Evidence map›Paper›PMID 32118581›Full record

ArticleeLife2020

Enhanced ER-associated degradation of HMG CoA reductase causes embryonic lethality associated with

Youngah Jo, Steven S Kim, Kristina Garland, Iris Fuentes, Lisa M DiCarlo, Jessie L Ellis, Xueyan Fu, Sarah L Booth, Bret M Evers, Russell A DeBose-Boyd

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Allosteric regulation of UBIAD1 trafficking from ER to Golgi revealed by chemical genetic screening.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Post-Translational Regulation of HMG CoA Reductase.Cold Spring Harbor perspectives in biology · 2022
    Review
  4. Article
  5. Article
  6. Vitamin K.Advances in nutrition (Bethesda, Md.) · 2022
    Article
  7. Intracellular Cholesterol Synthesis and Transport.Frontiers in cell and developmental biology · 2022
    Review
  8. Review
  9. Article
  10. Functional study of SCCD pathogenic geneMolecular medicine reports · 2021
    Article
  11. Article
  12. Review
  13. Review
  14. Review
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

10 authors at 2 institutions in 1 country.

Youngah JoDepartment of Molecular Genetics, University of Texas Southwestern Medical, Dallas, United States.ORCID 0000-0001-6779-3891
Steven S KimDepartment of Molecular Genetics, University of Texas Southwestern Medical, Dallas, United States.
Kristina GarlandDepartment of Molecular Genetics, University of Texas Southwestern Medical, Dallas, United States.
Iris FuentesDepartment of Molecular Genetics, University of Texas Southwestern Medical, Dallas, United States.
Lisa M DiCarloDepartment of Molecular Genetics, University of Texas Southwestern Medical, Dallas, United States.
Jessie L EllisCenter at Dallas and Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Somerville, United States.
Xueyan FuCenter at Dallas and Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Somerville, United States.
Sarah L BoothCenter at Dallas and Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Somerville, United States.
Bret M EversDepartment of Pathology, University of Texas Southwestern Medical, Dallas, United States.ORCID 0000-0001-5686-0315
Russell A DeBose-BoydDepartment of Molecular Genetics, University of Texas Southwestern Medical, Dallas, United States.ORCID 0000-0002-7452-5227
The University of Texas Southwestern Medical Center · USTufts University · US

Funding

TRANSCRIPTIONAL REGULATION OF LDL RECEPTOR PROMOTERP01HL020948 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI GOLDSTEIN, JOSEPH L · 1985 to 2021
$103.1M
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 HL020948NIGMS NIH HHS R01 GM134700U.S. Department of Agriculture 58-1950-7-707
6 · The paper itself

Abstract

UbiA prenyltransferase domain-containing protein-1 (UBIAD1) synthesizes the vitamin K subtype menaquinone-4 (MK-4). Previous studies in cultured cells (Schumacher et al., 2015) revealed that UBIAD1 also inhibits endoplasmic reticulum (ER)-associated degradation (ERAD) of ubiquitinated HMG CoA reductase (HMGCR), the rate-limiting enzyme of the mevalonate pathway that produces cholesterol and essential nonsterol isoprenoids. Gene knockout studies were previously attempted to explore the function of UBIAD1 in mice; however, homozygous germ-line elimination of the

Indexed as

AnimalsCRISPR-Associated Protein 9CRISPR-Cas SystemsDimethylallyltranstransferaseEndoplasmic ReticulumFemaleFetal DeathGene EditingGene Knockout TechniquesHydroxymethylglutaryl CoA ReductasesMaleMiceMice, KnockoutCRISPR-Associated Protein 9DimethylallyltranstransferaseHydroxymethylglutaryl CoA ReductasesUbiad1 protein, mousecholesteroldevelopmental biologyembryonic lethalityisoprenoidmousevitamin K

Identifiers

PMID32118581
PMCPMC7069719
OpenAlexW3010338201

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.