PUBLICATION
Disruption of integrin α4 in zebrafish leads to cephalic hemorrhage during development
- Authors
- Iida, A., Wang, Z., Sehara-Fujisawa, A.
- ID
- ZDB-PUB-191005-5
- Date
- 2019
- Source
- Genes & genetic systems 94(4): 177-179 (Journal)
- Registered Authors
- Sehara-Fujisawa, Atsuko
- Keywords
- genome editing, hemorrhage, integrin α4, zebrafish
- MeSH Terms
-
- Animals
- CRISPR-Cas Systems/genetics
- Cell Communication/genetics
- Embryonic Development/genetics*
- Gene Editing
- Gene Expression Regulation, Developmental/genetics
- Genome/genetics
- Head/growth & development
- Head/pathology
- Hemorrhage/physiopathology
- Heterozygote
- Integrin alpha4/genetics*
- Morphogenesis/genetics*
- Phenotype
- Zebrafish/genetics*
- Zebrafish/growth & development
- PubMed
- 31582646 Full text @ Genes Genet. Sys.
Citation
Iida, A., Wang, Z., Sehara-Fujisawa, A. (2019) Disruption of integrin α4 in zebrafish leads to cephalic hemorrhage during development. Genes & genetic systems. 94(4):177-179.
Abstract
Integrins, transmembrane molecules that facilitate cell-to-cell and cell-to-extracellular matrix interactions, are heterodimers that consist of an α- and β-subunit. The integrin α4 gene (itgα4) is expressed in various type of cells and tissues. Its biochemical functions and physiological roles have been revealed using cultured cell assays. In contrast, the primary effect caused by itgα4 deletion on vertebrate development is poorly understood, because knockout mice exhibit multiple defects that can lead to embryonic lethality in the uterus. Zebrafish are a convenient vertebrate model to investigate morphogenesis during embryogenesis, because of their external fertilization and subsequent development outside the female's body. Here, we generated a zebrafish mutant line named itgα4 ko108 using the CRISPR/Cas9 genome editing system; the mutant genome harbored an approximately 2.0-kb deletion in the itgα4 locus. A truncated transcript was detected in itgα4 (+/-) or (-/-) fish but not in (+/+) fish. The mutant transcript was hypothesized to encode a truncated Itgα4 protein due to a premature stop codon. itgα4 (-/-) embryos obtained from the mating of heterozygous parents exhibited no apparent phenotype during development at 24 hours post-fertilization (hpf). However, approximately half of them exhibited cephalic hemorrhage at 48 hpf. The incidence ratio was significantly higher than that in (+/+) or (+/-) embryos. Embryonic hemorrhage has also been reported previously in Itgα4 knockout mice. In contrast, embryonic lethality with the other defects reported in the knockout mice was not observed in our zebrafish model. Therefore, the mutant line itgα4 ko108 should be a useful model to investigate a physiological function for Itgα4 in the blood circulation system.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping