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Blastocyst complementation using Prdm14-deficient rats enables efficient germline transmission and generation of functional mouse spermatids in rats.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Kobayashi, Toshihiro  ORCID logo  https://orcid.org/0000-0001-8019-0008
Goto, Teppei 
Oikawa, Mami 
Yoshida, Fumika 

Abstract

Murine animal models from genetically modified pluripotent stem cells (PSCs) are essential for functional genomics and biomedical research, which require germline transmission for the establishment of colonies. However, the quality of PSCs, and donor-host cell competition in chimeras often present strong barriers for germline transmission. Here, we report efficient germline transmission of recalcitrant PSCs via blastocyst complementation, a method to compensate for missing tissues or organs in genetically modified animals via blastocyst injection of PSCs. We show that blastocysts from germline-deficient Prdm14 knockout rats provide a niche for the development of gametes originating entirely from the donor PSCs without any detriment to somatic development. We demonstrate the potential of this approach by creating PSC-derived Pax2/Pax8 double mutant anephric rats, and rescuing germline transmission of a PSC carrying a mouse artificial chromosome. Furthermore, we generate mouse PSC-derived functional spermatids in rats, which provides a proof-of-principle for the generation of xenogenic gametes in vivo. We believe this approach will become a useful system for generating PSC-derived germ cells in the future.

Description

Keywords

Animals, Blastocyst, DNA-Binding Proteins, Embryonic Stem Cells, Female, Gene Knockout Techniques, Genetic Engineering, Germ Cells, Male, Mice, Models, Animal, Pluripotent Stem Cells, RNA-Binding Proteins, Rats, Spermatids, Transcription Factors, Transcriptome

Journal Title

Nat Commun

Conference Name

Journal ISSN

2041-1723
2041-1723

Volume Title

12

Publisher

Springer Science and Business Media LLC