| Literature DB >> 28093265 |
Guijun Guan1, Kaiqing Sun2, Xi Zhang3, Xiaomiao Zhao4, Mingyou Li2, Yan Yan3, Yunzhi Wang3, Jianbin Chen3, Meisheng Yi5, Yunhan Hong3.
Abstract
Gonadal soma-derived factor (gsdf) is reported to be a male initiator in medaka based on loss- and gain- of function via targeted disruption, or transgenic over-expression. However, little is known about how gsdf promotes undifferentiated gonad entry into male pathways or prevents entry into the female pathway. We utilized a visible folliculogenesis system with a reporter cassette of dual-color fluorescence expression to identify difference between oocyte development from wildtype and gsdf deficiency medaka. A red fluorescent protein (RFP) is driven by a major component of the synaptonemal complex (SYCP3) promoter which enables RFP expression solely in oocytes after the onset of meiosis, and a histone 2b-EGFP fused protein (H2BEGFP) under the control of an elongation factor (EF1α) promoter, wildly used as a mitotic reporter of cell cycle. This mitosis-meiosis visible switch revealed that early meiotic oocytes present in gsdf deficiency were more than those in wildtype ovaries, corresponding to the decrease of inhibin expression detected by real-time qPCR analysis, suggesting gsdf is tightly involved in the process of medaka oocyte development at early stage.Entities:
Keywords: Folliculogenesis; Gonadal soma-derived factor (Gsdf); Meiosis; TGF-beta superfamily
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Year: 2017 PMID: 28093265 DOI: 10.1016/j.mod.2016.12.006
Source DB: PubMed Journal: Mech Dev ISSN: 0925-4773 Impact factor: 1.882