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Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development

We address here organellar genetic regulation and intercompartment genome coordination. We developed earlier a strategy relying on a tRNA-like shuttle to mediate import of nuclear transgene-encoded custom RNAs into mitochondria in plants. In the present work, we used this strategy to drive trans-cle...

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Autores principales: Niazi, Adnan Khan, Delannoy, Etienne, Iqbal, Rana Khalid, Mileshina, Daria, Val, Romain, Gabryelska, Marta, Wyszko, Eliza, Soubigou-Taconnat, Ludivine, Szymanski, Maciej, Barciszewski, Jan, Weber-Lotfi, Frédérique, Gualberto, José Manuel, Dietrich, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627697/
https://www.ncbi.nlm.nih.gov/pubmed/31200566
http://dx.doi.org/10.3390/cells8060583
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author Niazi, Adnan Khan
Delannoy, Etienne
Iqbal, Rana Khalid
Mileshina, Daria
Val, Romain
Gabryelska, Marta
Wyszko, Eliza
Soubigou-Taconnat, Ludivine
Szymanski, Maciej
Barciszewski, Jan
Weber-Lotfi, Frédérique
Gualberto, José Manuel
Dietrich, André
author_facet Niazi, Adnan Khan
Delannoy, Etienne
Iqbal, Rana Khalid
Mileshina, Daria
Val, Romain
Gabryelska, Marta
Wyszko, Eliza
Soubigou-Taconnat, Ludivine
Szymanski, Maciej
Barciszewski, Jan
Weber-Lotfi, Frédérique
Gualberto, José Manuel
Dietrich, André
author_sort Niazi, Adnan Khan
collection PubMed
description We address here organellar genetic regulation and intercompartment genome coordination. We developed earlier a strategy relying on a tRNA-like shuttle to mediate import of nuclear transgene-encoded custom RNAs into mitochondria in plants. In the present work, we used this strategy to drive trans-cleaving hammerhead ribozymes into the organelles, to knock down specific mitochondrial RNAs and analyze the regulatory impact. In a similar approach, the tRNA mimic was used to import into mitochondria in Arabidopsis thaliana the orf77, an RNA associated with cytoplasmic male sterility in maize and possessing sequence identities with the atp9 mitochondrial RNA. In both cases, inducible expression of the transgenes allowed to characterise early regulation and signaling responses triggered by these respective manipulations of the organellar transcriptome. The results imply that the mitochondrial transcriptome is tightly controlled by a “buffering” mechanism at the early and intermediate stages of plant development, a control that is released at later stages. On the other hand, high throughput analyses showed that knocking down a specific mitochondrial mRNA triggered a retrograde signaling and an anterograde nuclear transcriptome response involving a series of transcription factor genes and small RNAs. Our results strongly support transcriptome coordination mechanisms within the organelles and between the organelles and the nucleus.
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spelling pubmed-66276972019-07-23 Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development Niazi, Adnan Khan Delannoy, Etienne Iqbal, Rana Khalid Mileshina, Daria Val, Romain Gabryelska, Marta Wyszko, Eliza Soubigou-Taconnat, Ludivine Szymanski, Maciej Barciszewski, Jan Weber-Lotfi, Frédérique Gualberto, José Manuel Dietrich, André Cells Article We address here organellar genetic regulation and intercompartment genome coordination. We developed earlier a strategy relying on a tRNA-like shuttle to mediate import of nuclear transgene-encoded custom RNAs into mitochondria in plants. In the present work, we used this strategy to drive trans-cleaving hammerhead ribozymes into the organelles, to knock down specific mitochondrial RNAs and analyze the regulatory impact. In a similar approach, the tRNA mimic was used to import into mitochondria in Arabidopsis thaliana the orf77, an RNA associated with cytoplasmic male sterility in maize and possessing sequence identities with the atp9 mitochondrial RNA. In both cases, inducible expression of the transgenes allowed to characterise early regulation and signaling responses triggered by these respective manipulations of the organellar transcriptome. The results imply that the mitochondrial transcriptome is tightly controlled by a “buffering” mechanism at the early and intermediate stages of plant development, a control that is released at later stages. On the other hand, high throughput analyses showed that knocking down a specific mitochondrial mRNA triggered a retrograde signaling and an anterograde nuclear transcriptome response involving a series of transcription factor genes and small RNAs. Our results strongly support transcriptome coordination mechanisms within the organelles and between the organelles and the nucleus. MDPI 2019-06-13 /pmc/articles/PMC6627697/ /pubmed/31200566 http://dx.doi.org/10.3390/cells8060583 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Niazi, Adnan Khan
Delannoy, Etienne
Iqbal, Rana Khalid
Mileshina, Daria
Val, Romain
Gabryelska, Marta
Wyszko, Eliza
Soubigou-Taconnat, Ludivine
Szymanski, Maciej
Barciszewski, Jan
Weber-Lotfi, Frédérique
Gualberto, José Manuel
Dietrich, André
Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development
title Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development
title_full Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development
title_fullStr Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development
title_full_unstemmed Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development
title_short Mitochondrial Transcriptome Control and Intercompartment Cross-Talk During Plant Development
title_sort mitochondrial transcriptome control and intercompartment cross-talk during plant development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627697/
https://www.ncbi.nlm.nih.gov/pubmed/31200566
http://dx.doi.org/10.3390/cells8060583
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