Evidence map›Paper›PMID 31391501›Full record

ArticleScientific reports2019

Role of p53 isoforms in the DNA damage response during Drosophila oogenesis.

Ji-Hong Park, Tram Thi Ngoc Nguyen, Eun-Mi Lee, Veronica Castro-Aceituno, Ram Wagle, Kwang-Soon Lee, Juyoung Choi, Young-Han Song

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. 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
1.1field-weighted citation impact, top 20% 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, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Role of p53 in Regulating Radiation Responses.Life (Basel, Switzerland) · 2022
    Review
  5. eLife · 2022
    Article
  6. Regulation and coordination of the different DNA damage responses inFrontiers in cell and developmental biology · 2022
    Review
  7. Article
  8. Review
  9. Article
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

8 authors at 1 institution in 1 country.

Ji-Hong ParkDepartment of Biomedical Gerontology, Hallym University, Chuncheon, Gangwon-do, Republic of Korea.
Tram Thi Ngoc NguyenDepartment of Biomedical Gerontology, Hallym University, Chuncheon, Gangwon-do, Republic of Korea.
Eun-Mi LeeIlsong Institute of Life Science, Hallym University, Anyang, Gyeonggi-do, Republic of Korea.ORCID http://orcid.org/0000-0002-1995-2867
Veronica Castro-AceitunoIlsong Institute of Life Science, Hallym University, Anyang, Gyeonggi-do, Republic of Korea.ORCID http://orcid.org/0000-0002-5285-3975
Ram WagleDepartment of Biomedical Gerontology, Hallym University, Chuncheon, Gangwon-do, Republic of Korea.
Kwang-Soon LeeIlsong Institute of Life Science, Hallym University, Anyang, Gyeonggi-do, Republic of Korea.
Juyoung ChoiIlsong Institute of Life Science, Hallym University, Anyang, Gyeonggi-do, Republic of Korea.
Young-Han SongDepartment of Biomedical Gerontology, Hallym University, Chuncheon, Gangwon-do, Republic of Korea. ysong@hallym.ac.kr.ORCID http://orcid.org/0000-0002-0758-3654
Hallym University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor suppressor p53 is involved in the DNA damage response and induces cell cycle arrest or apoptosis upon DNA damage. Drosophila p53 encodes two isoforms, p53A and p53B, that induce apoptosis in somatic cells. To investigate the roles of Drosophila p53 isoforms in female germline cells, the DNA damage response was analyzed in the adult ovary. Early oogenesis was sensitive to irradiation and lok-, p53-, and hid-dependent cell death occurred rapidly after both low- and high-dose irradiation. Both p53 isoforms were responsible for this cell death. On the other hand, delayed cell death in mid-oogenesis was induced at a low level only after high-dose irradiation in a p53-independent manner. The daily egg production, which did not change after low-dose irradiation, was severely reduced after high-dose irradiation in p53 mutant females due to the loss of germline stem cells. When the p53A or p53B isoform was expressed in the germline cells in the p53 mutant females at levels that do not affect normal oogenesis, p53A, but not p53B, restored the fertility of the irradiated female. In summary, moderate expression of p53A is critical to maintain the function of germline stem cells during normal oogenesis as well as after high-dose irradiation.

Indexed as

DNA RepairAnimalsAnimals, Genetically ModifiedApoptosisDNA DamageDrosophilaDrosophila ProteinsFemaleFertilityMaleMutationOogenesisOvumProtein IsoformsSpermatozoaTumor Suppressor Protein p53Drosophila Proteinsp53 protein, DrosophilaProtein IsoformsTumor Suppressor Protein p53

Identifiers

PMID31391501
PMCPMC6685966
OpenAlexW2966242666

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.