Reduced Vitellogenesis and Female Fertility in Gper Knockout Zebrafish

Xin Jun Wu, Marcus Jermaul Williams, Kimberly Ann Kew, Aubrey Converse, Peter Thomas, Yong Zhu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

The role G-protein coupled estrogen receptor (GPER) plays in vertebrate reproduction remains controversial. To investigate GPER’s reproductive role, we generated a gper zebrafish mutant line (gper−/−) using TALENs. Gper mutant females exhibited reduced fertility with a 40.85% decrease in embryo production which was associated with a significant decrease in the number of Stage V (730–750 μm) ovulated oocytes. Correspondingly, the number of early vitellogenic follicles (Stage III, 400–450 µm) in gper−/− ovaries was greater than that in wildtypes (wt), suggesting that subsequent follicle development was retarded in the gper−/− fish. Moreover, plasma vitellogenin levels were decreased in gper−/− females, and epidermal growth factor receptor (Egfr) expression was lower in Stage III vitellogenic oocytes than in wt counterparts. However, hepatic nuclear estrogen receptor levels were not altered, and estrogen levels were elevated in ovarian follicles. These results suggest that Gper is involved in the control of ovarian follicle development via regulation of vitellogenesis and Egfr expression in zebrafish.

Original languageEnglish (US)
Article number637691
JournalFrontiers in Endocrinology
Volume12
DOIs
StatePublished - Mar 9 2021

Funding

This work was supported by the NIH GM100461 to YZ.

Keywords

  • G-protein coupled estrogen receptor (Gper)
  • epidermal growth factor receptor (Egfr)
  • oocyte growth
  • reduced fertility
  • vitellogenin

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism

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