Evidence map›Paper›PMID 25795416›Full record

ArticleRNA (New York, N.Y.)2015

Both the autophagy and proteasomal pathways facilitate the Ubp3p-dependent depletion of a subset of translation and RNA turnover factors during nitrogen starvation in Saccharomyces cerevisiae.

Shane P Kelly, David M Bedwell

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

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  15. On the edge of degradation: Autophagy regulation by RNA decay.Wiley interdisciplinary reviews. RNA · 2019
    Review
  16. Distinct segregation patterns of yeast cell-peripheral proteins uncovered by a method for protein segregatome analysis.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Activation of autophagy rescues synaptic and cognitive deficits in fragile X mice.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Article
  19. Article
  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

2 authors at 2 institutions in 1 country.

Shane P KellyDepartment of Cell, Developmental and Integrative Biology, Birmingham, Alabama 35294, USA.
David M BedwellDepartment of Cell, Developmental and Integrative Biology, Birmingham, Alabama 35294, USA Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
American Sports Medicine Institute · USUniversity of Alabama at Birmingham · US

Funding

Mechanism of Eukaryotic Translation TerminationR01GM068854 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BEDWELL, DAVID M. · 2003 to 2011
$2.5M
NIGMS NIH HHS GM068854NIGMS NIH HHS R01 GM068854
6 · The paper itself

Abstract

Protein turnover is an important regulatory mechanism that facilitates cellular adaptation to changing environmental conditions. Previous studies have shown that ribosome abundance is reduced during nitrogen starvation by a selective autophagy mechanism termed ribophagy, which is dependent upon the deubiquitinase Ubp3p. In this study, we asked whether the abundance of various translation and RNA turnover factors are reduced following the onset of nitrogen starvation in Saccharomyces cerevisiae. We found distinct differences in the abundance of the proteins tested following nitrogen starvation: (1) The level of some did not change; (2) others were reduced with kinetics similar to ribophagy, and (3) a few proteins were rapidly depleted. Furthermore, different pathways differentially degraded the various proteins upon nitrogen starvation. The translation factors eRF3 and eIF4GI, and the decapping enhancer Pat1p, required an intact autophagy pathway for their depletion. In contrast, the deadenylase subunit Pop2p and the decapping enzyme Dcp2p were rapidly depleted by a proteasome-dependent mechanism. The proteasome-dependent depletion of Dcp2p and Pop2p was also induced by rapamycin, suggesting that the TOR1 pathway influences this pathway. Like ribophagy, depletion of eIF4GI, eRF3, Dcp2p, and Pop2p was dependent upon Ubp3p to varying extents. Together, our results suggest that the autophagy and proteasomal pathways degrade distinct translation and RNA turnover factors in a Ubp3p-dependent manner during nitrogen starvation. While ribophagy is thought to mediate the reutilization of scarce resources during nutrient limitation, our results suggest that the selective degradation of specific proteins could also facilitate a broader reprogramming of the post-transcriptional control of gene expression.

Indexed as

AutophagySaccharomyces cerevisiaeEndopeptidasesEndoribonucleasesMetabolic Networks and PathwaysNitrogenProteasome Endopeptidase ComplexProtein BiosynthesisProteolysisRibonucleasesRNA, FungalRNA Processing, Post-TranscriptionalRNA StabilitySaccharomyces cerevisiae ProteinsTranscription FactorsDCP2 protein, S cerevisiaeEndopeptidasesEndoribonucleasesNitrogenPOP2 protein, S cerevisiaeProteasome Endopeptidase ComplexRibonucleasesRNA, FungalSaccharomyces cerevisiae ProteinsTranscription FactorsUBP3 protein, S cerevisiaeautophagynitrogen starvationproteasomeRNA turnover factorstranslation factors

Identifiers

PMID25795416
PMCPMC4408797
OpenAlexW2123388104

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.