Evidence map›Paper›PMID 30262885›Full record

ArticleNature communications2018

Nuclear lamina dysfunction triggers a germline stem cell checkpoint.

Lacy J Barton, Tingting Duan, Wenfan Ke, Amy Luttinger, Kaylee E Lovander, Alexey A Soshnev, Pamela K Geyer

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

21 citing papers in PubMed, 28 citations in OpenAlex.

  1. International journal of molecular sciences · 2026
    Article
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  8. Nuclear actin is a critical regulator ofbioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
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  12. Article
  13. Article
  14. The phagocytic cyst cells inScience advances · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Survival ofDevelopment (Cambridge, England) · 2020
    Article
  19. Review
  20. 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

7 authors at 1 institution in 1 country.

Lacy J BartonDepartment of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA.ORCID http://orcid.org/0000-0001-9745-4946
Tingting DuanDepartment of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA.ORCID http://orcid.org/0000-0002-3671-6524
Wenfan KeDepartment of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA.ORCID http://orcid.org/0000-0002-7047-5445
Amy LuttingerDepartment of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA.
Kaylee E LovanderDepartment of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA.
Alexey A SoshnevDepartment of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA.ORCID http://orcid.org/0000-0002-1713-3470
Pamela K GeyerDepartment of Biochemistry, University of Iowa, Iowa City, IA, 52242, USA. pamela-geyer@uiowa.edu.ORCID http://orcid.org/0000-0001-9275-1407
University of Iowa · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
The Role of LEM Domain Proteins in Nuclear FunctionR01GM087341 · NIGMS · UNIVERSITY OF IOWA · PI GEYER, PAMELA K. · 2010 to 2022
$2.8M
Request for Funds to Purchase a Replacement Laser Scanning Confocal MicroscopeS10RR025439 · NCRR · UNIVERSITY OF IOWA · PI ZABNER, JOSEPH · 2009 to 2009
$500k
Damon Runyon Cancer Research Foundation (Damon Runyon) DRG-2185-14NCRR NIH HHS S10 RR025439NIGMS NIH HHS R01 GM087341U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) GM087341
6 · The paper itself

Abstract

LEM domain (LEM-D) proteins are conserved components of the nuclear lamina (NL) that contribute to stem cell maintenance through poorly understood mechanisms. The Drosophila emerin homolog Otefin (Ote) is required for maintenance of germline stem cells (GSCs) and gametogenesis. Here, we show that ote mutants carry germ cell-specific changes in nuclear architecture that are linked to GSC loss. Strikingly, we found that both GSC death and gametogenesis are rescued by inactivation of the DNA damage response (DDR) kinases, ATR and Chk2. Whereas the germline checkpoint draws from components of the DDR pathway, genetic and cytological features of the GSC checkpoint differ from the canonical pathway. Instead, structural deformation of the NL correlates with checkpoint activation. Despite remarkably normal oogenesis, rescued oocytes do not support embryogenesis. Taken together, these data suggest that NL dysfunction caused by Otefin loss triggers a GSC-specific checkpoint that contributes to maintenance of gamete quality.

Indexed as

Cell Cycle CheckpointsAnimalsCheckpoint Kinase 2DNA DamageDNA Transposable ElementsDrosophila melanogasterDrosophila ProteinsFemaleGerm CellsMaleMembrane ProteinsModels, BiologicalMutationNuclear LaminaNuclear ProteinsOogenesisCheckpoint Kinase 2DNA Transposable ElementsDrosophila ProteinsMembrane ProteinsNuclear ProteinsOte protein, Drosophila

Identifiers

PMID30262885
PMCPMC6160405
OpenAlexW2892256724

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.