ArticleFrontiers in plant science2017
Subcellular Localization of a Plant Catalase-Phenol Oxidase, AcCATPO, from
Article in Frontiers in plant science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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6 citing papers in PubMed, 22 citations in OpenAlex.
- Investigation of how gate residues in the main channel affect the catalytic activity of Scytalidium thermophilum catalase.Acta crystallographica. Section D, Structural biology · 2024Article
- ROS generated from biotic stress: Effects on plants and alleviation by endophytic microbes.Frontiers in plant science · 2022Review
- Virtual 2-D map of the fungal proteome.Scientific reports · 2021Article
- Abiotic Stress and Reactive Oxygen Species: Generation, Signaling, and Defense Mechanisms.Antioxidants (Basel, Switzerland) · 2021Review
- Reactive oxygen species metabolism and photosynthetic performance in leaves of Hordeum vulgare plants co-infested with Heterodera filipjevi and Aceria tosichella.Plant cell reports · 2020Article
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3 authors at 1 institution in 1 country.
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Abstract
AcCATPO is a plant catalase-phenol oxidase recently identified from red amaranth. Its physiological function remains unexplored. As the starting step of functional analysis, here we report its subcellular localization and a non-canonical targeting signal. Commonly used bioinformatics programs predicted a peroxisomal localization for AcCATPO, but failed in identification of canonical peroxisomal targeting signals (PTS). The C-terminal GFP tagging led the fusion protein AcCATPO-GFP to the cytosol and the nucleus, but N-terminal tagging directed the GFP-AcCATPO to peroxisomes and nuclei, in transgenic tobacco. Deleting the tripeptide (PTM) at the extreme C-terminus almost ruled out the peroxisomal localization of GFP-AcCATPOΔ3, and removing the C-terminal decapeptide completely excluded peroxisomes as the residence of GFP-AcCATPOΔ10. Furthermore, this decapeptide as a targeting signal could import GFP-10aa to the peroxisome exclusively. Taken together, these results demonstrate that AcCATPO is localized to the peroxisome and the nucleus, and its peroxisomal localization is attributed to a non-canonical PTS1, the C-terminal decapeptide which contains an internal SRL motif and a conserved tripeptide P-S/T-I/M at the extreme of C-terminus. This work may further the study as to the physiological function of AcCATPO, especially clarify its involvement in betalain biosynthesis, and provide a clue to elucidate more non-canonic PTS.
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