Evidence map›Paper›PMID 38417553›Full record

ArticleJournal of lipid research2024

Mining cholesterol genes from thousands of mouse livers identifies aldolase C as a regulator of cholesterol biosynthesis.

James A Votava, Steven V John, Zhonggang Li, Shuyang Chen, Jing Fan, Brian W Parks

Open access · goldAbstract read
In one paragraph

Article in Journal of lipid research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Frontiers in endocrinology · 2025
    Article
  7. Article
  8. 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

6 authors at 2 institutions in 1 country.

James A VotavaDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Steven V JohnMorgridge Institute for Research, Madison, WI, USA.
Zhonggang LiDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Shuyang ChenDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA.
Jing FanDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA; Morgridge Institute for Research, Madison, WI, USA.
Brian W ParksDepartment of Nutritional Sciences, University of Wisconsin-Madison, Madison, WI, USA. Electronic address: brian.w.parks@wisc.edu.
University of Wisconsin–Madison · USMorgridge Institute for Research · US

Funding

Metabolic rewiring coupled to the production of reactive oxygen and nitrogen species (RONS)R35GM147014 · NIGMS · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI Jing Fan · 2022 to 2026
$2.1M
Regulation of Cholesterol Metabolism by Sestrin1R01HL147097 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI PARKS, BRIAN WESLEY · 2019 to 2023
$1.9M
NHLBI NIH HHS R01 HL147097NIGMS NIH HHS R35 GM147014
6 · The paper itself

Abstract

The availability of genome-wide transcriptomic and proteomic datasets is ever-increasing and often not used beyond initial publication. Here, we applied module-based coexpression network analysis to a comprehensive catalog of 35 mouse genome-wide liver expression datasets (encompassing more than 3800 mice) with the goal of identifying and validating unknown genes involved in cholesterol metabolism. From these 35 datasets, we identified a conserved module of genes enriched with cholesterol biosynthetic genes. Using a systematic approach across the 35 datasets, we identified three genes (Rdh11, Echdc1, and Aldoc) with no known role in cholesterol metabolism. We then performed functional validation studies and show that each gene is capable of regulating cholesterol metabolism. For the glycolytic gene, Aldoc, we demonstrate that it contributes to de novo cholesterol biosynthesis and regulates cholesterol and triglyceride levels in mice. As Aldoc is located within a genome-wide significant genome-wide association studies locus for human plasma cholesterol levels, our studies establish Aldoc as a causal gene within this locus. Through our work, we develop a framework for leveraging mouse genome-wide liver datasets for identifying and validating genes involved in cholesterol metabolism.

Indexed as

Fructose-Bisphosphate AldolaseGenome-Wide Association StudyAnimalsCholesterolHumansLiverMiceProteomicsCholesterolFructose-Bisphosphate AldolaseALDOCcholesterolECHDC1lipid metabolismRDH11triglyceridesWGCNA

Identifiers

PMID38417553
PMCPMC10965479
OpenAlexW4392234299

What OpenQuestion holds

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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.