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PRDM14 and BLIMP1 control the development of chicken primordial germ cells
Yuya Okuzaki1, Hidenori Kaneoka1, Takayuki Suzuki2
1Department of Biomolecular Engineering, Graduate School of Engineering, Furo-cho, Chikusa-ku, Nagoya, 464-8603, Japan.
Insights
Chicken PRDM14 and BLIMP1 are crucial for primordial germ cell (PGC) development and self-renewal. Knockdown of these genes reduced PGC numbers, indicating their essential roles in early embryonic development.
Area of Science:
- Developmental Biology
- Cell Biology
- Genetics
Background:
- Primordial germ cell (PGC) specification is vital for reproduction.
- PR domain-containing protein 14 (PRDM14) and B lymphocyte-induced maturation protein 1 (BLIMP1) are key regulators in mouse PGCs.
Purpose of the Study:
- To investigate the roles of chicken PRDM14 and BLIMP1 orthologs in PGC development.
- To elucidate the regulatory pathways controlling PGC specification in avian embryos.
Main Methods:
- Expression analysis of PRDM14 and BLIMP1 in chicken blastodermal cells and PGCs.
- In vivo knockdown using replication-competent retroviral vectors expressing shRNAs.
- Inhibition of signaling pathways (Activin, MEK) in cultured PGCs.
Main Results:
- PRDM14 and BLIMP1 are expressed in chicken blastodermal cells and PGCs.
- Knockdown of PRDM14 or BLIMP1 significantly reduced the number of SSEA-1 and chicken vasa homologue-positive PGCs.
- Activin A and FGF2 signaling pathways appear to regulate PRDM14, BLIMP1, and NANOG expression.
Conclusions:
- Chicken PRDM14 and BLIMP1 are essential for PGC development and maintenance.
- NANOG, PRDM14, and BLIMP1 are involved in PGC self-renewal in both cultured cells and embryos.
- Activin and FGF signaling pathways play a regulatory role in avian PGC development.
Abstract:
The differentiation of primordial germ cells (PGCs) is a fundamental step in development. PR domain-containing protein 14 (PRDM14) and B lymphocyte-induced maturation protein 1 (BLIMP1) play pivotal roles in mouse PGC specification. In the present study, we assessed the roles of chicken orthologs of PRDM14 and BLIMP1 in PGC development. PRDM14 and BLIMP1 were expressed in blastodermal cells and PGCs. The in vivo knockdown of PRDM14 or BLIMP1 by introducing a replication-competent retroviral vector expressing shRNAs to the blastodermal stage of embryos reduced the number of SSEA-1 or chicken vasa homologue-positive PGCs on day 5.5-6.5. Since the inhibition of Activin receptor-like kinase 4/5/7 in cultured PGCs reduced the expression of PRDM14, BLIMP1, and NANOG, and that of MEK inhibited PRDM14 expression, the expression of these genes seems to be controlled by Activin A and FGF2 signaling. Overall, PRDM14, BLIMP1, and NANOG seem to be involved in the self-renewal of PGCs in cultured PGCs and embryos.
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