Evidence map›Paper›PMID 39829879›Full record

ArticlebioRxiv : the preprint server for biology2025

Complex roles for proliferating cell nuclear antigen in restricting human cytomegalovirus replication.

Pierce Longmire, Olivia Daigle, Sebastian Zeltzer, Matias Lee, Marek Svoboda, Marco Padilla-Rodriguez, Carly Bobak, Giovanni Bosco, Felicia Goodrum

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Pierce LongmireGraduate Program in Molecular Medicine, University of Arizona, Tucson, Arizona, USA.ORCID 0000-0001-8875-6053
Olivia DaigleDepartment of Molecular and Systems Biology, Dartmouth Geisel College of Medicine, Hanover, New Hampshire, USA.
Sebastian ZeltzerBIO5 Institute, University of Arizona, Tucson, Arizona, USA.
Matias LeeResearch Computing and Data Services, Information, Technology, and Consulting, Dartmouth College, Hanover, New Hampshire, USA.
Marek SvobodaDepartment of Molecular and Systems Biology, Dartmouth Geisel College of Medicine, Hanover, New Hampshire, USA.ORCID 0000-0002-5166-673X
Marco Padilla-RodriguezMicroscopy Shared Resource, University of Arizona Cancer Center, Tucson, Arizona, USA.
Carly BobakResearch Computing and Data Services, Information, Technology, and Consulting, Dartmouth College, Hanover, New Hampshire, USA.
Giovanni BoscoDepartment of Molecular and Systems Biology, Dartmouth Geisel College of Medicine, Hanover, New Hampshire, USA.
Felicia GoodrumGraduate Program in Molecular Medicine, University of Arizona, Tucson, Arizona, USA.ORCID 0000-0002-6646-7290

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
Mechanisms of Human Cytomegalovirus Latency in Primary Human Hematopoietic CellsR01AI079059 · NIAID · UNIVERSITY OF ARIZONA · PI GOODRUM, FELICIA D · 2008 to 2018
$4.4M
Mechanisms of Human Cytomegalovirus Latency in Primary Human Hematopoietic CellsR37AI079059 · NIAID · UNIVERSITY OF ARIZONA · PI Felicia D Goodrum · 2019 to 2026
$3.3M
Host DNA repair pathways in human cytomegalovirus replicationR01AI177392 · NIAID · UNIVERSITY OF ARIZONA · PI Giovanni Bosco, Felicia D Goodrum · 2023 to 2026
$3.0M
Structured Illumination Fluorescence MicroscopeS10OD019948 · OD · UNIVERSITY OF ARIZONA · PI ELLIOTT, DAVID A · 2015 to 2015
$517k
NCI NIH HHS P30 CA023074NIAID NIH HHS R01 AI079059NIAID NIH HHS R01 AI177392NIAID NIH HHS R37 AI079059NIH HHS S10 OD019948
6 · The paper itself

Abstract

DNA viruses at once elicit and commandeer host pathways, including DNA repair pathways for virus replication. Despite encoding its own DNA polymerase and processivity factor, human cytomegalovirus (HCMV) recruits the cellular processivity factor, proliferating cell nuclear antigen (PCNA) and specialized host DNA polymerases involved in translesion synthesis (TLS) to replication compartments (RCs) where viral DNA (vDNA) is synthesized. While the recruitment of TLS polymerases is important for viral genome stability, the role of PCNA is poorly understood. PCNA function in DNA repair is regulated by monoubiquitination (mUb) or SUMOylation of PCNA at lysine 164 (K164). We find that mUb-PCNA increases over the course of infection, and modification of K164 is required for PCNA-mediated restriction of virus replication. mUb-PCNA plays important known roles in recruiting TLS polymerases to DNA, which we have shown are important for viral genome integrity and diversity, represented by novel junctions and single nucleotide variants (SNVs), respectively. We find that PCNA drives SNVs on vDNA similar to Y-family TLS polymerases, but that this did not require modification at K164. Unlike TLS polymerases, PCNA was dispensable for preventing large scale rearrangements on vDNA. These striking results suggest separable PCNA-dependent and - independent functions of TLS polymerases on vDNA. By extension, these results imply roles for TLS polymerase beyond their canonical function in TLS in host biology. These findings highlight PCNA as a complex restriction factor for HCMV infection, likely with multiple distinct roles, and provides new insights into the PCNA-mediated regulation of DNA synthesis and repair in viral infection.

Identifiers

PMID39829879
PMCPMC11741387

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.