Evidence map›Paper›PMID 26286192›Full record

ArticleNucleic acids research2015

Involvement of SRSF11 in cell cycle-specific recruitment of telomerase to telomeres at nuclear speckles.

Ji Hoon Lee, Sun Ah Jeong, Prabhat Khadka, Juyeong Hong, In Kwon Chung

Open 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. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. ScRNA-seq Data Reveal Gene Upregulation and Downregulation in Oxygen-Induced Retinopathy.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Article
  3. NNature cell biology · 2026
    Article
  4. Review
  5. Observational
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Telomeres and Cancer.Life (Basel, Switzerland) · 2021
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Tying up loose ends: telomeres, genomic instability and lamins.Current opinion in genetics & development · 2016
    Review
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

5 authors at 1 institution in 1 country.

Ji Hoon LeeDepartments of Systems Biology and Integrated Omics for Biomedical Science, Yonsei University, Seoul 120-749, Korea.
Sun Ah JeongDepartments of Systems Biology and Integrated Omics for Biomedical Science, Yonsei University, Seoul 120-749, Korea.
Prabhat KhadkaDepartments of Systems Biology and Integrated Omics for Biomedical Science, Yonsei University, Seoul 120-749, Korea.
Juyeong HongDepartments of Systems Biology and Integrated Omics for Biomedical Science, Yonsei University, Seoul 120-749, Korea.
In Kwon ChungDepartments of Systems Biology and Integrated Omics for Biomedical Science, Yonsei University, Seoul 120-749, Korea topoviro@yonsei.ac.kr.
Yonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Telomerase, a unique ribonucleoprotein complex that contains the telomerase reverse transcriptase (TERT), the telomerase RNA component (TERC) and the TERC-binding protein dyskerin, is required for continued cell proliferation in stem cells and cancer cells. Here we identify SRSF11 as a novel TERC-binding protein that localizes to nuclear speckles, subnuclear structures that are enriched in pre-messenger RNA splicing factors. SRSF11 associates with active telomerase enzyme through an interaction with TERC and directs it to nuclear speckles specifically during S phase of the cell cycle. On the other hand, a subset of telomeres is shown to be constitutively present at nuclear speckles irrespective of cell cycle phase, suggesting that nuclear speckles could be the nuclear sites for telomerase recruitment to telomeres. SRSF11 also associates with telomeres through an interaction with TRF2, which facilitates translocation of telomerase to telomeres. Depletion of SRSF11 prevents telomerase from associating with nuclear speckles and disrupts telomerase recruitment to telomeres, thereby abrogating telomere elongation by telomerase. These findings suggest that SRSF11 acts as a nuclear speckle-targeting factor that is essential for telomerase association with telomeres through the interactions with TERC and TRF2, and provides a potential target for modulating telomerase activity in cancer.

Indexed as

Cell CycleCell Line, TumorCell Nucleus StructuresHeLa CellsHumansProtein Interaction Domains and MotifsRNASerine-Arginine Splicing FactorsTelomeraseTelomereTelomere HomeostasisTelomeric Repeat Binding Protein 2RNASerine-Arginine Splicing FactorsSRSF11 protein, humanTelomerasetelomerase RNATelomeric Repeat Binding Protein 2

Identifiers

PMID26286192
PMCPMC4787792
OpenAlexW2131835933

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.