Evidence map›Paper›PMID 35940903›Full record

ReviewCold Spring Harbor perspectives in biology2022

Post-Translational Regulation of HMG CoA Reductase.

Youngah Jo, Russell A DeBose-Boyd

Open access · greenAbstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in biology, 2022. 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
–field-weighted citation impact
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, 31 citations in OpenAlex.

  1. Article
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  16. Review
  17. Identification of a depupylation regulator for an essential enzyme inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  18. The cell biology of ferroptosis.Nature reviews. Molecular cell biology · 2024
    Review
  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

2 authors at 2 institutions in 1 country.

Youngah JoDepartment of Molecular Genetics, UT Southwestern Medical Center, Dallas, Texas 75390-9046, USA.
Russell A DeBose-BoydDepartment of Molecular Genetics, UT Southwestern Medical Center, Dallas, Texas 75390-9046, USA.
Southwestern Medical CenterThe University of Texas Southwestern Medical Center · US

Funding

TRANSCRIPTIONAL REGULATION OF LDL RECEPTOR PROMOTERP01HL020948 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI GOLDSTEIN, JOSEPH L · 1985 to 2021
$103.1M
UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeff G McDonald · 2022 to 2026
$7.4M
Significance of UBIAD1 in Regulation of HMG CoA Reductase Degradation, Mevalonate Metabolism, and Menaquinone-4 SynthesisR01GM144039 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI BOOTH, SARAH LOUISE, DEBOSE-BOYD, RUSSELL ALFRED · 2021 to 2024
$1.9M
Examining Mechanism and Physiological Significance of HMG CoA Reductase ER-Associated DegradationR01GM134700 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI DEBOSE-BOYD, RUSSELL ALFRED, LI, XIAOCHUN · 2019 to 2022
$1.7M
NHLBI NIH HHS P01 HL020948NIDDK NIH HHS P30 DK127984NIGMS NIH HHS R01 GM134700NIGMS NIH HHS R01 GM144039
6 · The paper itself

Abstract

3-Hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) is an endoplasmic reticulum (ER)-localized integral membrane protein that catalyzes the rate-limiting step in the synthesis of cholesterol and many nonsterol isoprenoids including geranylgeranyl pyrophosphate (GGpp). HMGCR is subjected to strict feedback control through multiple mechanisms to ensure cells constantly produce essential nonsterol isoprenoids, but do not overaccumulate cholesterol. Here, we focus on the mechanism of feedback control of HMGCR that involves its sterol-induced ubiquitination and ER-associated degradation (ERAD) that is augmented by GGpp. We will also discuss the how GGpp-regulated intracellular trafficking of the vitamin K2 synthetic enzyme UbiA prenyltransferase domain-containing protein-1 (UBIAD1) inhibits HMGCR ERAD to balance the synthesis of sterol and nonsterol isoprenoids. Finally, we will summarize various mouse models, the characterization of which establish that sterol-accelerated, UBIAD1-modulated ERAD plays a major role in regulation of HMGCR and cholesterol metabolism in vivo.

Indexed as

DimethylallyltranstransferaseHydroxymethylglutaryl CoA ReductasesAnimalsCholesterolEndoplasmic Reticulum-Associated DegradationMicePolyisoprenyl PhosphatesSterolsTerpenesCholesterolDimethylallyltranstransferasegeranylgeranyl pyrophosphateHydroxymethylglutaryl CoA ReductasesPolyisoprenyl PhosphatesSterolsTerpenesUbiad1 protein, mouse

Identifiers

PMID35940903
PMCPMC9732902
OpenAlexW4292283991

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.