Rab14 regulates the transport of human papillomavirus to the trans-Golgi network for infectious cell entry

IF 3 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
FEBS Letters Pub Date : 2026-10-12 Epub Date: 2026-05-26 DOI:10.1002/1873-3468.70365
Yoshiyuki Ishii, Iwao Kukimoto
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引用次数: 0

Abstract

Human papillomavirus (HPV) utilizes multiple host proteins to infect epithelial cells. Here we identified Rab14, a small GTPase belonging to the Rab family, as a critical host factor in HPV infection. Rab14 knockout (KO) cells exhibited resistance to HPV pseudovirion (PsV) infection. Confocal microscopy revealed that PsV transport to the trans-Golgi network (TGN) was significantly reduced in Rab14 KO cells. Reintroduction of wild-type Rab14 restored infection levels, but neither GDP-bound (S25N) nor GTP-bound (Q70L) mutants did. S25N preferentially localized to the TGN, while Q70L exhibited similar localization in the early endosome and the TGN. PsV showed reduced colocalization with S25N, whereas the opposite was observed for Q70L. These results indicate that Rab14 GTPase cycling controls HPV transport to the TGN.

Rab14调节人乳头瘤病毒的运输到反式高尔基网络的感染性细胞进入。
人乳头瘤病毒(HPV)利用多种宿主蛋白感染上皮细胞。在这里,我们发现Rab14,一个属于rabb家族的小GTPase,是HPV感染的关键宿主因子。Rab14敲除(KO)细胞表现出对HPV假病毒粒子(PsV)感染的抗性。共聚焦显微镜显示,在Rab14 KO细胞中,PsV向反式高尔基网络(TGN)的转运显著减少。重新引入野生型Rab14恢复了感染水平,但gtp结合(S25N)和gtp结合(Q70L)突变体都没有恢复感染水平。S25N优先定位于TGN,而Q70L在早期核内体和TGN中表现出相似的定位。PsV与S25N的共定位减少,而Q70L则相反。这些结果表明Rab14 GTPase循环控制HPV向TGN的转运。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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