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斑马鱼Nedd8通过抑制雄激素受体活性促进卵巢发育和维持雌性第二性征。

Zebrafish Nedd8 facilitates ovarian development and the maintenance of female secondary sexual characteristics via suppression of androgen receptor activity.

作者信息

Yu Guangqing, Liu Xing, Zhang Dawei, Wang Jing, Ouyang Gang, Chen Zhu, Xiao Wuhan

机构信息

State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, P. R. China.

Department of Fisheries, University of Chinese Academy of Sciences, Beijing, 100049, Wuhan, 430072, P. R. China.

出版信息

Development. 2020 Sep 25;147(18):dev194886. doi: 10.1242/dev.194886.

Abstract

Nedd8 is a ubiquitin-like protein that covalently conjugates to target proteins through neddylation. In addition to cullin-RING ligases, neddylation also modifies non-cullin proteins to regulate protein activity, stability and localization. However, the roles of remain largely unknown Here, we found that loss of in female zebrafish led to defects in oogenesis, disrupted oocyte maturation and stimulated growth of the breeding tubercles (BTs) on the pectoral fins. The BTs are normally present in males, not females. However, the loss of one copy of can partially rescue the phenotypes displayed by -null female zebrafish. Further assays indicated that Nedd8 conjugates to Ar and Ar is neddylated at lysine 475 and lysine 862. Moreover, Nedd8 conjugation efficiently suppressed Ar transcriptional activity. Lysine 862 (K862) of Ar is the key site modified by neddylation to modulate Ar transcriptional activity. Thus, our results not only demonstrated that Nedd8 modulates ovarian maturation and the maintenance of female secondary sexual characteristics of female zebrafish , but also indicated that androgen signaling is strictly regulated by .

摘要

Nedd8是一种类泛素蛋白,通过Neddylation共价结合到靶蛋白上。除了cullin-RING连接酶外,Neddylation还修饰非cullin蛋白以调节蛋白活性、稳定性和定位。然而,其作用在很大程度上仍不清楚。在这里,我们发现雌性斑马鱼中该蛋白缺失导致卵子发生缺陷、卵母细胞成熟受阻,并刺激胸鳍上繁殖瘤(BTs)的生长。BTs通常存在于雄性而非雌性中。然而,该蛋白一个拷贝的缺失可部分挽救该蛋白缺失的雌性斑马鱼所表现出的表型。进一步的实验表明,Nedd8与雄激素受体(Ar)结合,且Ar在赖氨酸475和赖氨酸862处发生Neddylation修饰。此外,Nedd8结合有效地抑制了Ar的转录活性。Ar的赖氨酸862(K862)是Neddylation修饰以调节Ar转录活性的关键位点。因此,我们的结果不仅证明了Nedd8调节雌性斑马鱼的卵巢成熟和雌性第二性征的维持,还表明雄激素信号通路受到该蛋白的严格调控。

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