Evidence map›Paper›PMID 30651636›Full record

ArticleNature2019

Excised linear introns regulate growth in yeast.

Jeffrey T Morgan, Gerald R Fink, David P Bartel

Open access · bronzeAbstract read
In one paragraph

Article in Nature, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

95 citing papers in PubMed, 169 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. The Kinetic Intron Hypothesis.bioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. DecodingbioRxiv : the preprint server for biology · 2025
    Article
  15. Article
  16. Article
  17. Genome-Wide Identification and Expression Analysis ofInternational journal of molecular sciences · 2025
    Article
  18. Article
  19. Frontiers in plant science · 2025
    Article
  20. Article

35 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Jeffrey T MorganHoward Hughes Medical Institute, Cambridge, MA, USA.
Gerald R FinkWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
David P BartelHoward Hughes Medical Institute, Cambridge, MA, USA. dbartel@wi.mit.edu.
Massachusetts Institute of Technology · USHoward Hughes Medical Institute · US

Funding

PRE-DOCTORAL TRAINING IN THE BIOLOGICAL SCIENCEST32GM007287 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BELL, STEPHEN P., KEATING, AMY E · 1985 to 2019
$40.8M
Post-transcriptional gene regulationR35GM118135 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI DAVID P BARTEL · 2016 to 2026
$10.7M
REGULATION OF HISTIDINE BIOSYNTHESIS IN YEASTR01GM035010 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI FINK, GERALD R · 1985 to 2016
$9.9M
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM035010NIGMS NIH HHS R35 GM118135NIGMS NIH HHS T32 GM007287
6 · The paper itself

Abstract

Spliceosomal introns are ubiquitous non-coding RNAs that are typically destined for rapid debranching and degradation. Here we describe 34 excised introns in Saccharomyces cerevisiae that-despite being rapidly degraded in log-phase growth-accumulate as linear RNAs under either saturated-growth conditions or other stresses that cause prolonged inhibition of TORC1, which is a key integrator of growth signalling. Introns that become stabilized remain associated with components of the spliceosome and differ from other spliceosomal introns in having a short distance between their lariat branch point and 3' splice site, which is necessary and sufficient for their stabilization. Deletion of these unusual introns is disadvantageous in saturated conditions and causes aberrantly high growth rates in yeast that are chronically challenged with the TORC1 inhibitor rapamycin. The reintroduction of native or engineered stable introns suppresses this aberrant rapamycin response. Thus, excised introns function within the TOR growth-signalling network of S. cerevisiae and, more generally, excised spliceosomal introns can have biological functions.

Indexed as

ActinsGenes, FungalGenetic FitnessIntronsMechanistic Target of Rapamycin Complex 1Membrane GlycoproteinsMembrane ProteinsMicrofilament ProteinsRNA Splice SitesRNA StabilitySaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSirolimusSpliceosomesAct1 protein, S cerevisiaeActinsECM33 protein, S cerevisiaeMechanistic Target of Rapamycin Complex 1Membrane GlycoproteinsMembrane ProteinsMicrofilament ProteinsplastinRNA Splice SitesSaccharomyces cerevisiae ProteinsSirolimus

Identifiers

PMID30651636
PMCPMC6464110
OpenAlexW2952328530

What OpenQuestion holds

Textmetadata
LicenceTDM
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.