TY - JOUR
T1 - Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
AU - Jimenez, Jesus
AU - Rentschler, Stacey L.
N1 - Funding Information:
This study was supported by Grants T32 HL007081 (J. Jimenez), R01 HL130212 (S. Rentschler), and UG3HL141800 (S. Rentschler) from the National Institutes of Health. Rentschler holds a Career Award for Medical Scientists from the Burroughs Wellcome Fund.
Publisher Copyright:
© 2019, The Author(s).
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Spatiotemporal gene expression during cardiac development is a highly regulated process. Activation of key signaling pathways involved in electrophysiological programming, such as Notch and Wnt signaling, occurs in early cardiovascular development and these pathways are reactivated during pathologic remodeling. Direct targets of these signaling pathways have also been associated with inherited arrhythmias such as Brugada syndrome and arrhythmogenic cardiomyopathy. In addition, evidence is emerging from animal models that reactivation of Notch and Wnt signaling during cardiac pathology may predispose to acquired arrhythmias, underscoring the importance of elucidating the transcriptional and epigenetic effects on cardiac gene regulation. Here, we highlight specific examples where gene expression dictates electrophysiological properties in both normal and diseased hearts.
AB - Spatiotemporal gene expression during cardiac development is a highly regulated process. Activation of key signaling pathways involved in electrophysiological programming, such as Notch and Wnt signaling, occurs in early cardiovascular development and these pathways are reactivated during pathologic remodeling. Direct targets of these signaling pathways have also been associated with inherited arrhythmias such as Brugada syndrome and arrhythmogenic cardiomyopathy. In addition, evidence is emerging from animal models that reactivation of Notch and Wnt signaling during cardiac pathology may predispose to acquired arrhythmias, underscoring the importance of elucidating the transcriptional and epigenetic effects on cardiac gene regulation. Here, we highlight specific examples where gene expression dictates electrophysiological properties in both normal and diseased hearts.
KW - Electrophysiology
KW - Epigenetics
KW - HEY2
KW - Histone modification
KW - KCNIP2
UR - http://www.scopus.com/inward/record.url?scp=85069637935&partnerID=8YFLogxK
U2 - 10.1007/s00246-019-02160-w
DO - 10.1007/s00246-019-02160-w
M3 - Article
C2 - 31346662
AN - SCOPUS:85069637935
SN - 0172-0643
VL - 40
SP - 1325
EP - 1330
JO - Pediatric Cardiology
JF - Pediatric Cardiology
IS - 7
ER -