Evidence map›Paper›PMID 27858508›Full record

ReviewRNA biology2017

Activation of transcription enforces the formation of distinct nuclear bodies in zebrafish embryos.

Patricia Heyn, Hanna Salmonowicz, Jonathan Rodenfels, Karla M Neugebauer

Open access · bronzeAbstract readReview
In one paragraph

Review in RNA biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 46 citations in OpenAlex.

  1. Resolving Sub-Nuclear Architecture from Compartments to Functional Domains.International journal of molecular sciences · 2026
    Review
  2. Female Aging Affects Coilin Pattern in Mouse Cumulus Cells.Journal of developmental biology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. A dual ribosomal system in the zebrafish soma and germline.bioRxiv : the preprint server for biology · 2024
    Article
  7. Review
  8. Article
  9. [Role of Liquid-Liquid Phase Separation in Cell Fate Transition and Diseases].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2023
    Review
  10. Review
  11. Article
  12. Superresolution light microscopy of theMolecular biology of the cell · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Molecular biology of the cell · 2020
    Article
  17. Review
  18. Review
  19. Article
  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

4 authors at 2 institutions in 2 countries.

Patricia Heyna Max Planck Institute of Molecular Cell Biology and Genetics , Dresden , Germany.
Hanna Salmonowicza Max Planck Institute of Molecular Cell Biology and Genetics , Dresden , Germany.ORCID 0000-0002-9444-1039
Jonathan Rodenfelsb Department of Molecular Biophysics & Biochemistry , Yale University , New Haven , CT , USA.
Karla M Neugebauerb Department of Molecular Biophysics & Biochemistry , Yale University , New Haven , CT , USA.ORCID 0000-0002-3835-6761
Max Planck Institute of Molecular Cell Biology and Genetics · DEYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear bodies are cellular compartments that lack lipid bilayers and harbor specific RNAs and proteins. Recent proposals that nuclear bodies form through liquid-liquid phase separation leave the question of how different nuclear bodies maintain their distinct identities unanswered. Here we investigate Cajal bodies (CBs), histone locus bodies (HLBs) and nucleoli - involved in assembly of the splicing machinery, histone mRNA 3' end processing, and rRNA processing, respectively - in the embryos of the zebrafish, Danio rerio. We take advantage of the transcriptional silence of the 1-cell embryo and follow nuclear body appearance as zygotic transcription becomes activated. CBs are present from fertilization onwards, while HLB and nucleolar components formed foci several hours later when histone genes and rDNA became active. HLB formation was blocked by transcription inhibition, suggesting nascent histone transcripts recruit HLB components like U7 snRNP. Surprisingly, we found that U7 base-pairing with nascent histone transcripts was not required for localization to HLBs. Rather, the type of Sm ring assembled on U7 determined its targeting to HLBs or CBs; the spliceosomal Sm ring targeted snRNAs to CBs while the specialized U7 Sm-ring localized to HLBs, demonstrating the contribution of protein constituents to the distinction among nuclear bodies. Thus, nucleolar, HLB, and CB components can mix in early embryogenesis when transcription is naturally or artificially silenced. These data support a model in which transcription of specific gene loci nucleates nuclear body components with high specificity and fidelity to perform distinct regulatory functions.

Indexed as

Transcriptional ActivationAnimalsCell NucleolusChromosomal Proteins, Non-HistoneCoiled BodiesDNA, RibosomalEmbryonic DevelopmentHistonesModels, BiologicalRibonucleoproteins, Small NuclearRibonucleoprotein, U7 Small NuclearRNA, Small NuclearRNA SplicingSpliceosomesZebrafishZygoteChromosomal Proteins, Non-HistoneDNA, RibosomalfibrillarinHistonesRibonucleoproteins, Small NuclearRibonucleoprotein, U7 Small NuclearRNA, Small NuclearCajal bodycoilinfibrillarinhistone locus bodyliquid phase separationzebrafishzygotic genome activation

Identifiers

PMID27858508
PMCPMC5519242
OpenAlexW2553711301

What OpenQuestion holds

Textmetadata
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.