PUBLICATION
Generation of germ-line chimera zebrafish using primordial germ cells isolated from cultured blastomeres and cryopreserved embryoids
- Authors
- Kawakami, Y., Goto-Kazeto, R., Saito, T., Fujimoto, T., Higaki, S., Takahashi, Y., Arai, K., and Yamaha, E.
- ID
- ZDB-PUB-110214-18
- Date
- 2010
- Source
- The International journal of developmental biology 54(10): 1493-1501 (Journal)
- Registered Authors
- Keywords
- germ-line chimera, primordial germ cell, cryopreservation, dissociated blastomere
- MeSH Terms
-
- Animals
- Transplantation
- RNA-Binding Proteins
- Zebrafish Proteins/genetics
- Cell Movement
- Embryo, Nonmammalian/cytology
- Embryoid Bodies/cytology*
- Embryoid Bodies/transplantation*
- Cryopreservation
- Gonads
- Zebrafish
- Cells, Cultured/cytology
- Germ Cells/cytology*
- Germ Cells/transplantation*
- RNA, Messenger
- Blastomeres/cytology*
- Blastomeres/transplantation
- Chimera*
- Green Fluorescent Proteins
- Blastula/cytology
- Blastula/embryology
- Blastula/transplantation
- 3' Untranslated Regions
- Staining and Labeling
- PubMed
- 21302258 Full text @ Int. J. Dev. Biol.
Citation
Kawakami, Y., Goto-Kazeto, R., Saito, T., Fujimoto, T., Higaki, S., Takahashi, Y., Arai, K., and Yamaha, E. (2010) Generation of germ-line chimera zebrafish using primordial germ cells isolated from cultured blastomeres and cryopreserved embryoids. The International journal of developmental biology. 54(10):1493-1501.
Abstract
Primordial germ cells (PGCs) are the only cells in developing embryos with the potential to transmit genetic information to the next generation. In our previous study, a single PGC transplanted into a host differentiated into fertile gametes and produced germ-line chimeras of cyprinid fish, including zebrafish. In this study, we aimed to induce germ-line chimeras by transplanting donor PGCs from various sources (normal embryos at different stages, dissociated blastomeres, embryoids, or embryoids cryopreserved by vitrification) into host blastulae, and compare the migration rates of the PGCs towards the gonadal ridge. Isolated, cultured blastomeres not subject to mesodermal induction were able to differentiate into PGCs that retained their motility. Moreover, these PGCs successfully migrated towards the gonadal ridge of the host and formed viable gametes. Motility depended on developmental stage and culture duration: PGCs obtained at earlier developmental stages and with shorter cultivation periods showed an increased rate of migration to the gonadal ridge. Offspring were obtained from natural spawning between normal females and chimeric males. These results provide the basis for new methods of gene preservation in zebrafish.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping