4.7 Article

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

Journal

DEVELOPMENT
Volume 136, Issue 15, Pages 2665-2674

Publisher

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.038562

Keywords

Cardiac conduction system; Arrhythmia; Atrioventricular Node; Cx30.2; Gata4; Mouse

Funding

  1. NHLBI NIH HHS [1K08HL094699-01, K08 HL094699] Funding Source: Medline

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available