Evidence map›Paper›PMID 12477798›Full record

ArticleEukaryotic cell2002

Loss of compartmentalization causes misregulation of lysine biosynthesis in peroxisome-deficient yeast cells.

Rainer Breitling, Orzala Sharif, Michelle L Hartman, Skaidrite K Krisans

Open access · diamondAbstract read
In one paragraph

Article in Eukaryotic cell, 2002. 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
0.8field-weighted citation impact, top 29% 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, 40 citations in OpenAlex.

  1. Review
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  9. Transforming yeast peroxisomes into microfactories for the efficient production of high-value isoprenoids.Proceedings of the National Academy of Sciences of the United States of America · 2020
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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

4 authors at 1 institution in 1 country.

Rainer BreitlingDepartment of Biology, San Diego State University, San Diego, California 92182, USA.
Orzala Sharif
Michelle L Hartman
Skaidrite K Krisans
San Diego State University · US

Funding

NOVEL GENES OF THE MEVALONATE PATHWAYR01DK058040 · NIDDK · SAN DIEGO STATE UNIVERSITY · PI KRISANS, SKAIDRITE K · 2000 to 2004
$1.8M
Mouse Model for Zellwege SyndromeR01DK058238 · NIDDK · SAN DIEGO STATE UNIVERSITY · PI KRISANS, SKAIDRITE K · 2001 to 2004
$1.1M
NIDDK NIH HHS DK58040NIDDK NIH HHS DK58238NIDDK NIH HHS R01 DK058040NIDDK NIH HHS R01 DK058238
6 · The paper itself

Abstract

To characterize the metabolic role of peroxisomes in yeast cells under physiological conditions, we performed a comprehensive meta-analysis of published microarray data. Previous studies of yeast peroxisomes have mainly been focused on the function of peroxisomes under extreme conditions, such as growth on oleate or methanol as the sole carbon source, and may therefore not be representative of the normal physiological role of yeast peroxisomes. Surprisingly, our analysis of the microarray data reveals that the only pathway responding to peroxisome deficiency in mid-log phase is lysine biosynthesis, whereas classical peroxisomal pathways such as beta-oxidation are unaffected. We show that the upregulation of lysine biosynthesis genes in peroxisome-deficient yeasts shares many characteristics with the physiological response to lysine starvation. We provide data that suggest that this is the result of a "pathological" stimulation of the Lys14p transcriptional activator by the pathway intermediate aminoadipate semialdehyde. Mistargeting of the peroxisomal lysine pathway to the cytosol increases the active concentration of aminoadipate semialdehyde, which is no longer contained in the peroxisome and can now activate Lys14p at much lower levels than in wild-type yeasts. This is the first well-documented example of pathway misregulation in response to peroxisome deficiency and will be useful in understanding the phenotypic details of human peroxisome-deficient patients (Zellweger syndrome).

Indexed as

Biological TransportCytosolDown-RegulationGenome, FungalHumansLysineMembrane ProteinsModels, ChemicalMutationOligonucleotide Array Sequence AnalysisPeroxisomesPhylogenyPromoter Regions, GeneticTranscriptional ActivationTranscription, GeneticUp-RegulationLysineMembrane ProteinsPEX12 protein, human

Identifiers

PMID12477798
PMCPMC138764
OpenAlexW2121838729

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.