TY - JOUR
T1 - Reduced Vitellogenesis and Female Fertility in Gper Knockout Zebrafish
AU - Wu, Xin Jun
AU - Williams, Marcus Jermaul
AU - Kew, Kimberly Ann
AU - Converse, Aubrey
AU - Thomas, Peter
AU - Zhu, Yong
N1 - Funding Information:
This work was supported by the NIH GM100461 to YZ.
Publisher Copyright:
© Copyright © 2021 Wu, Williams, Kew, Converse, Thomas and Zhu.
PY - 2021/3/9
Y1 - 2021/3/9
N2 - 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.
AB - 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.
KW - G-protein coupled estrogen receptor (Gper)
KW - epidermal growth factor receptor (Egfr)
KW - oocyte growth
KW - reduced fertility
KW - vitellogenin
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U2 - 10.3389/fendo.2021.637691
DO - 10.3389/fendo.2021.637691
M3 - Article
C2 - 33790865
AN - SCOPUS:85102918057
SN - 1664-2392
VL - 12
JO - Frontiers in Endocrinology
JF - Frontiers in Endocrinology
M1 - 637691
ER -