Cx30.2 enhancer analysis identifies Gata4 as a novel regulator of atrioventricular delay

被引:56
作者
Munshi, Nikhil V. [1 ,2 ]
McAnally, John [1 ]
Bezprozvannaya, Svetlana [1 ]
Berry, Jeff M. [1 ,2 ]
Richardson, James A. [3 ]
Hill, Joseph A. [1 ,2 ]
Olson, Eric N. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
来源
DEVELOPMENT | 2009年 / 136卷 / 15期
关键词
Cardiac conduction system; Arrhythmia; Atrioventricular Node; Cx30.2; Gata4; Mouse; CARDIAC CONDUCTION SYSTEM; TRANSCRIPTION FACTOR TBX5; CONGENITAL HEART-DISEASE; FUNCTIONAL-PROPERTIES; IMPULSE PROPAGATION; GENE-EXPRESSION; MOUSE; NKX2-5; CONNEXIN30.2; NODE;
D O I
10.1242/dev.038562
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The cardiac conduction system comprises a specialized tract of electrically coupled cardiomyocytes responsible for impulse propagation through the heart. Abnormalities in cardiac conduction are responsible for numerous forms of cardiac arrhythmias, but relatively little is known about the gene regulatory mechanisms that control the formation of the conduction system. We demonstrate that a distal enhancer for the connexin 30.2 (Cx30.2, also known as Gjd3) gene, which encodes a gap junction protein required for normal atrioventricular (AV) delay in mice, is necessary and sufficient to direct expression to the developing AV conduction system (AVCS). Moreover, we show that this enhancer requires Tbx5 and Gata4 for proper expression in the conduction system, and Gata4(+/-) mice have short PR intervals indicative of accelerated AV conduction. Thus, our results implicate Gata4 in conduction system function and provide a clearer understanding of the transcriptional pathways that impact normal AV delay.
引用
收藏
页码:2665 / 2674
页数:10
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