Evidence map›Paper›PMID 31978056›Full record

ArticlePloS one2020

Murine Surf4 is essential for early embryonic development.

Brian T Emmer, Paul J Lascuna, Vi T Tang, Emilee N Kotnik, Thomas L Saunders, Rami Khoriaty, David Ginsburg

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  4. Genetics of hemostasis: from bedside to bench and back again.The Journal of clinical investigation · 2024
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  15. A SURF4-to-proteoglycan relay mechanism that mediates the sorting and secretion of a tagged variant of sonic hedgehog.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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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

7 authors at 2 institutions in 1 country.

Brian T EmmerDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-7365-1021
Paul J LascunaLife Sciences Institute, University of Michigan, Ann Arbor, Michigan.
Vi T TangLife Sciences Institute, University of Michigan, Ann Arbor, Michigan.
Emilee N KotnikLife Sciences Institute, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0002-9229-3378
Thomas L SaundersDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0003-2015-101X
Rami KhoriatyDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
David GinsburgDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
University of Michigan · USHoward Hughes Medical Institute · US

Funding

TRAINING IN MOLECULAR AND CELLULAR CARDIOLOGYT32HL007853 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David J. Pinsky · 1996 to 2026
$11.6M
Institutional Career Development CoreKL2TR002241 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELLINGROD, VICKI L · 2017 to 2021
$6.9M
The molecular pathophysiology of the congenital dyserythropoietic anemiasR01HL148333 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Rami Khoriaty · 2019 to 2026
$4.6M
The Molecular Genetics of HemostasisR35HL135793 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GINSBURG, DAVID · 2017 to 2023
$4.1M
The Evolution of the Mammalian SEC23 Paralogs and the Molecular Pathogenesis of Congenital Dyserythropoietic Anemia type IIK08HL128794 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHORIATY, RAMI · 2015 to 2019
$812k
Cholesterol regulation by the cargo receptor SURF4K08HL148552 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI EMMER, BRIAN T · 2019 to 2023
$788k
Howard Hughes Medical InstituteNCATS NIH HHS KL2 TR002241NHLBI NIH HHS K08 HL128794NHLBI NIH HHS K08 HL148552NHLBI NIH HHS R01 HL148333NHLBI NIH HHS R35 HL135793NHLBI NIH HHS T32 HL007853
6 · The paper itself

Abstract

Newly synthesized proteins co-translationally inserted into the endoplasmic reticulum (ER) lumen may be recruited into anterograde transport vesicles by their association with specific cargo receptors. We recently identified a role for the cargo receptor SURF4 in facilitating the secretion of PCSK9 in cultured cells. To examine the function of SURF4 in vivo, we used CRISPR/Cas9-mediated gene editing to generate mice with germline loss-of-function mutations in Surf4. Heterozygous Surf4+/- mice exhibit grossly normal appearance, behavior, body weight, fecundity, and organ development, with no significant alterations in circulating plasma levels of PCSK9, apolipoprotein B, or total cholesterol, and a detectable accumulation of intrahepatic apoliprotein B. Homozygous Surf4-/- mice exhibit embryonic lethality, with complete loss of all Surf4-/- offspring between embryonic days 3.5 and 9.5. In contrast to the milder murine phenotypes associated with deficiency of known SURF4 cargoes, the embryonic lethality of Surf4-/- mice implies the existence of additional SURF4 cargoes or functions that are essential for murine early embryonic development.

Indexed as

Embryonic DevelopmentAllelesAnimalsApolipoproteins BCholesterolCRISPR-Cas SystemsGene EditingHeterozygoteMembrane ProteinsMiceMice, KnockoutProprotein Convertase 9Apolipoproteins BCholesterolMembrane ProteinsProprotein Convertase 9Surf4 protein, mouse

Identifiers

PMID31978056
PMCPMC6980569
OpenAlexW3002099227

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.