Evidence map›Paper›PMID 24983480›Full record

ArticleInternational journal of molecular sciences2014

Supraspliceosomes at defined functional states portray the pre-assembled nature of the pre-mRNA processing machine in the cell nucleus.

Hani Kotzer-Nevo, Flavia de Lima Alves, Juri Rappsilber, Joseph Sperling, Ruth Sperling

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Nuclear Roles of Spliceosome-Associated microRNAs in Neuronal Cancer Cells.International journal of molecular sciences · 2025
    Article
  2. Article
  3. Npac Regulates Pre-mRNA Splicing in Mouse Embryonic Stem Cells.International journal of molecular sciences · 2024
    Article
  4. Article
  5. Review
  6. The ChloroplastCells · 2021
    Review
  7. Article
  8. Article
  9. A novel role of U1 snRNP: Splice site selection from a distance.Biochimica et biophysica acta. Gene regulatory mechanisms · 2019
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Dual function of C/D box small nucleolar RNAs in rRNA modification and alternative pre-mRNA splicing.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  15. 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 4 institutions in 3 countries.

Hani Kotzer-NevoDepartment of Genetics, the Hebrew University of Jerusalem, Jerusalem 91904, Israel. hanikotzer@hotmail.com.
Flavia de Lima AlvesWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3JR, UK. flaves12@gmail.com.
Juri RappsilberWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3JR, UK. juri.rappsilber@ed.ac.uk.
Joseph SperlingDepartment of Organic Chemistry, the Weizmann Institute of Science, Rehovot 76100, Israel. j.sperling@weizmann.ac.il.
Ruth SperlingDepartment of Genetics, the Hebrew University of Jerusalem, Jerusalem 91904, Israel. Sperling@cc.huji.ac.il.
Hebrew University of Jerusalem · ILTechnische Universität Berlin · DEUniversity of Edinburgh · GBWeizmann Institute of Science · IL

Funding

The Mammalian Cellular Splicing Machine - Structure and FunctionR01GM079549 · NIGMS · HEBREW UNIVERSITY OF JERUSALEM · PI SPERLING, RUTH · 2008 to 2011
$836k
NIGMS NIH HHS R01 GM079549Wellcome Trust 092076Wellcome Trust 103139Wellcome Trust 103139/Z/13/Z
6 · The paper itself

Abstract

When isolated from mammalian cell nuclei, all nuclear pre-mRNAs are packaged in multi-subunit large ribonucleoprotein complexes-supraspliceosomes-composed of four native spliceosomes interconnected by the pre-mRNA. Supraspliceosomes contain all five spliceosomal U snRNPs, together with other splicing factors, and are functional in splicing. Supraspliceosomes studied thus far represent the steady-state population of nuclear pre-mRNAs that were isolated at different stages of the splicing reaction. To analyze specific splicing complexes, here, we affinity purified Pseudomonas aeruginosa phage 7 (PP7)-tagged splicing complexes assembled in vivo on Adenovirus Major Late (AdML) transcripts at specific functional stages, and characterized them using molecular techniques including mass spectrometry. First, we show that these affinity purified splicing complexes assembled on PP7-tagged AdML mRNA or on PP7-tagged AdML pre-mRNA are assembled in supraspliceosomes. Second, similar to the general population of supraspliceosomes, these defined supraspliceosomes populations are assembled with all five U snRNPs at all splicing stages. This study shows that dynamic changes in base-pairing interactions of U snRNA:U snRNA and U snRNA:pre-mRNA that occur in vivo during the splicing reaction do not require changes in U snRNP composition of the supraspliceosome. Furthermore, there is no need to reassemble a native spliceosome for the splicing of each intron, and rearrangements of the interactions will suffice.

Indexed as

AdenoviridaeCell NucleusHeLa CellsHumansLevivirusPseudomonas aeruginosaRibonucleoproteins, Small NuclearRNA, MessengerRNA PrecursorsRNA, ViralSpliceosomesViral ProteinsRibonucleoproteins, Small NuclearRNA, MessengerRNA PrecursorsRNA, ViralViral Proteins

Identifiers

PMID24983480
PMCPMC4139805
OpenAlexW2000017815

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.