Over the last few decades, the study of congenital heart disease (CHD) has benefited from various model systems and the development of molecular biological techniques enabling the analysis of single gene as well as global effects. In this chapter, we first describe different models including CHD patients and their families, animal models ranging from invertebrates to mammals, and various cell culture systems. Moreover, techniques to experimentally manipulate these models are discussed. Second, we introduce cardiac phenotyping technologies comprising the analysis of mouse and cell culture models, live imaging of cardiogenesis, and histological methods for fixed hearts. Finally, the most important and latest molecular biotechniques are described. These include genotyping technologies, different applications of next-generation sequencing, and the analysis of transcriptome, epigenome, proteome, and metabolome. In summary, the models and technologies presented in this chapter are essential to study the function and development of the heart and to understand the molecular pathways underlying CHD.
Keywords: ATAC-seq; Animal models; Array comparative genomic hybridization; Array-CGH; CLIP; CRISPR; Caenorhabditis elegans; Cardiomyocytes; Cell culture; ChIP; ChIP-seq; Chicken; Chromatin immunoprecipitation; Clawed frog; DNA methylation; Drosophila melanogaster; ES cells; Embryonic stem cells; Epigenome; FACS; FISH; Fluorescence in situ hybridization; Fluorescence-activated cell sorting; Fruit fly; GWAS; Gallus gallus; Genome-wide association studies; Genotyping technologies; Histological analysis; Imaging; Immunohistochemistry; In situ hybridization; Induced pluripotent ES cells; MBD; MRI; MS; Magnetic resonance imaging; Mass spectrometry; Metabolome; Micro-CT; Micro-computed tomography; Morpholino oligonucleotides; Mouse; Mus musculus; NGS; NKX2-5; NMR; Nematode; Next-generation sequencing; Nuclear magnetic resonance spectroscopy; PAR-CLIP; Phenotyping; Proteome; RNA-seq; Rat; Rattus norvegicus; SILAC; SNPs; Sanger sequencing; Single-nucleotide polymorphisms; TALENs; Transcription activator-like effector nucleases; Transcriptome; Xenopus laevis; Yeast-two-hybrid; ZFN; Zebrafish; Zinc finger nucleases; iPSCs.
© 2024. The Author(s), under exclusive license to Springer Nature Switzerland AG.