A key area of focus in the field of epigenetics pertains the comprehension of the functional relevance of the epigenetic mechanisms occurring during embryogenesis to shape normal developmental trajectories and adult phenotypes. Strictly connected with this facet is the work investigating how environmental cues trigger reversible remodelling of embryonic epigenetic configurations and phenotype alterations that can be inherited over multiple generations.
Several lines of evidence highlighted that the small freshwater cyprinid Danio rerio, commonly known as zebrafish, is an excellent vertebrate model for research purposes in the field of epigenetics. The general strengths of zebrafish over concurrent models are well known: ease of husbandry and maintenance in laboratory, high fecundity, external fertilization, short life cycle and generation time. Beyond this, the increasing popularity of zebrafish for epigenetic research purposes is due to two main reasons. First, components of the epigenetic machinery have been widely characterized in zebrafish, showing overall conservation with mammals. No less important, zebrafish embryos are optically translucent and relatively permeable to a wide range of compounds, allowing non-invasive live imaging of morphogenesis and phenotypes following exposure to environmental stressors that challenge the epigenome. Altogether, these benefits also make zebrafish an outstanding model for large-scale screening of potential therapeutics targeting epigenetic regulatory mechanisms.
This Research Topic covers all aspects of zebrafish research aimed at improving our understanding of the role of epigenetic mechanisms in biological processes occurring especially, but not exclusively, during zebrafish embryogenesis. Authors are welcome to submit a wide range of article types falling under, but not limited to, the following topics:
- covalent modifications of DNA and histones;
- exchange of specialized histone variants into existing nucleosomes;
- nucleosome positioning and density;
- three-dimensional chromatin organization;
- noncoding RNAs and transcriptional regulatory networks.
A key area of focus in the field of epigenetics pertains the comprehension of the functional relevance of the epigenetic mechanisms occurring during embryogenesis to shape normal developmental trajectories and adult phenotypes. Strictly connected with this facet is the work investigating how environmental cues trigger reversible remodelling of embryonic epigenetic configurations and phenotype alterations that can be inherited over multiple generations.
Several lines of evidence highlighted that the small freshwater cyprinid Danio rerio, commonly known as zebrafish, is an excellent vertebrate model for research purposes in the field of epigenetics. The general strengths of zebrafish over concurrent models are well known: ease of husbandry and maintenance in laboratory, high fecundity, external fertilization, short life cycle and generation time. Beyond this, the increasing popularity of zebrafish for epigenetic research purposes is due to two main reasons. First, components of the epigenetic machinery have been widely characterized in zebrafish, showing overall conservation with mammals. No less important, zebrafish embryos are optically translucent and relatively permeable to a wide range of compounds, allowing non-invasive live imaging of morphogenesis and phenotypes following exposure to environmental stressors that challenge the epigenome. Altogether, these benefits also make zebrafish an outstanding model for large-scale screening of potential therapeutics targeting epigenetic regulatory mechanisms.
This Research Topic covers all aspects of zebrafish research aimed at improving our understanding of the role of epigenetic mechanisms in biological processes occurring especially, but not exclusively, during zebrafish embryogenesis. Authors are welcome to submit a wide range of article types falling under, but not limited to, the following topics:
- covalent modifications of DNA and histones;
- exchange of specialized histone variants into existing nucleosomes;
- nucleosome positioning and density;
- three-dimensional chromatin organization;
- noncoding RNAs and transcriptional regulatory networks.
