Germline development in rat revealed by visualization and deletion of Prdm14

Author:

Kobayashi Toshihiro12ORCID,Kobayashi Hisato3ORCID,Goto Teppei1ORCID,Takashima Tomoya4,Oikawa Mami1,Ikeda Hiroki3,Terada Reiko1,Yoshida Fumika1,Sanbo Makoto1,Nakauchi Hiromitsu56,Kurimoto Kazuki3,Hirabayashi Masumi12ORCID

Affiliation:

1. Center for Genetic Analysis of Behavior, National Institute for Physiological Sciences, Okazaki, 444-8787, Aichi, Japan

2. The Graduate University of Advanced Studies, Okazaki, 444-8787, Aichi, Japan

3. Department of Embryology, Nara Medical University, Kashihara, 634-0813, Nara, Japan

4. Department of Bioscience, Tokyo University of Agriculture, Setagaya-ku, 156-8502, Tokyo, Japan

5. Division of Stem Cell Therapy, Institute of Medical Science, The University of Tokyo, Minato-ku, 108-8639, Tokyo, Japan

6. Institute for Stem Cell Biology and Regenerative Medicine, Department of Genetics, Stanford University School of Medicine, Stanford, CA, 94305, USA

Abstract

Primordial germ cells (PGCs), the founder cells of the germline, are specified in pre-gastrulating embryos in mammals, and subsequently migrate towards gonads to mature into functional gametes. Here, we investigated PGC development in rats, by genetically modifying Prdm14, a unique marker and a critical PGC transcriptional regulator. We trace PGC development in rats, for the first time, from specification until sex determination stage in fetal gonads using Prdm14 H2BVenus knock-in rats. We uncover that Prdm14’s crucial role in PGC specification is conserved between rat and mice, by analyzing Prdm14 deficient rat embryos. Notably, loss of Prdm14 completely abrogates the PGC program: failure in maintenance and/or activation of germ cell markers and pluripotency genes. Finally, we profile the transcriptome of the postimplantation epiblast and all PGC stages in rat, to reveal enrichment of distinct gene sets at each transition point, thereby providing an accurate transcriptional time-line for rat PGC development. Thus, the novel genetically modified rats and data sets obtained in this study will advance our knowledge on conserved vs species-specific features for germline development in mammals.

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

Reference54 articles.

1. Progress and prospects in rat genetics: a community view;Aitman;Nat. Genet.,2008

2. A mesodermal factor, T, specifies mouse germ cell fate by directly activating germline determinants;Aramaki;Dev. Cell,2013

3. A quantitative study of primordial germ cells in the male rat;Beaumont;J. Embryol. Exp. Morphol.,1963

4. Transcriptional and epigenetic control of germline competence and specification;Bleckwehl;Curr. Opin. Cell Biol.,2019

5. Rapid loss of Oct-4 and pluripotency in cultured rodent blastocysts and derivative cell lines;Buehr;Biol. Reprod.,2003

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