Gene Expression Profiling of the Forming Atrioventricular Node Using a Novel Tbx3-Based Node-Specific Transgenic Reporter

• Published in: Circulation research 2009-07, Vol.105 (1), p.61-69
• Main Authors: Horsthuis, Thomas, Buermans, Henk P.J, Brons, Janynke F, Verkerk, Arie O, Bakker, Martijn L, Wakker, Vincent, Clout, Danielle E.W, Moorman, Antoon F.M, ʼt Hoen, Peter A.C, Christoffels, Vincent M
• Format: Article
• Language: English
• Subjects: Animals; Atrioventricular Node; Biological and medical sciences; Calcium Channels - genetics; Chromosomes, Artificial, Bacterial; Embryo, Mammalian; Fundamental and applied biological sciences. Psychology; Gene Expression Profiling - methods; Genes, Reporter; Green Fluorescent Proteins; Mice; Mice, Transgenic; Nerve Tissue Proteins - genetics; Potassium Channels - genetics; Sodium Channels - genetics; T-Box Domain Proteins - genetics; Vertebrates: cardiovascular system
• ISSN: 0009-7330; 1524-4571
• DOI: 10.1161/CIRCRESAHA.108.192443

The atrioventricular (AV) node is a recurrent source of potentially life-threatening arrhythmias. Nevertheless, limited data are available on its developmental control or molecular phenotype. We used a novel AV nodal myocardium–specific reporter mouse to gain insight into the gene programs determining the formation and phenotype of the developing AV node. In this reporter, green fluorescent protein (GFP) expression was driven by a 160-kbp bacterial artificial chromosome with Tbx3 and flanking sequences. GFP was selectively active in the AV canal of embryos and AV node of adults, whereas the Tbx3-positive AV bundle and sinus node were devoid of GFP, demonstrating that distinct regulatory sequences and pathways control expression in the components of the conduction system. Fluorescent AV nodal and complementary Nppa-positive chamber myocardial cell populations of embryonic day 10.5 embryos and of embryonic day 17.5 fetuses were purified using fluorescence-activated cell sorting, and their expression profiles were assessed by genome-wide microarray analysis, providing valuable information concerning their molecular identities. We constructed a comprehensive list of sodium, calcium, and potassium channel genes specific for developing nodal or chamber myocardium. Furthermore, the data revealed that the AV node and the chamber (working) myocardium phenotypes diverge during development but that the functional gene classes characterizing both subtypes are maintained. One of the repertoires identified in the AV node–specific gene profiles consists of multiple neurotrophic factors and semaphorins, not yet appreciated to play a role in nodal development, revealing shared characteristics between nodal and nervous system development.