PUBLICATION
Maternal miR-202-5p is required for zebrafish primordial germ cell migration by protecting small GTPase Cdc42
- Authors
- Jin, Y., Liu, W., Xiang, Y., Zhang, W., Zhang, H., Jia, K., Yi, M.
- ID
- ZDB-PUB-191120-8
- Date
- 2019
- Source
- Journal of molecular cell biology 12(7): 530-542 (Journal)
- Registered Authors
- Keywords
- Cdc42, Cdc42se1, miR-202-5p, migration, primordial germ cell
- MeSH Terms
-
- Animals
- Base Sequence
- Cell Movement/genetics*
- Female
- Fertility/genetics
- Gene Expression Regulation, Developmental
- Germ Cells/cytology*
- Germ Cells/metabolism*
- MicroRNAs/genetics
- MicroRNAs/metabolism*
- Mutation/genetics
- Zebrafish/genetics
- Zebrafish/metabolism*
- cdc42 GTP-Binding Protein/metabolism*
- PubMed
- 31742346 Full text @ J. Mol. Cell Biol.
Citation
Jin, Y., Liu, W., Xiang, Y., Zhang, W., Zhang, H., Jia, K., Yi, M. (2019) Maternal miR-202-5p is required for zebrafish primordial germ cell migration by protecting small GTPase Cdc42. Journal of molecular cell biology. 12(7):530-542.
Abstract
In many lower animals, germ cell formation, migration and maintenance depend on maternally provided determinants in germ plasm. In zebrafish, these processes have been extensively studied in terms of RNA binding proteins and other coding genes. The role of small non-coding RNAs in the regulation of primordial germ cell (PGC) development remains largely unknown and poorly investigated, even though growing interests for the importance of miRNAs involved in a wide variety of biological processes. Here, we reported the role and mechanism of the germ plasm-specific miRNA miR-202-5p in PGC migration; (i) both maternal loss and knockdown of miR-202-5p impaired PGC migration indicated by the mislocalization and reduced number of PGCs, (ii) cdc42se1 was a direct target gene of miR-202-5p, and overexpression of Cdc42se1 in PGCs caused PGC migration defects similar to those observed in loss of miR-202-5p mutants; (iii) Cdc42se1 not only interacted with Cdc42, but also inhibited cdc42 transcription, and overexpression of Cdc42 could rescue PGC migration defects in Cdc42se1 overexpressed embryos. Thus, miR-202-5p regulates PGC migration by directly targeting and repressing Cdc42se1 to protect the expression of Cdc42, which interacts with Actin to direct PGC migration.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping