| Literature DB >> 33610791 |
Xinxin Wang1, Xin Ma1, Gaobo Wei2, Weirui Ma3, Zhen Zhang4, Xuepeng Chen5, Lei Gao5, Zhenbo Liu5, Yue Yuan3, Lizhi Yi1, Jun Wang6, Toshinobu Tokumoto6, Junjiu Huang4, Dahua Chen7, Jian Zhang8, Jiang Liu9.
Abstract
DNA methylation is a prevalent epigenetic modification in vertebrates, and it has been shown to be involved the regulation of gene expression and embryo development. However, it remains unclear how DNA methylation regulates sexual development, especially in species without sex chromosomes. To determine this, we utilized zebrafish to investigate DNA methylation reprogramming during juvenile germ cell development and adult female-to-male sex transition. We revealed that primordial germ cells (PGCs) undergo significant DNA methylation reprogramming during germline development and set to an oocyte/ovary-like pattern at 9 days post fertilization (9 dpf). When DNA methyltransferase (DNMT) activity in juveniles was blocked after 9 dpf, the zebrafish developed into females. We also show that Tet3 is involved in PGC development. Notably, we find that DNA methylome reprogramming during adult zebrafish sex transition is similar to the reprogramming during the sex differentiation from 9 dpf PGCs to sperm. Furthermore, inhibiting DNMTs activity can prevent the female-to-male sex transition, suggesting that methylation reprogramming is required for zebrafish sex transition. In summary, DNA methylation plays important roles in zebrafish germline development and sexual plasticity.Entities:
Keywords: DNA methylation; Germ cell; Sex determination; Sex transition; Sexual plasticity
Year: 2021 PMID: 33610791 DOI: 10.1016/j.gpb.2020.10.004
Source DB: PubMed Journal: Genomics Proteomics Bioinformatics ISSN: 1672-0229 Impact factor: 7.691