PLoS PathogensMicrobiologyPeer-reviewed journal article
SV40 exploits the Nesprin-2-SUN1-KPNA4 axis for stepwise targeting and entry into the host nucleus to promote infection
Abstract
Many DNA viruses including polyomaviruses (PyVs) enter the host nucleus to cause infection, although how this is accomplished is unclear. To infect cells, the prototype PyV SV40 targets to the Nesprin-2 outer nuclear membrane protein and enters the nucleus via the nuclear pore complex (NPC). Host factors that function with Nesprin-2 to target SV40 to the nuclear membrane and drive NPC-dependent nuclear entry are unknown. Here we demonstrate that the SUN1 inner nuclear membrane protein acts coordinately with its binding-partner Nesprin-2 to target cytosol-localized SV40 to the nuclear membrane. Strikingly, despite localizing to the perinuclear space, the SUN domain of SUN1 plays a crucial role in Nesprin-2-dependent recruitment of cytosolic SV40. After targeting, SV40 binds to the NPC-associated importin receptor KPNA4, which translocates the virus into the nucleus. Our results reveal how a DNA virus exploits the Nesprin-2-SUN1-KPNA4 axis for stepwise targeting and entry into the nucleus to cause infection. Author summaryNuclear entry is required for most DNA viruses to cause infection, although the molecular mechanism of this step remains enigmatic. The DNA virus SV40 targets to the nuclear membrane by exploiting the Nesprin-2 outer nuclear membrane protein. In this study, we report that the SUN1 inner nuclear membrane protein functions with Nesprin-2 to target SV40 to the nuclear membrane, followed by nuclear entry of the virus via the action of the KNPA4 importin receptor.
- organism: human
- research focus: host-pathogen & immune response
- research focus: cell signaling & trafficking
- research focus: cell type annotation
- approach: experimental assay
- approach: wet-lab / biochemical assay
- Citations
- 0
- FWCI
- 0.00
- Field percentile
- 39th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- SV40 polyomavirus activates the Ras-MAPK signaling pathway for vacuolization, cell death, and virus release
N. Motamedi, X. Sewald, … D. DiMaio·bioRxiv·Oct 28, 2018
- The Herpes Simplex Virus pUL16 and pUL21 Proteins Prevent Capsids from Docking at Nuclear Pore Complexes
E. C. M. Thomas, R. L. Finnen, … B. W. Banfield·bioRxiv·Jun 21, 2023
- A requirement for Potassium and Calcium Channels during the Endosomal Trafficking of Polyomavirus Virions
S. J. Dobson, J. Mankouri, A. Whitehouse·bioRxiv·Oct 22, 2019
- Golgi-associated nuclear import receptor importin-7 targets HPV from the Golgi to the nucleus to promote infection
Tai-Ting Woo, Yuka Takeo, … Billy Tsai·Science AdvancesPeer-reviewed·Oct 22, 2025
- Inhibition of HIV infection by structural proteins of the inner nuclear membrane is associated with reduced chromatin dynamics
A. Bhargava, M. Maurin, … N. Manel·bioRxiv·Dec 3, 2020
- The nuclear localization signal of CPSF6 governs post-nuclear import steps of HIV-1 infection
Nicholas Rohlfes, Rajalingam Radhakrishnan, … Edward M. Campbell·PLoS PathogensPeer-reviewed·Jan 17, 2025