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RNF146 E3泛素连接酶是非洲爪蟾中Wnt信号调控和身体模式形成所必需的。

The RNF146 E3 ubiquitin ligase is required for the control of Wnt signaling and body pattern formation in Xenopus.

作者信息

Zhu Xuechen, Xing Rui, Tan Renbo, Dai Rongyang, Tao Qinghua

机构信息

The Ministry of Education Key Laboratory in Protein Sciences, Tsinghua University School of Life Sciences, Beijing 100084, China.

Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences of Southwest Medical University, Luzhou, Sichuan 646000, China.

出版信息

Mech Dev. 2017 Oct;147:28-36. doi: 10.1016/j.mod.2017.08.001. Epub 2017 Aug 12.

DOI:10.1016/j.mod.2017.08.001
PMID:28807725
Abstract

The RING finger protein Rnf146 encodes an E3 ubiquitin ligase capable of targeting poly-ADP-ribosylated substrates for proteasomal degradation. Rnf146 has been identified as a critical regulator of Axin1 and thus of Wnt/β-catenin signaling. However its physiological significance in vertebrate embryonic development remains to be demonstrated. In this study, we take advantages of early Xenopus embryos to demonstrate that Rnf146 is essential for embryonic pattern formation. Depletion of zygotic Rnf146 using a translation blocking morpholino oligo (MO) results in anteriorized development and increased expression the anterior marker gene Otx2, consistent the notion that Rnf146 is a positive regulator of Wnt/β-catenin signaling through negatively regulating Axin1 expression. This notion is further supported by examination of the role of maternal Rnf146 in the context of Spemann organizer formation and dorsal axis development. Depletion of maternal Rnf146 using an antisense oligodeoxynucleic acid (ODN) leads to ventralized development and diminished expression of organizer genes. Together, we have provided evidence for the first time that Rnf146 is a critical regulator of embryonic pattern formation in vertebrates.

摘要

环状结构域蛋白Rnf146编码一种E3泛素连接酶,该酶能够将多聚ADP核糖基化的底物靶向蛋白酶体降解。Rnf146已被确定为Axin1的关键调节因子,因此也是Wnt/β-连环蛋白信号通路的关键调节因子。然而,其在脊椎动物胚胎发育中的生理意义仍有待证实。在本研究中,我们利用非洲爪蟾早期胚胎来证明Rnf146对胚胎模式形成至关重要。使用翻译阻断吗啉代寡核苷酸(MO)耗尽合子Rnf146会导致胚胎发育向前化,并增加前部标记基因Otx2的表达,这与Rnf146通过负向调节Axin1表达而成为Wnt/β-连环蛋白信号通路的正向调节因子这一观点一致。在斯佩曼组织者形成和背轴发育的背景下对母源Rnf146的作用进行研究,进一步支持了这一观点。使用反义寡脱氧核苷酸(ODN)耗尽母源Rnf146会导致胚胎发育向腹侧化,并减少组织者基因的表达。总之,我们首次提供了证据,证明Rnf146是脊椎动物胚胎模式形成的关键调节因子。

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