Details

Autor(en) / Beteiligte

• Lin, Honghuang, PhD
• Dolmatova, Elena V., MD
• Morley, Michael P., PhD
• Lunetta, Kathryn L., PhD
• McManus, David D., MD, ScM
• Magnani, Jared W., MD, MSc
• Margulies, Kenneth B., MD
• Hakonarson, Hakon, MD, PhD
• del Monte, Federica, MD, PhD
• Benjamin, Emelia J., MD, ScM
• Cappola, Thomas P., MD, ScM
• Ellinor, Patrick T., MD, PhD

Titel

Gene expression and genetic variation in human atria

Ist Teil von

• Heart rhythm, 2014-02, Vol.11 (2), p.266-271

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2014

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Background The human left and right atria have different susceptibilities to develop atrial fibrillation (AF). However, the molecular events related to structural and functional changes that enhance AF susceptibility are still poorly understood. Objective The purpose of this study was to characterize gene expression and genetic variation in human atria. Methods We studied the gene expression profiles and genetic variations in 53 left atrial and 52 right atrial tissue samples collected from the Myocardial Applied Genomics Network (MAGNet) repository. The tissues were collected from heart failure patients undergoing transplantation and from unused organ donor hearts with normal ventricular function. Gene expression was profiled using the Affymetrix GeneChip Human Genome U133A Array. Genetic variation was profiled using the Affymetrix Genome-Wide Human SNP Array 6.0. Results We found that 109 genes were differentially expressed between left and right atrial tissues. A total of 187 and 259 significant cis -associations between transcript levels and genetic variants were identified in left and right atrial tissues, respectively. We also found that a single nucleotide polymorphism at a known AF locus, rs3740293, was associated with the expression of MYOZ1 in both left and right atrial tissues. Conclusion We found a distinct transcriptional profile between the right and left atrium and extensive cis -associations between atrial transcripts and common genetic variants. Our results implicate MYOZ1 as the causative gene at the chromosome 10q22 locus for AF.