Evidence map›Paper›PMID 28686747›Full record

ArticlePloS one2017

Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development.

Anita M Quintana, Jose A Hernandez, Cesar G Gonzalez

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  7. Abnormal chondrocyte intercalation in a zebrafish model ofbioRxiv : the preprint server for biology · 2023
    Article
  8. Article
  9. Review
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  11. Article
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  13. Article
  14. Mutations in the zebrafishBlood advances · 2019
    Article
  15. Article
  16. Review
  17. 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

3 authors at 1 institution in 1 country.

Anita M QuintanaDepartment of Biological Sciences, University of Texas El Paso, El Paso, TX, United States of America.ORCID http://orcid.org/0000-0002-3596-1587
Jose A HernandezDepartment of Biological Sciences, University of Texas El Paso, El Paso, TX, United States of America.
Cesar G GonzalezDepartment of Biological Sciences, University of Texas El Paso, El Paso, TX, United States of America.
The University of Texas at El Paso · US

Funding

TCCG12MD007592 · NIMHD · UNIVERSITY OF TEXAS EL PASO · PI KIRKEN, ROBERT A. · 2012 to 2018
$19.4M
Phase II of BUILDing SCHOLARSUL1GM118970 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI ALEY, STEPHEN B, BOLAND, THOMAS · 2015 to 2023
$17.9M
Development of Psychopathology, Psychobiology, & BehaviorT32MH015442 · NIMH · UNIVERSITY OF COLORADO DENVER · PI JASON R TREGELLAS · 1985 to 2026
$10.2M
Phase II of BUILDing SCHOLARS - Student Training CoreTL4GM118971 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI ALEY, STEPHEN B, BOLAND, THOMAS · 2015 to 2023
$9.9M
Phase II of BUILDing SCHOLARS - Research Enrichment CoreRL5GM118969 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI ALEY, STEPHEN B, BOLAND, THOMAS · 2015 to 2023
$7.4M
Mutations in HCFC1 alter neural precursor differentiationK01NS099153 · NINDS · UNIVERSITY OF TEXAS EL PASO · PI QUINTANA, ANITA M · 2017 to 2019
$701k
NIGMS NIH HHS RL5 GM118969NIGMS NIH HHS TL4 GM118971NIGMS NIH HHS UL1 GM118970NIMHD NIH HHS G12 MD007592NIMH NIH HHS T32 MH015442NINDS NIH HHS K01 NS099153
6 · The paper itself

Abstract

There are 8 different human syndromes caused by mutations in the cholesterol synthesis pathway. A subset of these disorders such as Smith-Lemli-Opitz disorder, are associated with facial dysmorphia. However, the molecular and cellular mechanisms underlying such facial deficits are not fully understood, primarily because of the diverse functions associated with the cholesterol synthesis pathway. Recent evidence has demonstrated that mutation of the zebrafish ortholog of HMGCR results in orofacial clefts. Here we sought to expand upon these data, by deciphering the cholesterol dependent functions of the cholesterol synthesis pathway from the cholesterol independent functions. Moreover, we utilized loss of function analysis and pharmacological inhibition to determine the extent of sonic hedgehog (Shh) signaling in animals with aberrant cholesterol and/or isoprenoid synthesis. Our analysis confirmed that mutation of hmgcs1, which encodes the first enzyme in the cholesterol synthesis pathway, results in craniofacial abnormalities via defects in cranial neural crest cell differentiation. Furthermore targeted pharmacological inhibition of the cholesterol synthesis pathway revealed a novel function for isoprenoid synthesis during vertebrate craniofacial development. Mutation of hmgcs1 had no effect on Shh signaling at 2 and 3 days post fertilization (dpf), but did result in a decrease in the expression of gli1, a known Shh target gene, at 4 dpf, after morphological deficits in craniofacial development and chondrocyte differentiation were observed in hmgcs1 mutants. These data raise the possibility that deficiencies in cholesterol modulate chondrocyte differentiation by a combination of Shh independent and Shh dependent mechanisms. Moreover, our results describe a novel function for isoprenoids in facial development and collectively suggest that cholesterol regulates craniofacial development through versatile mechanisms.

Indexed as

AnimalsAnticholesteremic AgentsAtorvastatinBenzophenonesBody PatterningCell DifferentiationCholesterolChondrocytesCraniofacial AbnormalitiesDibenzocycloheptenesEmbryo, NonmammalianEnzyme InhibitorsGene Expression Regulation, DevelopmentalHedgehog ProteinsHumansHydroxymethylglutaryl CoA ReductasesAnticholesteremic AgentsAtorvastatinBenzophenonesCholesterolDibenzocycloheptenesEnzyme InhibitorsHedgehog ProteinsHMGCS1 protein, humanHydroxymethylglutaryl CoA ReductasesHydroxymethylglutaryl-CoA SynthaselonafarnibPiperidinesPyridinesRo 48-8071Shha protein, zebrafishTerpenesZebrafish ProteinsZinc Finger Protein GLI1

Identifiers

PMID28686747
PMCPMC5501617
OpenAlexW2724449250

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.