Porcine epidemic diarrhea virus E protein induces formation of stress granules and attenuates protein translation through activation of the PERK/eIF2α signaling pathway

猪流行性腹泻病毒 生物 未折叠蛋白反应 蛋白质生物合成 内质网 蛋白激酶R 翻译(生物学) 病毒学 病毒 eIF2 真核生物γ翻译起始因子4 细胞生物学 磷酸化 分子生物学 蛋白激酶A 遗传学 信使核糖核酸 细胞周期蛋白依赖激酶2 基因
作者
Liang Zheng,Ying Yang,Yifeng Han,Jiawen Yu,Zhijun Wu,Matthew Kay,Wenlong Xia,Zhibao Chen,Jinzhu Ma,Xiaoge Yang,Liwei Yin,Xiaojuan Xu,Hua Zhang
出处
期刊:Veterinary Microbiology [Elsevier BV]
卷期号:293: 110095-110095 被引量:8
标识
DOI:10.1016/j.vetmic.2024.110095
摘要

Porcine epidemic diarrhea virus (PEDV) envelope protein (E) has been characterized as an important structural protein that plays critical roles in the interplay with its host to affect the virus life cycle. Stress granules (SGs) are host translationally silent ribonucleoproteins, which are mainly induced by the phosphorylation of eIF2α in the PERK/eIF2α signaling pathway. Our previous study found that PEDV E protein caused endoplasmic reticulum stress response (ERS)-mediated suppression of antiviral proteins' translation. However, the link and the underlying mechanism by which PEDV induces SGs formation and suppresses host translation remain elusive. In this study, our results showed that PEDV E protein significantly elevated the expression of GRP78, CANX, and phosphorylation of PERK and eIF2α, indicating that the PERK/eIF2α branch of ERS was activated. PEDV E protein localized to the ER and aggregated into puncta to reconstruct ER structure, and further induced SGs formation, which has been caused through upregulating the G3BP1 expression level. In addition, a significant global translational stall and endogenous protein translation attenuation were detected in the presence of E protein overexpression, but the global mRNA transcriptional level remained unchanged, suggesting that the shutoff of protein translation was associated with the translation, not with the transcription process. Collectively, this study demonstrates that PERK/eIF2α activation is required for SGs formation and protein translation stall. This study is beneficial for us to better understand the mechanism by which PEDV E suppresses host protein synthesis, and provides us a new insight into the host translation regulation during virus infection.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
Monica发布了新的文献求助10
1秒前
3秒前
丹牛完成签到,获得积分10
3秒前
Wzebrafish发布了新的文献求助10
4秒前
1y发布了新的文献求助10
4秒前
在水一方应助mildjorker采纳,获得10
5秒前
XLL关闭了XLL文献求助
5秒前
文静老三完成签到,获得积分20
5秒前
7秒前
等候完成签到 ,获得积分10
7秒前
陈平安发布了新的文献求助10
8秒前
略微妙蛙完成签到 ,获得积分10
8秒前
9秒前
9秒前
loii举报坦率的犀牛求助涉嫌违规
10秒前
yang完成签到,获得积分10
10秒前
fmm发布了新的文献求助10
11秒前
欧阳蛋蛋鸡完成签到 ,获得积分10
11秒前
大力的图图应助StoneT采纳,获得10
11秒前
赘婿应助科研通管家采纳,获得10
12秒前
Orange应助科研通管家采纳,获得10
12秒前
12秒前
天天快乐应助科研通管家采纳,获得10
12秒前
充电宝应助科研通管家采纳,获得10
12秒前
12秒前
12秒前
12秒前
12秒前
斯文败类应助科研通管家采纳,获得10
12秒前
12秒前
SciGPT应助科研通管家采纳,获得10
12秒前
eggwu发布了新的文献求助10
12秒前
香蕉觅云应助科研通管家采纳,获得10
13秒前
思源应助科研通管家采纳,获得10
13秒前
13秒前
英俊的铭应助科研通管家采纳,获得10
13秒前
syhero发布了新的文献求助10
14秒前
沉静的万天完成签到,获得积分10
14秒前
14秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
Signals, Systems, and Signal Processing 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Research Methods for Applied Linguistics 500
Picture Books with Same-sex Parented Families Unintentional Censorship 444
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6413325
求助须知:如何正确求助?哪些是违规求助? 8232272
关于积分的说明 17474264
捐赠科研通 5466019
什么是DOI,文献DOI怎么找? 2888153
邀请新用户注册赠送积分活动 1864840
关于科研通互助平台的介绍 1703108