Evidence map›Paper›PMID 24513678›Full record

ArticleNucleus (Austin, Tex.)

UBF complexes with phosphatidylinositol 4,5-bisphosphate in nucleolar organizer regions regardless of ongoing RNA polymerase I activity.

Margarita Sobol, Sukriye Yildirim, Vlada V Philimonenko, Pavel Marášek, Enrique Castaño, Pavel Hozák

Open access · goldAbstract read
In one paragraph

Article in Nucleus (Austin, Tex.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Small Nucleolar RNA fromNon-coding RNA · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. The nuclear phosphoinositide response to stress.Cell cycle (Georgetown, Tex.) · 2020
    Review
  19. Review
  20. 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

6 authors at 1 institution in 1 country.

Margarita SobolInstitute of Molecular Genetics ASCR v.v.i.; Department of Biology of the Cell Nucleus; Prague, Czech Republic.
Sukriye YildirimInstitute of Molecular Genetics ASCR v.v.i.; Department of Biology of the Cell Nucleus; Prague, Czech Republic.
Vlada V PhilimonenkoInstitute of Molecular Genetics ASCR v.v.i.; Department of Biology of the Cell Nucleus; Prague, Czech Republic.
Pavel MarášekInstitute of Molecular Genetics ASCR v.v.i.; Department of Biology of the Cell Nucleus; Prague, Czech Republic.
Enrique CastañoInstitute of Molecular Genetics ASCR v.v.i.; Department of Biology of the Cell Nucleus; Prague, Czech Republic; Biochemistry and Molecular Plant Biology Department; CICY; Mérida, México.
Pavel HozákInstitute of Molecular Genetics ASCR v.v.i.; Department of Biology of the Cell Nucleus; Prague, Czech Republic.
Institute of Molecular Genetics · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To maintain growth and division, cells require a large-scale production of rRNAs which occurs in the nucleolus. Recently, we have shown the interaction of nucleolar phosphatidylinositol 4,5-bisphosphate (PIP2) with proteins involved in rRNA transcription and processing, namely RNA polymerase I (Pol I), UBF, and fibrillarin. Here we extend the study by investigating transcription-related localization of PIP2 in regards to transcription and processing complexes of Pol I. To achieve this, we used either physiological inhibition of transcription during mitosis or inhibition by treatment the cells with actinomycin D (AMD) or 5,6-dichloro-1β-d-ribofuranosyl-benzimidazole (DRB). We show that PIP2 is associated with Pol I subunits and UBF in a transcription-independent manner. On the other hand, PIP2/fibrillarin colocalization is dependent on the production of rRNA. These results indicate that PIP2 is required not only during rRNA production and biogenesis, as we have shown before, but also plays a structural role as an anchor for the Pol I pre-initiation complex during the cell cycle. We suggest that throughout mitosis, PIP2 together with UBF is involved in forming and maintaining the core platform of the rDNA helix structure. Thus we introduce PIP2 as a novel component of the NOR complex, which is further engaged in the renewed rRNA synthesis upon exit from mitosis.

Indexed as

Cell CycleCell Line, TumorCell NucleolusChromosomal Proteins, Non-HistoneDNA, RibosomalHeLa CellsHumansMitosisNucleolus Organizer RegionPol1 Transcription Initiation Complex ProteinsRecombinant ProteinsRNA Polymerase IRNA, RibosomalTranscription, GeneticChromosomal Proteins, Non-HistoneDNA, RibosomalfibrillarinPol1 Transcription Initiation Complex ProteinsRecombinant ProteinsRNA Polymerase IRNA, Ribosomaltranscription factor UBFfibrillarinmitosisnucleolusPIP2RNA polymerase ItranscriptionUBF

Identifiers

PMID24513678
PMCPMC3925692
OpenAlexW1970166862

What OpenQuestion holds

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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.