The Role of DNA Methylation Reprogramming During Sex Determination and Transition in Zebrafish
- Author:
Wang XINXIN
1
,
2
;
Ma XIN
;
Wei GAOBO
;
Ma WEIRUI
;
Zhang ZHEN
;
Chen XUEPENG
;
Gao LEI
;
Liu ZHENBO
;
Yuan YUE
;
Yi LIZHI
;
Wang JUN
;
Tokumoto TOSHINOBU
;
Huang JUNJIU
;
Chen DAHUA
;
Zhang JIAN
;
Liu JIANG
Author Information
1. CAS Key Laboratory of Genome Sciences and Information,Beijing Institute of Genomics,Chinese Academy of Sciences/China National Center for Bioinformation,Beijing 100101,China
2. University of Chinese Academy of Sciences,Beijing 100049,China
- Keywords:
Germ cell;
DNA methylation;
Sex determination;
Sex transition;
Sexual plasticity
- From:
Genomics, Proteomics & Bioinformatics
2021;19(1):48-63
- CountryChina
- Language:Chinese
-
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 reveal that primordial germ cells (PGCs) undergo significant DNA methylation reprogramming during germ cell development, and the methylome of PGCs is reset 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 DNMT activity can prevent the female-to-male sex transition, sug-gesting that methylation reprogramming is required for zebrafish sex transition. In summary, DNA methylation plays important roles in zebrafish germ cell development and sexual plasticity.