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The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity

Members of the ubiquitous COX11 (cytochrome c oxidase 11) protein family are involved in copper delivery to the COX complex. In this work, we characterize the Arabidopsis thaliana COX11 homolog (encoded by locus At1g02410). Western blot analyses and confocal microscopy identified Arabidopsis COX11 a...

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Autores principales: Radin, Ivan, Mansilla, Natanael, Rödel, Gerhard, Steinebrunner, Iris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683207/
https://www.ncbi.nlm.nih.gov/pubmed/26734017
http://dx.doi.org/10.3389/fpls.2015.01091
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author Radin, Ivan
Mansilla, Natanael
Rödel, Gerhard
Steinebrunner, Iris
author_facet Radin, Ivan
Mansilla, Natanael
Rödel, Gerhard
Steinebrunner, Iris
author_sort Radin, Ivan
collection PubMed
description Members of the ubiquitous COX11 (cytochrome c oxidase 11) protein family are involved in copper delivery to the COX complex. In this work, we characterize the Arabidopsis thaliana COX11 homolog (encoded by locus At1g02410). Western blot analyses and confocal microscopy identified Arabidopsis COX11 as an integral mitochondrial protein. Despite sharing high sequence and structural similarities, the Arabidopsis COX11 is not able to functionally replace the Saccharomyces cerevisiae COX11 homolog. Nevertheless, further analysis confirmed the hypothesis that Arabidopsis COX11 is essential for COX activity. Disturbance of COX11 expression through knockdown (KD) or overexpression (OE) affected COX activity. In KD lines, the activity was reduced by ~50%, resulting in root growth inhibition, smaller rosettes and leaf curling. In OE lines, the reduction was less pronounced (~80% of the wild type), still resulting in root growth inhibition. Additionally, pollen germination was impaired in COX11 KD and OE plants. This effect on pollen germination can only partially be attributed to COX deficiency and may indicate a possible auxiliary role of COX11 in ROS metabolism. In agreement with its role in energy production, the COX11 promoter is highly active in cells and tissues with high-energy demand for example shoot and root meristems, or vascular tissues of source and sink organs. In COX11 KD lines, the expression of the plasma-membrane copper transporter COPT2 and of several copper chaperones was altered, indicative of a retrograde signaling pathway pertinent to copper homeostasis. Based on our data, we postulate that COX11 is a mitochondrial chaperone, which plays an important role for plant growth and pollen germination as an essential COX complex assembly factor.
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spelling pubmed-46832072016-01-05 The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity Radin, Ivan Mansilla, Natanael Rödel, Gerhard Steinebrunner, Iris Front Plant Sci Plant Science Members of the ubiquitous COX11 (cytochrome c oxidase 11) protein family are involved in copper delivery to the COX complex. In this work, we characterize the Arabidopsis thaliana COX11 homolog (encoded by locus At1g02410). Western blot analyses and confocal microscopy identified Arabidopsis COX11 as an integral mitochondrial protein. Despite sharing high sequence and structural similarities, the Arabidopsis COX11 is not able to functionally replace the Saccharomyces cerevisiae COX11 homolog. Nevertheless, further analysis confirmed the hypothesis that Arabidopsis COX11 is essential for COX activity. Disturbance of COX11 expression through knockdown (KD) or overexpression (OE) affected COX activity. In KD lines, the activity was reduced by ~50%, resulting in root growth inhibition, smaller rosettes and leaf curling. In OE lines, the reduction was less pronounced (~80% of the wild type), still resulting in root growth inhibition. Additionally, pollen germination was impaired in COX11 KD and OE plants. This effect on pollen germination can only partially be attributed to COX deficiency and may indicate a possible auxiliary role of COX11 in ROS metabolism. In agreement with its role in energy production, the COX11 promoter is highly active in cells and tissues with high-energy demand for example shoot and root meristems, or vascular tissues of source and sink organs. In COX11 KD lines, the expression of the plasma-membrane copper transporter COPT2 and of several copper chaperones was altered, indicative of a retrograde signaling pathway pertinent to copper homeostasis. Based on our data, we postulate that COX11 is a mitochondrial chaperone, which plays an important role for plant growth and pollen germination as an essential COX complex assembly factor. Frontiers Media S.A. 2015-12-18 /pmc/articles/PMC4683207/ /pubmed/26734017 http://dx.doi.org/10.3389/fpls.2015.01091 Text en Copyright © 2015 Radin, Mansilla, Rödel and Steinebrunner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Radin, Ivan
Mansilla, Natanael
Rödel, Gerhard
Steinebrunner, Iris
The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity
title The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity
title_full The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity
title_fullStr The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity
title_full_unstemmed The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity
title_short The Arabidopsis COX11 Homolog is Essential for Cytochrome c Oxidase Activity
title_sort arabidopsis cox11 homolog is essential for cytochrome c oxidase activity
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683207/
https://www.ncbi.nlm.nih.gov/pubmed/26734017
http://dx.doi.org/10.3389/fpls.2015.01091
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