Evidence map›Paper›PMID 36552858›Full record

ArticleCells2022

TRIP13 Participates in Immediate-Early Sensing of DNA Strand Breaks and ATM Signaling Amplification through MRE11.

Hyeongsun Jeong, Minwoo Wie, In-Joon Baek, Gyuwon Sohn, Si-Hyeon Um, Seon-Gyeong Lee, Yuri Seo, Jaesun Ra, Eun A Lee, Shinseog Kim and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

16 authors at 3 institutions in 2 countries.

Hyeongsun JeongCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Minwoo WieCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
In-Joon BaekCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Gyuwon SohnCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Si-Hyeon UmCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Seon-Gyeong LeeCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Yuri SeoCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Jaesun RaCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.ORCID 0000-0001-9588-3544
Eun A LeeCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Shinseog KimCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Byung Gyu KimCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Rajashree A DeshpandeDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA.
Tanya T PaullDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA.
Joo Seok HanCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Taejoon KwonCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.ORCID 0000-0002-9794-6112
Kyungjae MyungCenter for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.ORCID 0000-0001-7975-6190
Institute for Basic Science · KRThe University of Texas at Austin · USChungnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thyroid hormone receptor-interacting protein 13 (TRIP13) participates in various regulatory steps related to the cell cycle, such as the mitotic spindle assembly checkpoint and meiotic recombination, possibly by interacting with members of the HORMA domain protein family. Recently, it was reported that TRIP13 could regulate the choice of the DNA repair pathway, i.e., homologous recombination (HR) or nonhomologous end-joining (NHEJ). However, TRIP13 is recruited to DNA damage sites within a few seconds after damage and may therefore have another function in DNA repair other than regulation of the pathway choice. Furthermore, the depletion of TRIP13 inhibited both HR and NHEJ, suggesting that TRIP13 plays other roles besides regulation of choice between HR and NHEJ. To explore the unidentified functions of TRIP13 in the DNA damage response, we investigated its genome-wide interaction partners in the context of DNA damage using quantitative proteomics with proximity labeling. We identified MRE11 as a novel interacting partner of TRIP13. TRIP13 controlled the recruitment of MDC1 to DNA damage sites by regulating the interaction between MDC1 and the MRN complex. Consistently, TRIP13 was involved in ATM signaling amplification. Our study provides new insight into the function of TRIP13 in immediate-early DNA damage sensing and ATM signaling activation.

Indexed as

DNA-Binding ProteinsNuclear ProteinsDNADNA Breaks, Double-StrandedDNA DamageMRE11 Homologue ProteinDNADNA-Binding ProteinsMRE11 Homologue ProteinNuclear ProteinsDNA damage responseHORMA domainMRN complexTRIP13

Identifiers

PMID36552858
PMCPMC9776959
OpenAlexW4312195493

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.