Evidence map›Paper›PMID 24097436›Full record

ArticleNucleic acids research2014

Cotranscriptional recruitment of yeast TRAMP complex to intronic sequences promotes optimal pre-mRNA splicing.

Ka-Yiu Edwin Kong, Hei-Man Vincent Tang, Kewu Pan, Zhe Huang, Tsz-Hang Jimmy Lee, Alan G Hinnebusch, Dong-Yan Jin, Chi-Ming Wong

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
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  11. The regulation and functions of the nuclear RNA exosome complex.Nature reviews. Molecular cell biology · 2016
    Review
  12. Article
  13. Article
  14. Review
  15. Article
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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

8 authors at 3 institutions in 2 countries.

Ka-Yiu Edwin KongDepartment of Biochemistry, Department of Medicine, State Key Laboratory of Pharmaceutical Biotechnology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 21 Sassoon Road, Pokfulam, Hong Kong and Laboratory of Gene Regulation and Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Hei-Man Vincent Tang
Kewu Pan
Zhe Huang
Tsz-Hang Jimmy Lee
Alan G Hinnebusch
Dong-Yan Jin
Chi-Ming Wong
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USNational Institutes of Health · USUniversity of Hong Kong · HK

Funding

Transcriptional Regulation of Gene ExpressionZIAHD008899 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI HINNEBUSCH, ALAN G · 2010 to 2025
$11.6M
Regulation of transcription termination and its link in mRNA surveillanceR01TW008298 · FIC · UNIVERSITY OF HONG KONG · PI WONG, CHI-MING · 2011 to 2015
$264k
FIC NIH HHS 1R01TW00829801A1FIC NIH HHS R01 TW008298Intramural NIH HHS
6 · The paper itself

Abstract

Most unwanted RNA transcripts in the nucleus of eukaryotic cells, such as splicing-defective pre-mRNAs and spliced-out introns, are rapidly degraded by the nuclear exosome. In budding yeast, a number of these unwanted RNA transcripts, including spliced-out introns, are first recognized by the nuclear exosome cofactor Trf4/5p-Air1/2p-Mtr4p polyadenylation (TRAMP) complex before subsequent nuclear-exosome-mediated degradation. However, it remains unclear when spliced-out introns are recognized by TRAMP, and whether TRAMP may have any potential roles in pre-mRNA splicing. Here, we demonstrated that TRAMP is cotranscriptionally recruited to nascent RNA transcripts, with particular enrichment at intronic sequences. Deletion of TRAMP components led to further accumulation of unspliced pre-mRNAs even in a yeast strain defective in nuclear exosome activity, suggesting a novel stimulatory role of TRAMP in splicing. We also uncovered new genetic and physical interactions between TRAMP and several splicing factors, and further showed that TRAMP is required for optimal recruitment of the splicing factor Msl5p. Our study provided the first evidence that TRAMP facilitates pre-mRNA splicing, and we interpreted this as a fail-safe mechanism to ensure the cotranscriptional recruitment of TRAMP before or during splicing to prepare for the subsequent targeting of spliced-out introns to rapid degradation by the nuclear exosome.

Indexed as

IntronsRNA SplicingAdaptor Proteins, Signal Transducingbeta-GalactosidaseDEAD-box RNA HelicasesDNA-Directed DNA PolymeraseExosome Multienzyme Ribonuclease ComplexGene DeletionGenes, ReporterRibonucleoproteinsRibonucleoprotein, U2 Small NuclearRNA-Binding ProteinsRNA, MessengerRNA PrecursorsRNA, Small NuclearRNA Splicing FactorsAdaptor Proteins, Signal TransducingAir1 protein, S cerevisiaeAir2 protein, S cerevisiaebeta-GalactosidaseDEAD-box RNA HelicasesDNA-Directed DNA PolymeraseExosome Multienzyme Ribonuclease ComplexMSL1 protein, S cerevisiaeMSL5 protein, S cerevisiaeMTR4 protein, S cerevisiaeMUD2 protein, S cerevisiaePAP2 protein, S cerevisiaeRibonucleoproteinsRibonucleoprotein, U2 Small NuclearRNA-Binding ProteinsRNA, MessengerRNA PrecursorsRNA, Small NuclearRNA Splicing FactorsRRP6 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsSplicing Factor U2AF

Identifiers

PMID24097436
PMCPMC3874199
OpenAlexW2044572367

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.