Evidence map›Paper›PMID 38348929›Full record

ArticleNucleic acids research2024

Human CST complex restricts excessive PrimPol repriming upon UV induced replication stress by suppressing p21.

Pau Biak Sang, Rishi K Jaiswal, Xinxing Lyu, Weihang Chai

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 33% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Pau Biak SangDepartment of Cancer Biology, Cardinal Bernardin Cancer Center, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.ORCID 0000-0001-7261-5117
Rishi K JaiswalDepartment of Cancer Biology, Cardinal Bernardin Cancer Center, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
Xinxing LyuDepartment of Cancer Biology, Cardinal Bernardin Cancer Center, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
Weihang ChaiDepartment of Cancer Biology, Cardinal Bernardin Cancer Center, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.ORCID 0000-0003-1206-2324
Rosalind Franklin University of Medicine and Science · USLoyola University Chicago · USUniversity of Delhi · IN

Funding

Molecular Modulator of RPA and RAD51 in Maintaining Genome StabilityR01CA234266 · NCI · WASHINGTON STATE UNIVERSITY · PI Weihang Chai · 2019 to 2026
$2.4M
Molecular Basis of Coats Plus DiseaseR01GM146376 · NIGMS · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI Weihang Chai · 2023 to 2026
$1.7M
Identification of a novel tumor suppressorof melanoma and UV-induced genome instabilityR21ES034636 · NIEHS · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI CHAI, WEIHANG · 2022 to 2023
$429k
NCI NIH HHS R01 CA234266NIEHS NIH HHS R21 ES034636NIGMS NIH HHS R01 GM146376NIH HHS R01GM146376
6 · The paper itself

Abstract

DNA replication stress, caused by various endogenous and exogenous agents, halt or stall DNA replication progression. Cells have developed diverse mechanisms to tolerate and overcome replication stress, enabling them to continue replication. One effective strategy to overcome stalled replication involves skipping the DNA lesion using a specialized polymerase known as PrimPol, which reinitiates DNA synthesis downstream of the damage. However, the mechanism regulating PrimPol repriming is largely unclear. In this study, we observe that knockdown of STN1 or CTC1, components of the CTC1/STN1/TEN1 complex, leads to enhanced replication progression following UV exposure. We find that such increased replication is dependent on PrimPol, and PrimPol recruitment to stalled forks increases upon CST depletion. Moreover, we find that p21 is upregulated in STN1-depleted cells in a p53-independent manner, and p21 depletion restores normal replication rates caused by STN1 deficiency. We identify that p21 interacts with PrimPol, and STN1 depletion stimulates p21-PrimPol interaction and facilitates PrimPol recruitment to stalled forks. Our findings reveal a previously undescribed interplay between CST, PrimPol and p21 in promoting repriming in response to stalled replication, and shed light on the regulation of PrimPol repriming at stalled forks.

Indexed as

Cyclin-Dependent Kinase Inhibitor p21DNA-Directed DNA PolymeraseDNA PrimaseDNA ReplicationMultifunctional EnzymesTelomere-Binding ProteinsUltraviolet RaysDNA DamageHumansTumor Suppressor Protein p53CDKN1A protein, humanCtc1 protein, humanCyclin-Dependent Kinase Inhibitor p21DNA-Directed DNA PolymeraseDNA PrimaseMultifunctional EnzymesPrimPol protein, humanStn1 protein, humanTelomere-Binding ProteinsTen1 protein, humanTumor Suppressor Protein p53

Identifiers

PMID38348929
PMCPMC11040158
OpenAlexW4391780161

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.