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FOXL2 down-regulates vitellogenin expression at mature stage in Eriocheir sinensis

机译:FOXL2下调中华绒螯蟹成熟阶段的卵黄蛋白原表达

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摘要

Ovarian development in crustaceans is characterized by rapid production of egg yolk protein in a process called vitellogenesis. In the present study, we investigated the involvement of a DEAD (Asp-Glu-Ala-Asp) box RNA helicase 20 (DDX20), forkhead transcription factor (FOXL)2 and fushi tarazu factor (FTZ-F)1 in the regulation of vitellogenesis. Based on ESTs from the testis and accessory gland of Eriocheir sinensis, we cloned the full-length cDNAs of foxl2 and fushitarazu factor 1 (ftz-f1), which include the conserved structural features of the forkhead family and nuclear receptor 5A (NR5A) family respectively. The expression of foxl2 mRNA surged at the mature stage of the ovary, when vtg mRNA swooped, suggesting that foxl2 negatively affects the vitellogenin (VTG) synthesis at this developmental stage. Etoposide (inducing germ cell apoptosis) treatment up-regulated FOXL2 and DDX20 at both the mRNA and the protein levels, primarily in the follicular cells as shown by immunofluorescence analysis. Furthermore, foxl2, ddx20 and ftz-f1 mRNA levels increased significantly with right-eyestalk ablation. Interactions between FOXL2 and DDX20 or FTZ-F1 were confirmed by co-immunoprecipitation and the forkhead domain of FOXL2 was identified as the specific structure interacting with FTZ-F1. In conclusion, FOXL2 down-regulates VTG expression by binding with DDX20 in regulation of follicular cell apoptosis and with FTZ-F1 to repress the synthesis of VTG at the mature stage. This report is the first to describe the molecular mechanism of VTG synthesis in E. sinensis and may shed new light on the regulation of cytochrome P450 enzyme by FOXL2 and FTZ-F1 in vitellogenesis.
机译:甲壳动物的卵巢发育的特征是在称为卵黄发生的过程中快速产生蛋黄蛋白。在本研究中,我们调查了DEAD(Asp-Glu-Ala-Asp)盒RNA解旋酶20(DDX20),叉头转录因子(FOXL)2和富士tarazu因子(FTZ-F)1的参与。卵黄发生。基于中华绒螯蟹睾丸和附属腺的EST,我们克隆了foxl2和fushitarazu因子1(ftz-f1)的全长cDNA,其中包括叉头家族和核受体5A(NR5A)家族的保守结构特征。分别。当vtg mRNA猛扑时,foxl2 mRNA的表达在卵巢成熟阶段激增,表明foxl2在此发育阶段对卵黄蛋白原(VTG)合成产生了负面影响。依托泊苷(诱导生殖细胞凋亡)治疗在mRNA和蛋白质水平(主要是在卵泡细胞中)上调FOXL2和DDX20的水平,如免疫荧光分析所示。此外,右眼柄消融后foxl2,ddx20和ftz-f1 mRNA水平显着增加。通过共免疫沉淀法证实了FOXL2与DDX20或FTZ-F1之间的相互作用,并且将FOXL2的叉头结构域鉴定为与FTZ-F1相互作用的特定结构。总之,FOXL2通过与DDX20结合来调节卵泡细胞凋亡并与FTZ-F1结合,从而下调VTG的表达,从而在成熟阶段抑制VTG的合成。该报告是第一个描述中华绒螯蟹VTG合成的分子机制,并可能为卵黄发生中FOXL2和FTZ-F1对细胞色素P450酶的调控提供新的启示。

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