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Ethylene-induced differential gene expression during abscission of citrus leaves

The main objective of this work was to identify and classify genes involved in the process of leaf abscission in Clementina de Nules (Citrus clementina Hort. Ex Tan.). A 7 K unigene citrus cDNA microarray containing 12 K spots was used to characterize the transcriptome of the ethylene-induced abscis...

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Autores principales: Agustí, Javier, Merelo, Paz, Cercós, Manuel, Tadeo, Francisco R., Talón, Manuel
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2486473/
https://www.ncbi.nlm.nih.gov/pubmed/18515267
http://dx.doi.org/10.1093/jxb/ern138
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author Agustí, Javier
Merelo, Paz
Cercós, Manuel
Tadeo, Francisco R.
Talón, Manuel
author_facet Agustí, Javier
Merelo, Paz
Cercós, Manuel
Tadeo, Francisco R.
Talón, Manuel
author_sort Agustí, Javier
collection PubMed
description The main objective of this work was to identify and classify genes involved in the process of leaf abscission in Clementina de Nules (Citrus clementina Hort. Ex Tan.). A 7 K unigene citrus cDNA microarray containing 12 K spots was used to characterize the transcriptome of the ethylene-induced abscission process in laminar abscission zone-enriched tissues and the petiole of debladed leaf explants. In these conditions, ethylene induced 100% leaf explant abscission in 72 h while, in air-treated samples, the abscission period started later and took 240 h. Gene expression monitored during the first 36 h of ethylene treatment showed that out of the 12 672 cDNA microarray probes, ethylene differentially induced 725 probes distributed as follows: 216 (29.8%) probes in the laminar abscission zone and 509 (70.2%) in the petiole. Functional MIPS classification and manual annotation of differentially expressed genes highlighted key processes regulating the activation and progress of the cell separation that brings about abscission. These included cell-wall modification, lipid transport, protein biosynthesis and degradation, and differential activation of signal transduction and transcription control pathways. Expression data associated with the petiole indicated the occurrence of a double defensive strategy mediated by the activation of a biochemical programme including scavenging ROS, defence and PR genes, and a physical response mostly based on lignin biosynthesis and deposition. This work identifies new genes probably involved in the onset and development of the leaf abscission process and suggests a different but co-ordinated and complementary role for the laminar abscission zone and the petiole during the process of abscission.
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spelling pubmed-24864732009-02-25 Ethylene-induced differential gene expression during abscission of citrus leaves Agustí, Javier Merelo, Paz Cercós, Manuel Tadeo, Francisco R. Talón, Manuel J Exp Bot Research Papers The main objective of this work was to identify and classify genes involved in the process of leaf abscission in Clementina de Nules (Citrus clementina Hort. Ex Tan.). A 7 K unigene citrus cDNA microarray containing 12 K spots was used to characterize the transcriptome of the ethylene-induced abscission process in laminar abscission zone-enriched tissues and the petiole of debladed leaf explants. In these conditions, ethylene induced 100% leaf explant abscission in 72 h while, in air-treated samples, the abscission period started later and took 240 h. Gene expression monitored during the first 36 h of ethylene treatment showed that out of the 12 672 cDNA microarray probes, ethylene differentially induced 725 probes distributed as follows: 216 (29.8%) probes in the laminar abscission zone and 509 (70.2%) in the petiole. Functional MIPS classification and manual annotation of differentially expressed genes highlighted key processes regulating the activation and progress of the cell separation that brings about abscission. These included cell-wall modification, lipid transport, protein biosynthesis and degradation, and differential activation of signal transduction and transcription control pathways. Expression data associated with the petiole indicated the occurrence of a double defensive strategy mediated by the activation of a biochemical programme including scavenging ROS, defence and PR genes, and a physical response mostly based on lignin biosynthesis and deposition. This work identifies new genes probably involved in the onset and development of the leaf abscission process and suggests a different but co-ordinated and complementary role for the laminar abscission zone and the petiole during the process of abscission. Oxford University Press 2008-07 2008-05-29 /pmc/articles/PMC2486473/ /pubmed/18515267 http://dx.doi.org/10.1093/jxb/ern138 Text en © 2008 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)
spellingShingle Research Papers
Agustí, Javier
Merelo, Paz
Cercós, Manuel
Tadeo, Francisco R.
Talón, Manuel
Ethylene-induced differential gene expression during abscission of citrus leaves
title Ethylene-induced differential gene expression during abscission of citrus leaves
title_full Ethylene-induced differential gene expression during abscission of citrus leaves
title_fullStr Ethylene-induced differential gene expression during abscission of citrus leaves
title_full_unstemmed Ethylene-induced differential gene expression during abscission of citrus leaves
title_short Ethylene-induced differential gene expression during abscission of citrus leaves
title_sort ethylene-induced differential gene expression during abscission of citrus leaves
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2486473/
https://www.ncbi.nlm.nih.gov/pubmed/18515267
http://dx.doi.org/10.1093/jxb/ern138
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