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1.
Gen Comp Endocrinol ; 277: 56-65, 2019 06 01.
Article in English | MEDLINE | ID: mdl-30878349

ABSTRACT

Unlike its paralog Foxl2, which is well known for its role in ovarian development in vertebrates, the function of Foxl3 is still unclear. Foxl3 is an ancient duplicated copy of Foxl2. It is present as a single copy in ray-finned fish. But, due to repeated losses, it is absent in most tetrapods. Our transcriptomic data, however, show that two Foxl3s (Foxl3a and its paralog Foxl3b) are present in Japanese eel. Foxl3a is predominantly expressed in the pituitary, and Foxl3b is predominantly expressed in the gills. Both Foxl3s show a sex-dimorphic expression, being higher expression in testes than in ovaries. Moreover, Foxl3a and Foxl3b were exclusively expressed during gonadal differentiation in control eels (100% male). Conversely, Foxl3a and Foxl3b significantly decreased after gonadal differentiation in E2-treated eels (100% female). Furthermore, in accordance the difference in adhesive ability between somatic cells and germline cells in testes, Foxl3s showed a high expression in suspension cells (putative germline cells) and low expression in adhesive cells (putative somatic cells). In situ hybridization further showed that Foxl3a and Foxl3b were expressed in the testicular germline cells. In addition, Foxl3s expression was not changed by sex steroids in in vitro testes culture. Taken together, our results suggest that the teleost-specific Foxl3 paralog was repeatedly lost in most fish after the third round of whole genome duplication. The two germline-expressed Foxl3s had higher expression levels in males than in females during gonadal differentiation in Japanese eel. These results demonstrated that Foxl3s might play an important role in germline sexual fate determination from ancient fish to modern fish.


Subject(s)
Anguilla/genetics , Anguilla/physiology , Forkhead Transcription Factors/genetics , Gene Expression Regulation, Developmental , Germ Cells/metabolism , Gonads/physiology , Sex Differentiation/physiology , Amino Acid Sequence , Animals , Body Size/drug effects , Estradiol/pharmacology , Forkhead Transcription Factors/chemistry , Forkhead Transcription Factors/metabolism , Gene Expression Profiling , Gene Expression Regulation, Developmental/drug effects , Germ Cells/drug effects , Gonads/drug effects , Male , Phylogeny , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sex Differentiation/drug effects , Sex Differentiation/genetics , Steroids/pharmacology , Testis/cytology , Testis/drug effects , Testis/metabolism
2.
Biol Reprod ; 99(5): 1034-1044, 2018 11 01.
Article in English | MEDLINE | ID: mdl-29901793

ABSTRACT

Unlike vitellogenin, which is the sole major precursor of yolk protein in all oviparous vertebrates, a variety of major precursor of yolk proteins are found among oviparous invertebrates. Sea urchins have a transferrin-like yolk protein, while all other major precursors of yolk proteins in oviparous invertebrates belong to the superfamily of large lipid transfer proteins (LLTPs). However, a comprehensive understanding of vitellogenesis is absent in cephalopods. To understand control of vitellogenesis by the LLTPs gene, two vitellogenins (VTG1 and VTG2), two apolipophorins (APOLP2A and APOLP2B), and a cytosolic large subunit of microsomal triglyceride transfer protein (MTTP) found in the bigfin reef squid. Only the two VTGs showed high levels of expression in mature females compared to males. We further analyzed the expression profile and localization of both VTGs/VTGs during ovarian development. Our data showed that VTGs/VTGs expressions were correlated to the female reproductive cycle. Ovarian VTG1 and VTG2 were localized in the follicle cells but not in oocytes. In addition, VTG1 and VTG2 were represented in follicle cells and oocytes. Thus, our results showed that both VTGs were synthesized by follicle cells and are then delivered to oocytes. In addition, we demonstrated that VTGs were the major precursor of yolk protein in bigfin reef squid. We also found differential proteolytic cleavage processes of VTG1 and VTG2 during VTGs accumulation in oocytes. Therefore, our data shed light on the molecular mechanism of the yolk accumulation pathway in cephalopods.


Subject(s)
Decapodiformes/genetics , Gene Expression Regulation, Developmental/genetics , Vitellogenins/genetics , Animals , Egg Proteins/biosynthesis , Egg Proteins/genetics , Embryonic Development/genetics , Female , Male , Oocytes/metabolism , Ovarian Follicle/metabolism , Ovary/metabolism , Reproduction/genetics , Reproduction/physiology , Sex Characteristics
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