Evidence map›Paper›PMID 26240377›Full record

ArticleNucleic acids research2015

Telomeric repeat silencing in germ cells is essential for early development in Drosophila.

Valeriya Morgunova, Natalia Akulenko, Elizaveta Radion, Ivan Olovnikov, Yuri Abramov, Ludmila V Olenina, Sergey Shpiz, Daria V Kopytova, Sofia G Georgieva, Alla Kalmykova

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Telomere Checkpoint in Development and Aging.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Heterochromatin as an Important Driver of Genome Organization.Frontiers in cell and developmental biology · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Valeriya MorgunovaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Natalia AkulenkoInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Elizaveta RadionInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Ivan OlovnikovInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Yuri AbramovInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Ludmila V OleninaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Sergey ShpizInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Daria V KopytovaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Sofia G GeorgievaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation.
Alla KalmykovaInstitute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russian Federation allakalm@img.ras.ru.
Institute of Molecular Genetics · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The germline-specific role of telomeres consists of chromosome end elongation and proper chromosome segregation during early developmental stages. Despite the crucial role of telomeres in germ cells, little is known about telomere biology in the germline. We analyzed telomere homeostasis in the Drosophila female germline and early embryos. A novel germline-specific function of deadenylase complex Ccr4-Not in the telomeric transcript surveillance mechanism is reported. Depletion of Ccr4-Not complex components causes strong derepression of the telomeric retroelement HeT-A in the germ cells, accompanied by elongation of the HeT-A poly(A) tail. Dysfunction of transcription factors Woc and Trf2, as well as RNA-binding protein Ars2, also results in the accumulation of excessively polyadenylated HeT-A transcripts in ovaries. Germline knockdowns of Ccr4-Not components, Woc, Trf2 and Ars2, lead to abnormal mitosis in early embryos, characterized by chromosome missegregation, centrosome dysfunction and spindle multipolarity. Moreover, the observed phenotype is accompanied by the accumulation of HeT-A transcripts around the centrosomes in early embryos, suggesting the putative relationship between overexpression of telomeric transcripts and mitotic defects. Our data demonstrate that Ccr4-Not, Woc, Trf2 and Ars2, components of different regulatory pathways, are required for telomere protection in the germline in order to guarantee normal development.

Indexed as

Gene Expression Regulation, DevelopmentalGene SilencingRetroelementsTelomereAnimalsCarrier ProteinsDNA-Binding ProteinsDrosophilaDrosophila ProteinsEmbryonic DevelopmentFemaleMitosisOvaryOvumPolyadenylationRibonucleasesCarrier ProteinsCCR4 protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsNOT1 protein, DrosophilaRetroelementsRibonucleasesRNA-Binding ProteinsTelomeric Repeat Binding Protein 2Transcription FactorsTRF2 protein, DrosophilaWOC protein, Drosophila

Identifiers

PMID26240377
PMCPMC4605298
OpenAlexW1840847702

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.