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WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana

WHIRLY2 is a single‐stranded DNA binding protein associated with mitochondrial nucleoids. In the why 2‐1 mutant of Arabidopsis thaliana, a major proportion of leaf mitochondria has an aberrant structure characterized by disorganized nucleoids, reduced abundance of cristae, and a low matrix density d...

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Autores principales: Golin, Serena, Negroni, Yuri L., Bennewitz, Bationa, Klösgen, Ralf B., Mulisch, Maria, La Rocca, Nicoletta, Cantele, Francesca, Vigani, Gianpiero, Lo Schiavo, Fiorella, Krupinska, Karin, Zottini, Michela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261051/
https://www.ncbi.nlm.nih.gov/pubmed/32490348
http://dx.doi.org/10.1002/pld3.229
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author Golin, Serena
Negroni, Yuri L.
Bennewitz, Bationa
Klösgen, Ralf B.
Mulisch, Maria
La Rocca, Nicoletta
Cantele, Francesca
Vigani, Gianpiero
Lo Schiavo, Fiorella
Krupinska, Karin
Zottini, Michela
author_facet Golin, Serena
Negroni, Yuri L.
Bennewitz, Bationa
Klösgen, Ralf B.
Mulisch, Maria
La Rocca, Nicoletta
Cantele, Francesca
Vigani, Gianpiero
Lo Schiavo, Fiorella
Krupinska, Karin
Zottini, Michela
author_sort Golin, Serena
collection PubMed
description WHIRLY2 is a single‐stranded DNA binding protein associated with mitochondrial nucleoids. In the why 2‐1 mutant of Arabidopsis thaliana, a major proportion of leaf mitochondria has an aberrant structure characterized by disorganized nucleoids, reduced abundance of cristae, and a low matrix density despite the fact that the macroscopic phenotype during vegetative growth is not different from wild type. These features coincide with an impairment of the functionality and dynamics of mitochondria that have been characterized in detail in wild‐type and why 2‐1 mutant cell cultures. In contrast to the development of the vegetative parts, seed germination is compromised in the why 2‐1 mutant. In line with that, the expression level of why 2 in seeds of wild‐type plants is higher than that of why 3, whereas in adult plant no difference is found. Intriguingly, in early stages of shoots development of the why 2‐1 mutant, although not in seeds, the expression level of why 3 is enhanced. These results suggest that WHIRLY3 is a potential candidate to compensate for the lack of WHIRLY2 in the why 2‐1 mutant. Such compensation is possible only if the two proteins are localized in the same organelle. Indeed, in organello protein transport experiments using intact mitochondria and chloroplasts revealed that WHIRLY3 can be dually targeted into both, chloroplasts and mitochondria. Together, these data indicate that the alterations of mitochondria nucleoids are tightly linked to alterations of mitochondria morphology and functionality. This is even more evident in those phases of plant life when mitochondrial activity is particularly high, such as seed germination. Moreover, our results indicate that the differential expression of why 2 and why 3 predetermines the functional replacement of WHIRLY2 by WHIRLY3, which is restricted though to the vegetative parts of the plant.
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spelling pubmed-72610512020-06-01 WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana Golin, Serena Negroni, Yuri L. Bennewitz, Bationa Klösgen, Ralf B. Mulisch, Maria La Rocca, Nicoletta Cantele, Francesca Vigani, Gianpiero Lo Schiavo, Fiorella Krupinska, Karin Zottini, Michela Plant Direct Original Research WHIRLY2 is a single‐stranded DNA binding protein associated with mitochondrial nucleoids. In the why 2‐1 mutant of Arabidopsis thaliana, a major proportion of leaf mitochondria has an aberrant structure characterized by disorganized nucleoids, reduced abundance of cristae, and a low matrix density despite the fact that the macroscopic phenotype during vegetative growth is not different from wild type. These features coincide with an impairment of the functionality and dynamics of mitochondria that have been characterized in detail in wild‐type and why 2‐1 mutant cell cultures. In contrast to the development of the vegetative parts, seed germination is compromised in the why 2‐1 mutant. In line with that, the expression level of why 2 in seeds of wild‐type plants is higher than that of why 3, whereas in adult plant no difference is found. Intriguingly, in early stages of shoots development of the why 2‐1 mutant, although not in seeds, the expression level of why 3 is enhanced. These results suggest that WHIRLY3 is a potential candidate to compensate for the lack of WHIRLY2 in the why 2‐1 mutant. Such compensation is possible only if the two proteins are localized in the same organelle. Indeed, in organello protein transport experiments using intact mitochondria and chloroplasts revealed that WHIRLY3 can be dually targeted into both, chloroplasts and mitochondria. Together, these data indicate that the alterations of mitochondria nucleoids are tightly linked to alterations of mitochondria morphology and functionality. This is even more evident in those phases of plant life when mitochondrial activity is particularly high, such as seed germination. Moreover, our results indicate that the differential expression of why 2 and why 3 predetermines the functional replacement of WHIRLY2 by WHIRLY3, which is restricted though to the vegetative parts of the plant. John Wiley and Sons Inc. 2020-05-30 /pmc/articles/PMC7261051/ /pubmed/32490348 http://dx.doi.org/10.1002/pld3.229 Text en © 2020 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Golin, Serena
Negroni, Yuri L.
Bennewitz, Bationa
Klösgen, Ralf B.
Mulisch, Maria
La Rocca, Nicoletta
Cantele, Francesca
Vigani, Gianpiero
Lo Schiavo, Fiorella
Krupinska, Karin
Zottini, Michela
WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana
title WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana
title_full WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana
title_fullStr WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana
title_full_unstemmed WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana
title_short WHIRLY2 plays a key role in mitochondria morphology, dynamics, and functionality in Arabidopsis thaliana
title_sort whirly2 plays a key role in mitochondria morphology, dynamics, and functionality in arabidopsis thaliana
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261051/
https://www.ncbi.nlm.nih.gov/pubmed/32490348
http://dx.doi.org/10.1002/pld3.229
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