Evidence map›Paper›PMID 24036543›Full record

ArticleCell cycle (Georgetown, Tex.)2013

Laser microbeam-induced DNA damage inhibits cell division in fertilized eggs and early embryos.

Zhong-Wei Wang, Xue-Shan Ma, Jun-Yu Ma, Yi-Bo Luo, Fei Lin, Zhen-Bo Wang, Heng-Yu Fan, Heide Schatten, Qing-Yuan Sun

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Cleavage of Early Mouse Embryo with Damaged DNA.International journal of molecular sciences · 2022
    Article
  4. Article
  5. DNA damage repair is suppressed in porcine aged oocytes.Journal of animal science and technology · 2021
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Zhong-Wei WangState Key Laboratory of Reproductive Biology; Institute of Zoology; Chinese Academy of Sciences; Beijing, China.
Xue-Shan Ma
Jun-Yu Ma
Yi-Bo Luo
Fei Lin
Zhen-Bo Wang
Heng-Yu Fan
Heide Schatten
Qing-Yuan Sun
Chinese Academy of Sciences · CNInstitute of Zoology · CNMissouri College · USZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA double-strand breaks are caused by both intracellular physiological processes and environmental stress. In this study, we used laser microbeam cut (abbreviated microcut or cut), which allows specific DNA damage in the pronucleus of a fertilized egg and in individual blastomere(s) of an early embryo, to investigate the response of early embryos to DNA double-strand breaks. Line type γH2AX foci were detected in the cut region, while Chk2 phosphorylation staining was observed in the whole nuclear region of the cut pronuclei or blastomeres. Zygotes with cut male or female pronucleus showed poor developmental capability: the percentage of cleavage embryos was significantly decreased, and the embryos failed to complete further development to blastocysts. The cut blastomeres in 2-cell, 4-cell, and 8-cell embryos ceased cleavage, and they failed to incorporate into compacted morulae, but instead underwent apoptosis and cell death at the blastocyst stage; the uncut part of embryos could develop to blastocysts, with a reduced percentage or decreased cell number. When both blastomeres of the 2-cell embryos were cut by laser microbeam, cell death occurred 24 h earlier, suggesting important functions of the uncut blastomere in delaying cell death of the cut blastomere. Taken together, we conclude that microbeam-induced DNA damage in early embryos causes compromised development, and that embryos may have their own mechanisms to exclude DNA-damaged blastomeres from participating in further development.

Indexed as

Cell DivisionDNA DamageLasersAnimalsBlastomeresCDX2 Transcription FactorCell LineageEmbryo, MammalianEmbryonic DevelopmentFemaleFertilizationHomeodomain ProteinsMaleMice, Inbred ICRMorulaOctamer Transcription Factor-3Cdx2 protein, mouseCDX2 Transcription FactorHomeodomain ProteinsOctamer Transcription Factor-3Pou5f1 protein, mouseTranscription FactorsblastomeresDNA damageembryoslaser micro beamzygotes

Identifiers

PMID24036543
PMCPMC3885644
OpenAlexW2081418215

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.