myocardium derives from the posterior region of the second heart field, which acquires left-right identity as Pitx2c is expressed [J].
Galli, Daniela ;
Dominguez, Jorge N. ;
Zaffran, Stephane ;
Munk, Andrew ;
Brown, Nigel A. ;
Buckingham, Margaret E. .
DEVELOPMENT, 2008, 135 (06) :1157-1167