PUBLICATION
Visualization of Turbot (Scophthalmus maximus) Primordial Germ Cells in vivo Using Fluorescent Protein Mediated by the 3' Untranslated Region of nanos3 or vasa Gene
- Authors
- Zhou, L., Wang, X., Liu, Q., Xu, S., Zhao, H., Han, M., Wang, Y., Song, Z., Li, J.
- ID
- ZDB-PUB-190911-6
- Date
- 2019
- Source
- Marine biotechnology (New York, N.Y.) 21(5): 671-682 (Journal)
- Registered Authors
- Keywords
- Location, Primordial germ cells, Scophthalmus maximus, nanos3, vasa
- MeSH Terms
-
- Cell Tracking/methods*
- Microinjections
- RNA-Binding Proteins/genetics
- RNA-Binding Proteins/metabolism
- Base Sequence
- Zygote
- Luminescent Proteins/genetics
- Luminescent Proteins/metabolism
- Nucleic Acid Conformation
- Germ Cells/cytology
- Germ Cells/growth & development
- Germ Cells/metabolism*
- Species Specificity
- Fish Proteins/genetics*
- Fish Proteins/metabolism
- Sequence Alignment
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism
- Oryzias/genetics
- Oryzias/growth & development
- Oryzias/metabolism
- Sequence Homology, Nucleic Acid
- Flatfishes/genetics*
- Flatfishes/growth & development
- Flatfishes/metabolism
- 3' Untranslated Regions
- Genes, Reporter
- Animals
- Recombinant Fusion Proteins/genetics*
- Recombinant Fusion Proteins/metabolism
- Zebrafish/genetics*
- Zebrafish/growth & development
- Zebrafish/metabolism
- DEAD-box RNA Helicases/genetics
- DEAD-box RNA Helicases/metabolism
- PubMed
- 31502176 Full text @ Mar. Biotechnol.
Citation
Zhou, L., Wang, X., Liu, Q., Xu, S., Zhao, H., Han, M., Wang, Y., Song, Z., Li, J. (2019) Visualization of Turbot (Scophthalmus maximus) Primordial Germ Cells in vivo Using Fluorescent Protein Mediated by the 3' Untranslated Region of nanos3 or vasa Gene. Marine biotechnology (New York, N.Y.). 21(5):671-682.
Abstract
Primordial germ cells (PGCs) as the precursors of germ cells are responsible for transmitting genetic information to the next generation. Visualization of teleost PGCs in vivo is essential to research the origination and development of germ cells and facilitate further manipulation on PGCs isolation, cryopreservation, and surrogate breeding. In this study, artificially synthesized mRNAs constructed by fusing fluorescent protein coding region to the 3' untranslated region (3'UTR) of nanos3 or vasa (mCherry-Smnanos3 3'UTR or mCherry-Smvasa 3'UTR mRNA) were injected into turbot (Scophthalmus maximus) fertilized eggs for tracing PGCs. The results demonstrated that the fluorescent PGCs differentiated from somatic cells and aligned on both sides of the trunk at the early segmentation period, then migrated and located at the dorsal part of the gut where the gonad would form. In the same way, we also found that the zebrafish (Danio rerio) vasa 3'UTR could trace turbot PGCs, while the vasa 3'UTR s of marine medaka (Oryzias melastigma) and red seabream (Pagrus major) failed, although they could label the marine medaka PGCs. In addition, through comparative analysis, we discovered that some potential sequence elements in the3 'UTRs of nanos3 and vasa, such as GCACs, 62-bp U-rich regions and nucleotide 187-218 regions might be involved in PGCs stabilization. The results of this study provided an efficient, rapid, and specific non-transgenic approach for visualizing PGCs of economical marine fish in vivo.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping