PUBLICATION
Generation and Characterization of a CRISPR/Cas9 -Induced 3-mst Deficient Zebrafish
- Authors
- Katsouda, A., Peleli, M., Asimakopoulou, A., Papapetropoulos, A., Beis, D.
- ID
- ZDB-PUB-200225-2
- Date
- 2020
- Source
- Biomolecules 10(2): (Journal)
- Registered Authors
- Beis, Dimitris
- Keywords
- 3-mercaptopyruvate sulfurtransferase, hydrogen sulfide, reactive oxygen species, zebrafish
- MeSH Terms
-
- Animals
- CRISPR-Cas Systems*
- Hydrogen Sulfide/metabolism
- Oxidative Stress*
- Regeneration
- Sulfurtransferases/genetics*
- Sulfurtransferases/metabolism
- Zebrafish/embryology
- Zebrafish/genetics*
- Zebrafish/physiology
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- PubMed
- 32079278 Full text @ Biomolecules
Citation
Katsouda, A., Peleli, M., Asimakopoulou, A., Papapetropoulos, A., Beis, D. (2020) Generation and Characterization of a CRISPR/Cas9 -Induced 3-mst Deficient Zebrafish. Biomolecules. 10(2):.
Abstract
3-mercaptopyruvate sulfurtransferase (3-MST) is an enzyme capable of synthesizing hydrogen sulfide (H2S) and polysulfides. In spite of its ubiquitous presence in mammalian cells, very few studies have investigated its contribution to homeostasis and disease development, thus the role of 3-MST remains largely unexplored. Here, we present a clustered, regularly interspaced, short palindromic repeats (CRISPR)/CRISPR-associated protein-9 (Cas9) induced 3-mst mutant zebrafish line, which will allow the study of 3-MST's role in several biological processes. The 3-mst zebrafish orthologue was identified using a bioinformatic approach and verified by its ability to produce H2S in the presence of 3-mercaptopyruvate (3-MP). Its expression pattern was analyzed during zebrafish early development, indicating predominantly an expression in the heart and central nervous system. As expected, no detectable levels of 3-Mst protein were observed in homozygous mutant larvae. In line with this, H2S levels were reduced in 3-mst-/- zebrafish. Although the mutants showed no obvious morphological deficiencies, they exhibited increased lethality under oxidative stress conditions. The elevated levels of reactive oxygen species, detected following 3-mst deletion, are likely to drive this phenotype. In line with the increased ROS, we observed accelerated fin regenerative capacity in 3-mst deficient zebrafish. Overall, we provide evidence for the expression of 3-mst in zebrafish, confirm its important role in redox homeostasis and indicate the enzyme's possible involvement in the regeneration processes.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping