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叉头框蛋白L2(FOXL2)在中华绒螯蟹成熟阶段下调卵黄蛋白原的表达。

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

作者信息

Li Qing, Xie Jing, He Lin, Wang Yuanli, Yang Hongdan, Duan Zelin, Wang Qun

机构信息

Laboratory of Immunological Defense & Reproduction, School of Life Science, East China Normal University, Shanghai 200241, China

Laboratory of Immunological Defense & Reproduction, School of Life Science, East China Normal University, Shanghai 200241, China.

出版信息

Biosci Rep. 2015 Oct 1;35(6):e00278. doi: 10.1042/BSR20150151.

DOI:10.1042/BSR20150151
PMID:26430246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4708011/
Abstract

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.

摘要

甲壳类动物的卵巢发育特征是在一个称为卵黄发生的过程中快速产生卵黄蛋白。在本研究中,我们调查了DEAD(天冬氨酸-谷氨酸-丙氨酸-天冬氨酸)盒RNA解旋酶20(DDX20)、叉头转录因子(FOXL)2和腹节缺失因子(FTZ-F)1在卵黄发生调控中的作用。基于中华绒螯蟹睾丸和附属腺的ESTs,我们克隆了foxl2和腹节缺失因子1(ftz-f1)的全长cDNA,它们分别包含叉头家族和核受体5A(NR5A)家族的保守结构特征。foxl2 mRNA的表达在卵巢成熟阶段激增,此时vtg mRNA急剧下降,这表明foxl2在这个发育阶段对卵黄蛋白原(VTG)的合成有负面影响。依托泊苷(诱导生殖细胞凋亡)处理在mRNA和蛋白质水平上均上调了FOXL2和DDX20,免疫荧光分析表明主要在卵泡细胞中上调。此外,foxl2、ddx20和ftz-f1 mRNA水平随着右眼柄切除而显著增加。通过免疫共沉淀证实了FOXL2与DDX20或FTZ-F1之间的相互作用,并且FOXL2的叉头结构域被确定为与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结合以在成熟阶段抑制VTG的合成,从而下调VTG表达。本报告首次描述了中华绒螯蟹VTG合成的分子机制,并可能为FOXL2和FTZ-F1在卵黄发生中对细胞色素P450酶的调控提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/03b59b6324d3/bsr035e278fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/1272cd87a324/bsr035e278fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/4169a47a0e9b/bsr035e278fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/d6d4e4939c44/bsr035e278fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/417c2c4cb49c/bsr035e278fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/24e1954f3cd7/bsr035e278fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/a3f6f073dbb2/bsr035e278fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/0192a24f84b7/bsr035e278fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/16c8df277ae3/bsr035e278fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/ba7434325be0/bsr035e278fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/03b59b6324d3/bsr035e278fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/1272cd87a324/bsr035e278fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/4169a47a0e9b/bsr035e278fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/d6d4e4939c44/bsr035e278fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/417c2c4cb49c/bsr035e278fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/24e1954f3cd7/bsr035e278fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/a3f6f073dbb2/bsr035e278fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/0192a24f84b7/bsr035e278fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/16c8df277ae3/bsr035e278fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/ba7434325be0/bsr035e278fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5631/4708011/03b59b6324d3/bsr035e278fig10.jpg

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