Multi-targeted trehalose-6-phosphate phosphatase I harbors a novel peroxisomal targeting signal 1 and is essential for flowering and development.


Journal

Planta
ISSN: 1432-2048
Titre abrégé: Planta
Pays: Germany
ID NLM: 1250576

Informations de publication

Date de publication:
18 Apr 2020
Historique:
received: 23 02 2020
accepted: 10 04 2020
entrez: 20 4 2020
pubmed: 20 4 2020
medline: 20 1 2021
Statut: epublish

Résumé

This work reveals information about new peroxisomal targeting signals type 1 and identifies trehalose-6-phosphate phosphatase I as multitargeted and is implicated in plant development, reproduction, and stress response. A putative, non-canonical peroxisomal targeting signal type 1 (PTS1) Pro-Arg-Met > was identified in the extreme C-terminus of trehalose-6-phosphate phosphatase (TPP)I. TPP catalyzes the final step of trehalose synthesis, and the enzyme was previously characterized to be nuclear only (Krasensky et al. in Antioxid Redox Signal 21(9):1289-1304, 2014). Here we show that the TPPI C-terminal decapeptide ending with Pro-Arg-Met > or Pro-Lys-Met > can indeed function as a PTS1. Upon transient expression in two plant expression systems, the free C- or N-terminal end led to the full-length TPPI targeting to peroxisomes and plastids, respectively. The nucleus and nucleolus targeting of the full-length TPPI was observed in both cases. The homozygous T-DNA insertion line of TPPI showed a pleiotropic phenotype including smaller leaves, shorter roots, delayed flowering, hypersensitivity to salt, and a sucrose dependent seedling development. Our results identify novel PTS1s, and TPPI as a protein multi-targeted to peroxisomes, plastids, nucleus, and nucleolus. Altogether our findings implicate an essential role for TPPI in development, reproduction, and cell signaling.

Identifiants

pubmed: 32306103
doi: 10.1007/s00425-020-03389-z
pii: 10.1007/s00425-020-03389-z
pmc: PMC7214503
doi:

Substances chimiques

Arabidopsis Proteins 0
Peroxisomal Targeting Signals 0
trehalose-phosphatase EC 3.1.3.12
Phosphoric Monoester Hydrolases EC 3.1.3.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

98

Subventions

Organisme : Norges Forskningsråd
ID : 251310/F20

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Auteurs

Amr R A Kataya (ARA)

Centre for Organelle Research, Faculty of Science and Technology, University of Stavanger, 4036, Stavanger, Norway. amr.kataya@missouri.edu.
Department of Biochemistry, Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, USA. amr.kataya@missouri.edu.

Ahmed Elshobaky (A)

Centre for Organelle Research, Faculty of Science and Technology, University of Stavanger, 4036, Stavanger, Norway.
Botany Department, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt.

Behzad Heidari (B)

Centre for Organelle Research, Faculty of Science and Technology, University of Stavanger, 4036, Stavanger, Norway.
Department of Plant Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran.

Nemie-Feyissa Dugassa (NF)

Centre for Organelle Research, Faculty of Science and Technology, University of Stavanger, 4036, Stavanger, Norway.

Jay J Thelen (JJ)

Department of Biochemistry, Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO, USA.

Cathrine Lillo (C)

Centre for Organelle Research, Faculty of Science and Technology, University of Stavanger, 4036, Stavanger, Norway.

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Classifications MeSH