Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1491
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dc.contributor.authorKumari, Aprajita-
dc.contributor.authorKaladhar, Vemula Chandra-
dc.contributor.authorYadav, Nidhi-
dc.contributor.authorSingh, Pooja-
dc.contributor.authorReddy, Kishorekumar-
dc.contributor.authorGupta, Kapuganti Jagadis-
dc.date.accessioned2023-07-05T05:37:40Z-
dc.date.available2023-07-05T05:37:40Z-
dc.date.issued2023-
dc.identifier.citationPlant, Cell & Environment, 46(8): 2492-2506en_US
dc.identifier.issn0140-7791-
dc.identifier.issn1365-3040-
dc.identifier.otherhttps://doi.org/10.1111/pce.14637-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/pce.14637-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1491-
dc.descriptionAccepted date: 25 May 2023en_US
dc.description.abstractThe site of nitric oxide (NO) production in mitochondrial cytochrome c oxidase and the role of NO in mitochondrial biogenesis are not known in plants. By imposing osmotic stress and recovery on Arabidopsis seedlings we investigated the site of NO production and its role in mitochondrial biogenesis. Osmotic stress reduced growth and mitochondrial number while increasing NO production. During the recovery phase the mitochondrial number increased and this increase was higher in wild type and the high NO-producing Pgb1 silencing line in comparison to the NO-deficient nitrate reductase double mutant (nia1/nia2). Application of nitrite stimulated NO production and mitochondrial number in the nia1/nia2 mutant. Osmotic stress induced COX6b−3 and COA6-L genes encoding subunits of COX. The mutants cox6b-3 and coa6-l were impaired both in NO production and mitochondrial number during stress to recovery suggesting the involvement of these subunits in nitrite-dependent NO production. Transcripts encoding the mitochondrial protein import machinery showed reduced expression in cox6b-3 and coa6-l mutants. Finally, COX6b-3 and COA6-L interacted with the VQ27 motif-containing protein in the presence of NO. The vq27 mutant was impaired in mitochondrial biogenesis. Our results suggest the involvement of COX derived NO in mitochondrial biogenesis.en_US
dc.description.sponsorshipWe thank R.G. Ratcliffe, Department of Biology, University of Oxford for a critical reading of the manuscript. We also thank Anupamaa Goyal for assisting in experiments. This work was supported by Science and Engineering Research Board, DBT‐RRSFP‐SAHAJ, BT/ INF/22/SP45162/2021, SERB Core grant CRG/2019/004534, and Indo‐Swiss grant BT/IN/SWISS/47/JGK/2018‐2019 from the Department of Biotechnology, Government of India. PS acknowledges a Senior Research Fellowship from University Grants Commission. NY acknowledge Junior Research Fellowship from University Grants Comission.en_US
dc.language.isoen_USen_US
dc.publisherJohn Wiley & Sonsen_US
dc.subjectcytochrome c oxidaseen_US
dc.subjectmitochondriaen_US
dc.subjectnitrate reductaseen_US
dc.subjectnitriteen_US
dc.subjectphytoglobinen_US
dc.titleNitric oxide regulates mitochondrial biogenesis in plantsen_US
dc.typeArticleen_US
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