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EBNA3蛋白的协同功能对于EB病毒的持续存在和潜伏至关重要。

The Cooperative Functions of the EBNA3 Proteins Are Central to EBV Persistence and Latency.

作者信息

Styles Christine T, Paschos Kostas, White Robert E, Farrell Paul J

机构信息

Molecular Virology, Department of Medicine, Imperial College London, London W2 1PG, UK.

出版信息

Pathogens. 2018 Mar 17;7(1):31. doi: 10.3390/pathogens7010031.

Abstract

The Epstein-Barr nuclear antigen 3 (EBNA3) family of proteins, comprising EBNA3A, EBNA3B, and EBNA3C, play pivotal roles in the asymptomatic persistence and life-long latency of Epstein-Barr virus (EBV) in the worldwide human population. EBNA3-mediated transcriptional reprogramming of numerous host cell genes promotes in vitro B cell transformation and EBV persistence in vivo. Despite structural and sequence similarities, and evidence of substantial cooperative activity between the EBNA3 proteins, they perform quite different, often opposing functions. Both EBNA3A and EBNA3C are involved in the repression of important tumour suppressive pathways and are considered oncogenic. In contrast, EBNA3B exhibits tumour suppressive functions. This review focuses on how the EBNA3 proteins achieve the delicate balance required to support EBV persistence and latency, with emphasis on the contribution of the Allday laboratory to the field of EBNA3 biology.

摘要

爱泼斯坦-巴尔核抗原3(EBNA3)蛋白家族由EBNA3A、EBNA3B和EBNA3C组成,在全球人类群体中,该蛋白家族在爱泼斯坦-巴尔病毒(EBV)的无症状持续存在和终身潜伏中发挥着关键作用。EBNA3介导的众多宿主细胞基因的转录重编程促进了体外B细胞转化以及EBV在体内的持续存在。尽管EBNA3蛋白之间存在结构和序列相似性,并且有证据表明它们之间存在大量协同活性,但它们执行的功能却截然不同,且常常相互对立。EBNA3A和EBNA3C都参与重要肿瘤抑制途径的抑制,被认为具有致癌性。相比之下,EBNA3B具有肿瘤抑制功能。本综述重点关注EBNA3蛋白如何实现支持EBV持续存在和潜伏所需的微妙平衡,同时着重介绍奥尔迪实验室对EBNA3生物学领域的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7563/5874757/6061b317d7c0/pathogens-07-00031-g001.jpg

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