Evidence map›Paper›PMID 27506241›Full record

ArticlePlant physiology2016

ORM Expression Alters Sphingolipid Homeostasis and Differentially Affects Ceramide Synthase Activity.

Athen N Kimberlin, Gongshe Han, Kyle D Luttgeharm, Ming Chen, Rebecca E Cahoon, Julie M Stone, Jennifer E Markham, Teresa M Dunn, Edgar B Cahoon

Open access · bronzeAbstract read
In one paragraph

Article in Plant physiology, 2016. 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
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. ORMDL Proteins Turnover via Proteasome and Autophagy Is Cell-Type Dependent and Tied to Ceramide Homeostasis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  19. Orm/ORMDL proteins: Gate guardians and master regulators.Advances in biological regulation · 2018
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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

9 authors at 2 institutions in 1 country.

Athen N KimberlinCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.).
Gongshe HanCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.).ORCID 0000-0001-9927-7939
Kyle D LuttgeharmCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.).ORCID 0000-0002-1500-9855
Ming ChenCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.).
Rebecca E CahoonCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.).ORCID 0000-0003-3392-5766
Julie M StoneCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.).ORCID 0000-0003-2829-8569
Jennifer E MarkhamCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.).ORCID 0000-0003-2397-3131
Teresa M DunnCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.) teresa.dunn@usuhs.edu ecahoon2@unl.edu.
Edgar B CahoonCenter for Plant Science Innovation and Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588 (A.N.K., K.D.L., M.C., R.E.C., J.M.S., J.E.M., E.B.C.); andDepartment of Biochemistry and Molecular Biology, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814 (G.H., T.M.D.) teresa.dunn@usuhs.edu ecahoon2@unl.edu.ORCID 0000-0002-7277-1176
University of Nebraska–Lincoln · USUniformed Services University of the Health Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingolipid synthesis is tightly regulated in eukaryotes. This regulation in plants ensures sufficient sphingolipids to support growth while limiting the accumulation of sphingolipid metabolites that induce programmed cell death. Serine palmitoyltransferase (SPT) catalyzes the first step in sphingolipid biosynthesis and is considered the primary sphingolipid homeostatic regulatory point. In this report, Arabidopsis (Arabidopsis thaliana) putative SPT regulatory proteins, orosomucoid-like proteins AtORM1 and AtORM2, were found to interact physically with Arabidopsis SPT and to suppress SPT activity when coexpressed with Arabidopsis SPT subunits long-chain base1 (LCB1) and LCB2 and the small subunit of SPT in a yeast (Saccharomyces cerevisiae) SPT-deficient mutant. Consistent with a role in SPT suppression, AtORM1 and AtORM2 overexpression lines displayed increased resistance to the programmed cell death-inducing mycotoxin fumonisin B

Indexed as

HomeostasisArabidopsisArabidopsis ProteinsGene Expression Regulation, PlantMutationOxidoreductasesPlants, Genetically ModifiedProtein BindingReverse Transcriptase Polymerase Chain ReactionRNA InterferenceSerine C-PalmitoyltransferaseSphingolipidsArabidopsis Proteinsdihydroceramide desaturaseOxidoreductasesSerine C-PalmitoyltransferaseSphingolipids

Identifiers

PMID27506241
PMCPMC5047106
OpenAlexW2509342572

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.