Evidence map›Paper›PMID 33836577›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

A conserved Ctp1/CtIP C-terminal peptide stimulates Mre11 endonuclease activity.

Aleksandar Zdravković, James M Daley, Arijit Dutta, Tatsuya Niwa, Yasuto Murayama, Shuji Kanamaru, Kentaro Ito, Takahisa Maki, Bilge Argunhan, Masayuki Takahashi and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Key molecular DNA damage responses of human cells to radiation.Frontiers in cell and developmental biology · 2024
    Review
  8. Dynamic Properties of the DNA Damage Response Mre11/Rad50 Complex.International journal of molecular sciences · 2023
    Review
  9. Article
  10. DNA end resection during homologous recombination.Current opinion in genetics & development · 2021
    Review
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

13 authors at 3 institutions in 2 countries.

Aleksandar ZdravkovićSchool and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Kanagawa 226-8503, Japan.ORCID 0000-0002-9494-9350
James M DaleyDepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX 78229.
Arijit DuttaDepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX 78229.ORCID 0000-0002-5675-0092
Tatsuya NiwaSchool and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Kanagawa 226-8503, Japan.ORCID 0000-0002-1330-8974
Yasuto MurayamaCenter for Frontier Research, National Institute of Genetics, Shizuoka 411-8540, Japan.ORCID 0000-0002-6866-0748
Shuji KanamaruSchool and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Kanagawa 226-8503, Japan.ORCID 0000-0002-2765-531X
Kentaro ItoInstitute of Innovative Research, Tokyo Institute of Technology, Kanagawa 226-8503, Japan.ORCID 0000-0001-9221-5188
Takahisa MakiInstitute of Innovative Research, Tokyo Institute of Technology, Kanagawa 226-8503, Japan.
Bilge ArgunhanInstitute of Innovative Research, Tokyo Institute of Technology, Kanagawa 226-8503, Japan.ORCID 0000-0002-6023-7654
Masayuki TakahashiSchool and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Kanagawa 226-8503, Japan.ORCID 0000-0002-1856-5312
Hideo TsubouchiSchool and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Kanagawa 226-8503, Japan; htsubouchi@bio.titech.ac.jp sungp@uthscsa.edu hiwasaki@bio.titech.ac.jp.ORCID 0000-0003-0814-8432
Patrick SungDepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX 78229; htsubouchi@bio.titech.ac.jp sungp@uthscsa.edu hiwasaki@bio.titech.ac.jp.
Hiroshi IwasakiSchool and Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Kanagawa 226-8503, Japan; htsubouchi@bio.titech.ac.jp sungp@uthscsa.edu hiwasaki@bio.titech.ac.jp.ORCID 0000-0002-0153-6873
Tokyo Institute of Technology · JPThe University of Texas Health Science Center at San Antonio · USNational Institute of Genetics · JP

Funding

Mechanisms of DNA Homology-directed Genome Repair and Tumor SuppressionR35CA241801 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SUNG, PATRICK · 2019 to 2025
$6.0M
NCI NIH HHS R35 CA241801
6 · The paper itself

Abstract

The Mre11-Rad50-Nbs1 complex (MRN) is important for repairing DNA double-strand breaks (DSBs) by homologous recombination (HR). The endonuclease activity of MRN is critical for resecting 5'-ended DNA strands at DSB ends, producing 3'-ended single-strand DNA, a prerequisite for HR. This endonuclease activity is stimulated by Ctp1, the

Indexed as

Amino Acid SequenceCasein Kinase IIConserved SequenceDNA-Binding ProteinsDNA Breaks, Double-StrandedExodeoxyribonucleasesPeptidesPhosphorylationSchizosaccharomycesSchizosaccharomyces pombe ProteinsCasein Kinase IICtp1 protein, S pombeDNA-Binding ProteinsExodeoxyribonucleasesMre11 protein, S pombePeptidesSchizosaccharomyces pombe ProteinsCtp1/CtIPdouble-strand break repairfission yeasthomologous recombinationMre11-Rad50-Nbs1

Identifiers

PMID33836577
PMCPMC7980430
OpenAlexW3135075556

What OpenQuestion holds

Textmetadata
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.