Evidence map›Paper›PMID 40205732›Full record

ArticleG3 (Bethesda, Md.)2025

A Saccharomyces cerevisiae knockout screen for genes critical for growth under sulfur- and nitrogen-limited conditions reveals intracellular sorting via vesicular transport systems.

Sean Simmons, Joseph Graham, David Cobb, Shreya Sudakar, Emma G Teng, Emily Lee, Elaine T Do, Logan Scott, Allison Price, Perry Kezh and 1 more

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Sean SimmonsDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Joseph GrahamDepartment of Biology, Mercer University, Macon, GA 31207, USA.
David CobbDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Shreya SudakarDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Emma G TengDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Emily LeeDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Elaine T DoDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Logan ScottDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Allison PriceDepartment of Biology, Mercer University, Macon, GA 31207, USA.
Perry KezhDepartment of Biology, Mercer University, Macon, GA 31207, USA.ORCID 0009-0009-4888-3360
Amy M WilesDepartment of Biology, Mercer University, Macon, GA 31207, USA.ORCID 0000-0002-4171-5278

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is understood that nutrient availability significantly impacts cellular growth and metabolism. The genetic basis for survival in nutrient-limited conditions, however, is not as thoroughly explored. The identification and description of the genes vital for growth in these conditions would therefore enhance the understanding of the signaling and biochemical pathways and processes crucial for cellular survival and growth under these constraints. A growth screen of a gene deletion library representing 4,934 genes of Saccharomyces cerevisiae was completed to discover genes required for normal growth under sulfur- and nitrogen-limited conditions. Genes were identified as required under these restrictive environments based on a comparison with their growth in a synthetic, defined control medium. After normalization and statistical analysis, 732 genes were noted as essential in sulfur-limited medium, and 761 genes were found for nitrogen-limited medium, with an overlap of 313 genes found to be needed in both, significantly more than expected by chance. Kyoto Encyclopedia of Genes and Genomes and Gene Ontologies were analyzed to investigate those processes involved. Proteins identified act in central metabolism and in metabolism of amino acids, glycerolipids, glycerophospholipids, and vitamins and in the pathways of mitogen-activated protein kinase and phosphatidylinositol signaling and the processes of vesicle trafficking, autophagy, mitophagy, and endocytosis. Of these, the metabolism and signaling of phosphatidylinositols are not frequently identified in screens examining nutrient starvation in yeast, nor are vesicular fusion, endocytosis, or trafficking to the early endosome, as we have discovered here. This study invites further exploration into the roles of these processes in adaptation to nutrient stress.

Indexed as

NitrogenSaccharomyces cerevisiaeSulfurTransport VesiclesGene Knockout TechniquesSaccharomyces cerevisiae ProteinsNitrogenSaccharomyces cerevisiae ProteinsSulfurautophagyendosomeintracellular sortingknockout screenlimited nutrientsnitrogenpathway analysisphosphatidylinositolSaccharomyces cerevisiaesulfurvesicular transport

Identifiers

PMID40205732
PMCPMC12239629

What OpenQuestion holds

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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.