Evidence map›Paper›PMID 17180682›Full record

ArticleHistochemistry and cell biology2007

Localization of the pre-squalene segment of the isoprenoid biosynthetic pathway in mammalian peroxisomes.

Werner J Kovacs, Khanichi N Tape, Janis E Shackelford, Xueying Duan, Takhar Kasumov, Joanne K Kelleher, Henri Brunengraber, Skaidrite K Krisans

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Histochemistry and cell biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

41 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Article
  3. Peroxisome Dysfunction and Steatotic Liver Disease.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Peroxisomes: A New Hub for Metabolic Engineering in Yeast.Frontiers in bioengineering and biotechnology · 2021
    Article
  10. Pexophagy: A Model for Selective Autophagy.International journal of molecular sciences · 2020
    Review
  11. Article
  12. Frontiers in microbiology · 2020
    Article
  13. Article
  14. Article
  15. Peroxisomal Dysfunction in Age-Related Diseases.Trends in endocrinology and metabolism: TEM · 2017
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

8 authors at 3 institutions in 1 country.

Werner J KovacsDepartment of Biology, San Diego State University, San Diego, CA, USA. werner.kovacs@anatomie.med.uni-giessen.de
Khanichi N Tape
Janis E Shackelford
Xueying Duan
Takhar Kasumov
Joanne K Kelleher
Henri Brunengraber
Skaidrite K Krisans
San Diego State University · USCase Western Reserve University · USMassachusetts Institute of Technology · 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 DK58238
6 · The paper itself

Abstract

Previous studies have indicated that the early steps in the isoprenoid/cholesterol biosynthetic pathway occur in peroxisomes. However, the role of peroxisomes in cholesterol biosynthesis has recently been questioned in several reports concluding that three of the peroxisomal cholesterol biosynthetic enzymes, namely mevalonate kinase, phosphomevalonate kinase, and mevalonate diphosphate decarboxylase, do not localize to peroxisomes in human cells even though they contain consensus peroxisomal targeting signals. We re-investigated the subcellular localization of the cholesterol biosynthetic enzymes of the pre-squalene segment in human cells by using new stable isotopic techniques and data computations with isotopomer spectral analysis, in combination with immunofluorescence and cell permeabilization techniques. Our present findings clearly show and confirm previous studies that the pre-squalene segment of the cholesterol biosynthetic pathway is localized to peroxisomes. In addition, our data are consistent with the hypothesis that acetyl-CoA derived from peroxisomal beta-oxidation of very long-chain fatty acids and medium-chain dicarboxylic acids is preferentially channeled to cholesterol synthesis inside the peroxisomes without mixing with the cytosolic acetyl-CoA pool.

Indexed as

Acetyl-CoA C-AcetyltransferaseAnimalsCarbon-Carbon Double Bond IsomerasesCarcinoma, HepatocellularCell Line, TumorCell Membrane PermeabilityCHO CellsCholesterolCricetinaeCricetulusDigitoninFatty AcidsFluorescent Antibody Technique, IndirectGeranyltranstransferaseHemiterpenesHumansAcetyl-CoA C-Acetyltransferasebehenic acidCarbon-Carbon Double Bond IsomerasesCholesterolDigitoninFatty AcidsGeranyltranstransferaseHemiterpenesHydroxymethylglutaryl-CoA SynthaseIndicators and Reagentsisopentenyldiphosphate delta-isomerasemevalonate kinasephosphomevalonate kinasePhosphotransferases (Alcohol Group Acceptor)Phosphotransferases (Phosphate Group Acceptor)SqualeneTerpenes

Identifiers

PMID17180682
OpenAlexW2049036844

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.