Evidence map›Paper›PMID 37609143›Full record

ArticlebioRxiv : the preprint server for biology2023

Non-homologous end joining shapes the genomic rearrangement landscape of chromothripsis from mitotic errors.

Qing Hu, Jose Espejo Valle-Inclan, Rashmi Dahiya, Alison Guyer, Alice Mazzagatti, Elizabeth G Maurais, Justin L Engel, Isidro Cortés-Ciriano, Peter Ly

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Qing HuDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Jose Espejo Valle-InclanEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Rashmi DahiyaDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Alison GuyerDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Alice MazzagattiDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Elizabeth G MauraisDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Justin L EngelDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
Isidro Cortés-CirianoEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Peter LyDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, United States.
The University of Texas Southwestern Medical Center · USEuropean Bioinformatics Institute · GBUniversity of Pittsburgh · US

Funding

Genomic Instability from Fragmented Chromosomes in MicronucleiR35GM146610 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Peter Ly · 2022 to 2026
$2.3M
NIGMS NIH HHS R35 GM146610
6 · The paper itself

Abstract

Errors in mitosis can generate micronuclei that entrap mis-segregated chromosomes, which are susceptible to catastrophic fragmentation through a process termed chromothripsis. The reassembly of fragmented chromosomes by error-prone DNA double-strand break (DSB) repair generates a spectrum of simple and complex genomic rearrangements that are associated with human cancers and disorders. How specific DSB repair pathways recognize and process these lesions remains poorly understood. Here we used CRISPR/Cas9 to systematically inactivate distinct DSB processing or repair pathways and interrogated the rearrangement landscape of fragmented chromosomes from micronuclei. Deletion of canonical non-homologous end joining (NHEJ) components, including DNA-PKcs, LIG4, and XLF, substantially reduced the formation of complex rearrangements and shifted the rearrangement landscape toward simple alterations without the characteristic patterns of cancer-associated chromothripsis. Following reincorporation into the nucleus, fragmented chromosomes localize within micronuclei bodies (MN bodies) and undergo successful ligation by NHEJ within a single cell cycle. In the absence of NHEJ, chromosome fragments were rarely engaged by polymerase theta-mediated alternative end-joining or recombination-based mechanisms, resulting in delayed repair kinetics and persistent 53BP1-labeled MN bodies in the interphase nucleus. Prolonged DNA damage signaling from unrepaired fragments ultimately triggered cell cycle arrest. Thus, we provide evidence supporting NHEJ as the exclusive DSB repair pathway generating complex rearrangements following chromothripsis from mitotic errors.

Identifiers

PMID37609143
PMCPMC10441393
OpenAlexW4385780919

What OpenQuestion 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 OpenQuestion graph.