Evidence map›Paper›PMID 30393075›Full record

ArticleDevelopmental cell2018

A Robust Transposon-Endogenizing Response from Germline Stem Cells.

Sungjin Moon, Madeline Cassani, Yu An Lin, Lu Wang, Kun Dou, Zz Zhao Zhang

Abstract read
In one paragraph

Article in Developmental cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
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  9. PeerJ · 2025
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  12. Review
  13. Experimentally evolvingGenome research · 2024
    Article
  14. Genomes of historical specimens reveal multiple invasions of LTR retrotransposons inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Article
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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 2 institutions in 1 country.

Sungjin MoonDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.
Madeline CassaniDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.
Yu An LinDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.
Lu WangDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.
Kun DouDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.
Zz Zhao ZhangDepartment of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA. Electronic address: zzhang@carnegiescience.edu.
Department of Embryology · USCarnegie Institution for Science · US

Funding

Somatic transposition-mediated genome variegation during development, disease and aging conditionsDP5OD021355 · OD · DUKE UNIVERSITY · PI ZHANG, ZHAO · 2015 to 2019
$2.0M
NIH HHS DP5 OD021355
6 · The paper itself

Abstract

The heavy occupancy of transposons in the genome implies that existing organisms have survived from multiple, independent rounds of transposon invasions. However, how and which host cell types survive the initial wave of transposon invasion remain unclear. We show that the germline stem cells can initiate a robust adaptive response that rapidly endogenizes invading P element transposons by activating the DNA damage checkpoint and piRNA production. We find that temperature modulates the P element activity in germline stem cells, establishing a powerful tool to trigger transposon hyper-activation. Facing vigorous invasion, Drosophila first shut down oogenesis and induce selective apoptosis. Interestingly, a robust adaptive response occurs in ovarian stem cells through activation of the DNA damage checkpoint. Within 4 days, the hosts amplify P element-silencing piRNAs, repair DNA damage, subdue the transposon, and reinitiate oogenesis. We propose that this robust adaptive response can bestow upon organisms the ability to survive recurrent transposon invasions throughout evolution.

Indexed as

DNA Transposable ElementsGene SilencingHeat-Shock ResponseAnimalsCheckpoint Kinase 2DNA DamageDrosophila melanogasterDrosophila ProteinsFemaleOvumRNA, Small InterferingCheckpoint Kinase 2DNA Transposable ElementsDrosophila Proteinslok protein, DrosophilaRNA, Small Interfering

Identifiers

PMID30393075
PMCPMC6631374
OpenAlexW2899363025

What OpenQuestion holds

Textmetadata
LicenceTDM
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.