Evidence map›Paper›PMID 26000719›Full record

ArticleAging2015

Requirement of ATR for maintenance of intestinal stem cells in aging Drosophila.

Joung-Sun Park, Hyun-Jin Na, Jung-Hoon Pyo, Ho-Jun Jeon, Young-Shin Kim, Mi-Ae Yoo

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. International journal of molecular sciences · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Biomarkers of aging.Science China. Life sciences · 2023
    Review
  6. Review
  7. Oncology letters · 2018
    Article
  8. Article
  9. 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

6 authors at 1 institution in 1 country.

Joung-Sun ParkDepartment of Molecular Biology, Pusan National University, Busan, 609-735, Republic of Korea.
Hyun-Jin NaDepartment of Molecular Biology, Pusan National University, Busan, 609-735, Republic of Korea.
Jung-Hoon PyoDepartment of Molecular Biology, Pusan National University, Busan, 609-735, Republic of Korea.
Ho-Jun JeonDepartment of Molecular Biology, Pusan National University, Busan, 609-735, Republic of Korea.
Young-Shin KimDepartment of Molecular Biology, Pusan National University, Busan, 609-735, Republic of Korea.
Mi-Ae YooDepartment of Molecular Biology, Pusan National University, Busan, 609-735, Republic of Korea.
Pusan National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The stem cell genomic stability forms the basis for robust tissue homeostasis, particularly in high-turnover tissues. For the genomic stability, DNA damage response (DDR) is essential. This study was focused on the role of two major DDR-related factors, ataxia telangiectasia-mutated (ATM) and ATM- and RAD3-related (ATR) kinases, in the maintenance of intestinal stem cells (ISCs) in the adultDrosophila midgut. We explored the role of ATM and ATR, utilizing immunostaining with an anti-pS/TQ antibody as an indicator of ATM/ATR activation, γ-irradiation as a DNA damage inducer, and the UAS/GAL4 system for cell type-specific knockdown of ATM, ATR, or both during adulthood. The results showed that the pS/TQ signals got stronger with age and after oxidative stress. The pS/TQ signals were found to be more dependent on ATR rather than on ATM in ISCs/enteroblasts (EBs). Furthermore, an ISC/EB-specific knockdown of ATR, ATM, or both decreased the number of ISCs and oxidative stress-induced ISC proliferation. The phenotypic changes that were caused by the ATR knockdown were more pronounced than those caused by the ATM knockdown; however, our data indicate that ATR and ATM are both needed for ISC maintenance and proliferation; ATR seems to play a bigger role than does ATM.

Indexed as

Adult Stem CellsAgingAnimalsAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsDrosophilaDrosophila ProteinsImmunohistochemistryIntestinesProtein Serine-Threonine KinasesStem CellsAtaxia Telangiectasia Mutated ProteinsCell Cycle ProteinsDrosophila ProteinsMei-41 protein, DrosophilaProtein Serine-Threonine KinasesTefu protein, DrosophilaagingATM/ATRDNA damage responseDrosophilaintestinal stem cell

Identifiers

PMID26000719
PMCPMC4468312
OpenAlexW2333191908

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.