Evidence map›Paper›PMID 34354233›Full record

ArticleNature cell biology2021

ASTE1 promotes shieldin-complex-mediated DNA repair by attenuating end resection.

Fei Zhao, Wootae Kim, Huanyao Gao, Chao Liu, Yong Zhang, Yuping Chen, Min Deng, Qin Zhou, Jinzhou Huang, Qi Hu and 14 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 46 citations in OpenAlex.

  1. Mechanisms and disease relevance of DNA break repair pathway choice.Nature reviews. Molecular cell biology · 2026
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  15. Syk-dependent homologous recombination activation promotes cancer resistance to DNA targeted therapy.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 6 institutions in 3 countries.

Fei Zhao *Department of Oncology, Mayo Clinic, Rochester, MN, USA.
Wootae Kim *Department of Oncology, Mayo Clinic, Rochester, MN, USA.
Huanyao GaoDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-9441-9579
Chao LiuDepartment of Cancer Genetics and Epigenetics, Beckman Research Institute of City of Hope, Duarte, CA, USA.
Yong ZhangDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Yuping ChenKey Laboratory of Arrhythmias of the Ministry of Education of China, Research Center for Translational Medicine, East Hospital, Tongji University School of Medicine, Shanghai, China.
Min DengDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0003-1987-9775
Qin ZhouDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Jinzhou HuangDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Qi HuDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0003-3647-8471
Shih-Hsun ChenInstitute of Biochemical Sciences, National Taiwan University, Taipei, Taiwan.
Somaira NowsheenDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-7174-5366
Jake A KloeberDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-6646-564X
Bo QinDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-8993-240X
Ping YinDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Xinyi TuDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Guijie GuoDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Sisi QinDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, MN, USA.
Chao ZhangDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Ming GaoDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Kuntian LuoDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.
Yilun LiuDepartment of Cancer Genetics and Epigenetics, Beckman Research Institute of City of Hope, Duarte, CA, USA.ORCID http://orcid.org/0000-0001-6884-8487
Zhenkun LouDepartment of Oncology, Mayo Clinic, Rochester, MN, USA. Lou.zhenkun@mayo.edu.ORCID http://orcid.org/0000-0003-1938-3091
Jian YuanKey Laboratory of Arrhythmias of the Ministry of Education of China, Research Center for Translational Medicine, East Hospital, Tongji University School of Medicine, Shanghai, China. yuanjian229@hotmail.com.ORCID http://orcid.org/0000-0002-2801-8849
Mayo Clinic in Arizona · USMayo Clinic · USCity of Hope · USTongji University · CNNational Taiwan University · TWUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The shieldin complex functions as the downstream effector of 53BP1-RIF1 to promote DNA double-strand break end-joining by restricting end resection. The SHLD2 subunit binds to single-stranded DNA ends and blocks end resection through OB-fold domains. Besides blocking end resection, it is unclear how the shieldin complex processes SHLD2-bound single-stranded DNA and promotes non-homologous end-joining. Here, we identify a downstream effector of the shieldin complex, ASTE1, as a structure-specific DNA endonuclease that specifically cleaves single-stranded DNA and 3' overhang DNA. ASTE1 localizes to DNA damage sites in a shieldin-dependent manner. Loss of ASTE1 impairs non-homologous end-joining, leads to hyper-resection and causes defective immunoglobulin class switch recombination. ASTE1 deficiency also causes resistance to poly(ADP-ribose) polymerase inhibitors in BRCA1-deficient cells owing to restoration of homologous recombination. These findings suggest that ASTE1-mediated 3' single-stranded DNA end cleavage contributes to the control of DSB repair choice by 53BP1, RIF1 and shieldin.

Indexed as

DNA End-Joining RepairAnimalsCell Cycle ProteinsDeoxyribonuclease IDNADNA-Binding ProteinsFemaleGenomic InstabilityHEK293 CellsHumansImmunoglobulin Class SwitchingMaleMiceMice, Inbred C57BLProteinsRecombinant Fusion ProteinsASTE1 protein, humanCell Cycle ProteinsDeoxyribonuclease IDNADNA-Binding ProteinsProteinsRecombinant Fusion ProteinsSHLD2 protein, human

Identifiers

PMID34354233
OpenAlexW3192619612

What OpenQuestion holds

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Registered trials

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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.