Mouse Fat-Specific Protein 27 (FSP27) expressed in plant cells localizes to lipid droplets and promotes lipid droplet accumulation and fusion.


Journal

Biochimie
ISSN: 1638-6183
Titre abrégé: Biochimie
Pays: France
ID NLM: 1264604

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 21 05 2019
accepted: 05 08 2019
pubmed: 11 8 2019
medline: 26 9 2020
entrez: 11 8 2019
Statut: ppublish

Résumé

Fat-Specific Protein 27 (FSP27) belongs to a small group of vertebrate proteins containing a Cell-death Inducing DNA fragmentation factor-α-like Effector (CIDE)-C domain and is involved in lipid droplet (LD) accumulation and energy homeostasis. FSP27 is predominantly expressed in white and brown adipose tissues, as well as liver, and plays a key role in mediating LD-LD fusion. No orthologs have been identified in invertebrates or plants. In this study, we tested the function of mouse FSP27 in stably-transformed Arabidopsis thaliana leaves and seeds, as well as through transient expression in Nicotiana tabacum suspension-cultured cells and N. benthamiana leaves. Confocal microscopic analysis of plant cells revealed that, similar to ectopic expression in mammalian cells, FSP27 produced in plants 1) correctly localized to LDs, 2) accumulated at LD-LD contact sites, and 3) induced an increase in the number and size of LDs and also promoted LD clustering and fusion. Furthermore, FSP27 increased oil content in transgenic A. thaliana seeds. Given that plant oils have uses in human and animal nutrition as well as industrial uses such as biofuels and bioplastics, our results suggest that ectopic expression of FSP27 in plants represents a potential strategy for increasing oil content and energy density in bioenergy or oilseed crops.

Identifiants

pubmed: 31400447
pii: S0300-9084(19)30234-2
doi: 10.1016/j.biochi.2019.08.002
pii:
doi:

Substances chimiques

Proteins 0
Recombinant Proteins 0
fat-specific protein 27, mouse 0
DGAT2 protein, mouse EC 2.3.1.20
Diacylglycerol O-Acyltransferase EC 2.3.1.20

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

41-53

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK101711
Pays : United States
Organisme : NIDDK NIH HHS
ID : R56 DK094815
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier B.V. and Société Française de Biochimie et Biologie Moléculaire (SFBBM). All rights reserved.

Auteurs

Ann M Price (AM)

BioDiscovery Institute, Department of Biological Sciences, University of North Texas, Denton, TX, USA.

Nathan M Doner (NM)

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.

Satinder K Gidda (SK)

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.

Srikarthika Jambunathan (S)

Department of Medicine, Section of Endocrinology, Diabetes and Nutrition, Boston University School of Medicine, Boston, MA, USA.

Christopher N James (CN)

BioDiscovery Institute, Department of Biological Sciences, University of North Texas, Denton, TX, USA.

Alyssa Schami (A)

BioDiscovery Institute, Department of Biological Sciences, University of North Texas, Denton, TX, USA.

Olga Yurchenko (O)

USDA-ARS, US Arid-Land Agricultural Research Center, Maricopa, AZ, USA.

Robert T Mullen (RT)

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.

John M Dyer (JM)

USDA-ARS, US Arid-Land Agricultural Research Center, Maricopa, AZ, USA.

Vishwajeet Puri (V)

Department of Biomedical Sciences and the Diabetes Institute, Ohio University, Athens, OH, USA.

Kent D Chapman (KD)

BioDiscovery Institute, Department of Biological Sciences, University of North Texas, Denton, TX, USA. Electronic address: chapman@unt.edu.

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Classifications MeSH