TY - JOUR
T1 - Genetic Dissection of a Super Enhancer Controlling the Nppa-Nppb Cluster in the Heart
AU - Man, Joyce Ck
AU - van Duijvenboden, Karel
AU - Krijger, Peter Hl
AU - Hooijkaas, Ingeborg B
AU - van der Made, Ingeborg
AU - de Gier-de Vries, Corrie
AU - Wakker, Vincent
AU - Creemers, Esther E
AU - de Laat, Wouter
AU - Boukens, Bastiaan J
AU - Christoffels, Vincent M
PY - 2020/10/27
Y1 - 2020/10/27
N2 - Rationale: Atrial and B-type natriuretic peptide, encoded by the clustered genes Nppa and Nppb, are important prognostic, diagnostic and therapeutic proteins in cardiac disease. The spatio-temporal expression pattern and stress-induction of the Nppa and Nppb are tightly regulated, possibly involving their co-regulation by an evolutionary conserved enhancer cluster.Objective: To explore the physiological functions of the enhancer cluster and elucidate the genomic mechanism underlying Nppa-Nppb co-regulation in vivo. Methods and Results: By analyzing epigenetic data we uncovered an enhancer cluster with super enhancer characteristics upstream of Nppb. Using CRISPR/Cas9 genome editing, the enhancer cluster or parts thereof, Nppb and flanking regions or the entire genomic block spanning Nppa-Nppb, respectively, were deleted from the mouse genome. The impact on gene regulation and phenotype of the respective mouse lines was investigated by transcriptomic, epigenomic and phenotypic analyses. The enhancer cluster was essential for prenatal and postnatal ventricular expression of Nppa and Nppb, but not of any other gene. Enhancer cluster-deficient mice showed enlarged hearts before and after birth, similar to Nppa-Nppb compound knockout mice we generated. Analysis of the other deletion alleles indicated the enhancer cluster engages the promoters of Nppa and Nppb in a competitive rather than a cooperative mode, resulting in increased Nppa expression when Nppb and flanking sequences were deleted. The enhancer cluster maintained its active epigenetic state and selectivity in when its target genes are absent. In enhancer cluster-deficient animals, Nppa was induced but remained low in the post-myocardial infarction border zone and in the hypertrophic ventricle, involving regulatory sequences proximal to Nppa. Conclusions: Coordinated ventricular expression of Nppa and Nppb is controlled in a competitive manner by a shared super enhancer, which is also required to augment stress-induced expression and to prevent premature hypertrophy.
AB - Rationale: Atrial and B-type natriuretic peptide, encoded by the clustered genes Nppa and Nppb, are important prognostic, diagnostic and therapeutic proteins in cardiac disease. The spatio-temporal expression pattern and stress-induction of the Nppa and Nppb are tightly regulated, possibly involving their co-regulation by an evolutionary conserved enhancer cluster.Objective: To explore the physiological functions of the enhancer cluster and elucidate the genomic mechanism underlying Nppa-Nppb co-regulation in vivo. Methods and Results: By analyzing epigenetic data we uncovered an enhancer cluster with super enhancer characteristics upstream of Nppb. Using CRISPR/Cas9 genome editing, the enhancer cluster or parts thereof, Nppb and flanking regions or the entire genomic block spanning Nppa-Nppb, respectively, were deleted from the mouse genome. The impact on gene regulation and phenotype of the respective mouse lines was investigated by transcriptomic, epigenomic and phenotypic analyses. The enhancer cluster was essential for prenatal and postnatal ventricular expression of Nppa and Nppb, but not of any other gene. Enhancer cluster-deficient mice showed enlarged hearts before and after birth, similar to Nppa-Nppb compound knockout mice we generated. Analysis of the other deletion alleles indicated the enhancer cluster engages the promoters of Nppa and Nppb in a competitive rather than a cooperative mode, resulting in increased Nppa expression when Nppb and flanking sequences were deleted. The enhancer cluster maintained its active epigenetic state and selectivity in when its target genes are absent. In enhancer cluster-deficient animals, Nppa was induced but remained low in the post-myocardial infarction border zone and in the hypertrophic ventricle, involving regulatory sequences proximal to Nppa. Conclusions: Coordinated ventricular expression of Nppa and Nppb is controlled in a competitive manner by a shared super enhancer, which is also required to augment stress-induced expression and to prevent premature hypertrophy.
U2 - 10.1161/CIRCRESAHA.120.317045
DO - 10.1161/CIRCRESAHA.120.317045
M3 - Article
C2 - 33107387
SN - 0009-7330
JO - Circulation Research
JF - Circulation Research
ER -