Evidence map›Paper›PMID 26888869›Full record

ArticleG3 (Bethesda, Md.)2016

Microarray Analysis of Gene Expression in Saccharomyces cerevisiae kap108Δ Mutants upon Addition of Oxidative Stress.

Kenneth D Belanger, Nathaniel Larson, Jonathan Kahn, Dmitry Tkachev, Ahmet Ay

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

5 authors at 1 institution in 1 country.

Kenneth D BelangerDepartment of Biology, Colgate University, Hamilton, New York 13346 kbelanger@colgate.edu.ORCID 0000-0002-7181-0188
Nathaniel LarsonDepartment of Biology, Colgate University, Hamilton, New York 13346.
Jonathan KahnDepartment of Biology, Colgate University, Hamilton, New York 13346.
Dmitry TkachevDepartment of Biology, Colgate University, Hamilton, New York 13346.
Ahmet AyDepartment of Biology, Colgate University, Hamilton, New York 13346 Department of Mathematics, Colgate University, Hamilton, New York 13346.
Colgate University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein transport between the nucleus and cytoplasm of eukaryotic cells is tightly regulated, providing a mechanism for controlling intracellular localization of proteins, and regulating gene expression. In this study, we have investigated the importance of nucleocytoplasmic transport mediated by the karyopherin Kap108 in regulating cellular responses to oxidative stress in Saccharomyces cerevisiae We carried out microarray analyses on wild-type and kap108 mutant cells grown under normal conditions, shortly after introduction of oxidative stress, after 1 hr of oxidative stress, and 1 hr after oxidative stress was removed. We observe more than 500 genes that undergo a 40% or greater change in differential expression between wild-type and kap108Δ cells under at least one of these conditions. Genes undergoing changes in expression can be categorized in two general groups: 1) those that are differentially expressed between wild-type and kap108Δ cells, no matter the oxidative stress conditions; and 2) those that have patterns of response dependent upon both the absence of Kap108, and introduction or removal of oxidative stress. Gene ontology analysis reveals that, among the genes whose expression is reduced in the absence of Kap108 are those involved in stress response and intracellular transport, while those overexpressed are largely involved in mating and pheromone response. We also identified 25 clusters of genes that undergo similar patterns of change in gene expression when oxidative stresses are added and subsequently removed, including genes involved in stress response, oxidation-reduction processing, iron homeostasis, ascospore wall assembly, transmembrane transport, and cell fusion during mating. These data suggest that Kap108 is important for regulating expression of genes involved in a variety of specific cell functions.

Indexed as

Gene Expression Regulation, FungalMutationGene Expression ProfilingKaryopherinsOligonucleotide Array Sequence AnalysisOxidative StressSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsTranscriptomeKaryopherinsSaccharomyces cerevisiae ProteinsSXM1 protein, S cerevisiaegene expressionimportinkaryopherinnuclear transportoxidative stress

Identifiers

PMID26888869
PMCPMC4825647
OpenAlexW2340601760

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.