Hand factors as regulators of cardiac morphogenesis and implications for congenital heart defects
- PMID: 21462297
- PMCID: PMC3119928
- DOI: 10.1002/bdra.20796
Hand factors as regulators of cardiac morphogenesis and implications for congenital heart defects
Abstract
Almost 15 years of careful study have established the related basic Helix-Loop-Helix (bHLH) transcription factors Hand1 and Hand2 as critical for heart development across evolution. Hand factors make broad contributions, revealed through animal models, to the development of multiple cellular lineages that ultimately contribute to the heart. They perform critical roles in ventricular cardiomyocyte growth, differentiation, morphogenesis, and conduction. They are also important for the proper development of the cardiac outflow tract, epicardium, and endocardium. Molecularly, they function both through DNA binding and through protein-protein interactions, which are regulated transcriptionally, posttranscriptionally by microRNAs, and posttranslationally through phosphoregulation. Although direct Hand factor transcriptional targets are progressively being identified, confirmed direct targets of Hand factor transcriptional activity in the heart are limited. Identification of these targets will be critical to model the mechanisms by which Hand factor bHLH interactions affect developmental pathways. Improved understanding of Hand factor-mediated transcriptional cascades will be necessary to determine how Hand factor dysregulation translates to human disease phenotypes. This review summarizes the insight that animal models have provided into the regulation and function of these factors during heart development, in addition to the recent findings that suggest roles for HAND1 and HAND2 in human congenital heart disease.
Copyright © 2011 Wiley-Liss, Inc.
Similar articles
-
HAND transcription factors cooperatively specify the aorta and pulmonary trunk.Dev Biol. 2021 Aug;476:1-10. doi: 10.1016/j.ydbio.2021.03.011. Epub 2021 Mar 20. Dev Biol. 2021. PMID: 33757801 Free PMC article.
-
Gene replacement strategies to test the functional redundancy of basic helix-loop-helix transcription factor.Pediatr Cardiol. 2010 Apr;31(3):438-48. doi: 10.1007/s00246-010-9669-x. Epub 2010 Feb 14. Pediatr Cardiol. 2010. PMID: 20155416 Free PMC article. Review.
-
HAND1 loss-of-function within the embryonic myocardium reveals survivable congenital cardiac defects and adult heart failure.Cardiovasc Res. 2020 Mar 1;116(3):605-618. doi: 10.1093/cvr/cvz182. Cardiovasc Res. 2020. PMID: 31286141 Free PMC article.
-
Hand Factors in Cardiac Development.Anat Rec (Hoboken). 2019 Jan;302(1):101-107. doi: 10.1002/ar.23910. Epub 2018 Oct 5. Anat Rec (Hoboken). 2019. PMID: 30288953 Free PMC article. Review.
-
A bHLH code for cardiac morphogenesis.Pediatr Cardiol. 2010 Apr;31(3):318-24. doi: 10.1007/s00246-009-9608-x. Epub 2009 Dec 24. Pediatr Cardiol. 2010. PMID: 20033146 Free PMC article. Review.
Cited by
-
Unique gene program of rat small resistance mesenteric arteries as revealed by deep RNA sequencing.Physiol Rep. 2015 Jul;3(7):e12450. doi: 10.14814/phy2.12450. Physiol Rep. 2015. PMID: 26156969 Free PMC article.
-
An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality.Genes Dev. 2018 Mar 1;32(5-6):373-388. doi: 10.1101/gad.307330.117. Epub 2018 Mar 19. Genes Dev. 2018. PMID: 29555651 Free PMC article.
-
Different Cardiac Anomalies in Mother and Son with 4q-Syndrome.Case Rep Genet. 2015;2015:932651. doi: 10.1155/2015/932651. Epub 2015 Aug 31. Case Rep Genet. 2015. PMID: 26417463 Free PMC article.
-
The HAND1 frameshift A126FS mutation does not cause hypoplastic left heart syndrome in mice.Cardiovasc Res. 2017 Dec 1;113(14):1732-1742. doi: 10.1093/cvr/cvx166. Cardiovasc Res. 2017. PMID: 29016838 Free PMC article.
-
Rare copy number variants in patients with congenital conotruncal heart defects.Birth Defects Res. 2017 Mar 1;109(4):271-295. doi: 10.1002/bdra.23609. Epub 2017 Feb 13. Birth Defects Res. 2017. PMID: 28398664 Free PMC article.
References
-
- Ambros V. The functions of animal microRNAs. Nature. 2004;431(7006):350–355. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical