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      Transcriptome Analysis of Tomato Flower Pedicel Tissues Reveals Abscission Zone-Specific Modulation of Key Meristem Activity Genes

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          Abstract

          Tomato flower abscises at the anatomically distinct abscission zone that separates the pedicel into basal and apical portions. During abscission, cell separation occurs only at the abscission zone indicating distinctive molecular regulation in its cells. We conducted a transcriptome analysis of tomato pedicel tissues during ethylene promoted abscission. We found that the abscission zone was the most active site with the largest set of differentially expressed genes when compared with basal and apical portions. Gene Ontology analyses revealed enriched transcription regulation and hydrolase activities in the abscission zone. We also demonstrate coordinated responses of hormone and cell wall related genes. Besides, a number of ESTs representing homologs of key Arabidopsis shoot apical meristem activity genes were found to be preferentially expressed in the abscission zone, including WUSCHEL ( WUS), KNAT6, LATERAL ORGAN BOUNDARIES DOMAIN PROTEIN 1( LBD1), and BELL-like homeodomain protein 1 ( BLH1), as well as tomato axillary meristem genes BLIND ( Bl) and LATERAL SUPPRESSOR ( Ls). More interestingly, the homologs of WUS and the potential functional partner OVATE FAMILIY PROTEIN ( OFP) were subsequently down regulated during abscission while Bl and AGL12 were continuously and specifically induced in the abscission zone. The expression patterns of meristem activity genes corroborate the idea that cells of the abscission zone confer meristem-like nature and coincide with the course of abscission and post-abscission cell differentiation. Our data therefore propose a possible regulatory scheme in tomato involving meristem genes that may be required not only for the abscission zone development, but also for abscission.

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          Regulation of floral organ abscission in Arabidopsis thaliana.

          Abscission is a developmental program that results in the active shedding of infected or nonfunctional organs from a plant body. Here, we establish a signaling pathway that controls abscission in Arabidopsis thaliana from ligand, to receptors, to downstream effectors. Loss of function mutations in Inflorescence Deficient in Abscission (IDA), which encodes a predicted secreted small protein, the receptor-like protein kinases HAESA (HAE) and HAESA-like 2 (HSL2), the Mitogen-Activated Protein Kinase Kinase 4 (MKK4) and MKK5, and a dominant-negative form of Mitogen-Activated Protein Kinase 6 (MPK6) in a mpk3 mutant background all have abscission-defective phenotypes. Conversely, expression of constitutively active MKKs rescues the abscission-defective phenotype of hae hsl2 and ida plants. Additionally, in hae hsl2 and ida plants, MAP kinase activity is reduced in the receptacle, the part of the stem that holds the floral organs. Plants overexpressing IDA in a hae hsl2 background have abscission defects, indicating HAE and HSL2 are epistatic to IDA. Taken together, these results suggest that the sequential action of IDA, HAE and HSL2, and a MAP kinase cascade regulates the programmed separation of cells in the abscission zone.
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            Abscission, dehiscence, and other cell separation processes.

            Cell separation is a critical process that takes place throughout the life cycle of a plant. It enables roots to emerge from germinating seeds, cotyledons, and leaves to expand, anthers to dehisce, fruit to ripen, and organs to be shed. The focus of this review is to examine how processes such as abscission and dehiscence are regulated and the ways new research strategies are helping us to understand the mechanisms involved in bringing about a reduction in cell-to-cell adhesion. The opportunities for using this information to manipulate cell separation for the benefit of agriculture and horticulture are evaluated.
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              SQUAMOSA promoter-binding protein-like transcription factors: star players for plant growth and development.

              SQUAMOSA Promoter-Binding Protein-Like (SPL) genes encode plant-specific transcription factors that play important roles in plant phase transition, flower and fruit development, plant architecture, gibberellins signaling, sporogenesis, and response to copper and fungal toxins. In Arabidopsis, many SPL genes are post-transcriptionally regulated by the microRNA (miRNA) miR156, among which AtSPL9 in turn positively regulates the expression of the second miRNA miR172. This miR156-AtSPL9-miR172 regulatory pathway plays critical roles during juvenile to adult leaf development and the miR156-SPLs feedback interaction persists all through the plant development, which may be conserved in other plants. In the present paper, we provide a concise review on the most recent progress in the regulatory mechanisms associated with plant SPL transcription factors, especially in relation to miRNAs. The potential application of these discoveries in agriculture is briefly discussed. © 2010 Institute of Botany, the Chinese Academy of Sciences.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                4 February 2013
                : 8
                : 2
                : e55238
                Affiliations
                [1 ]National Center for Wheat Research, Henan Agricultural University, Zhengzhou, People’s Republic of China
                [2 ]National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Science, MOA Key Lab for Germplasm and Biotechnology, Chinese Academy of Agricultural Sciences (CAAS), Beijing, People’s Republic of China
                [3 ]Key Laboratory of Symbol Computation and Knowledge Engineering of Ministry of Education, College of Computer Science and Technology, Jilin University, Changchun, People’s Republic of China
                UMass, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: LM. Performed the experiments: XW. Analyzed the data: XW DML ALL XLS. Contributed reagents/materials/analysis tools: RZZ YCL LW. Wrote the paper: LM.

                Article
                PONE-D-12-10092
                10.1371/journal.pone.0055238
                3563536
                23390523
                82989ecf-d029-43c6-86e4-6cfd37473184
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 7 April 2012
                : 28 December 2012
                Page count
                Pages: 12
                Funding
                This work is supported in part by Natural Science Foundation of China (number 31070260) and National Transgenic Key project of MOA of China (number 2013ZX08009-001). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Agriculture
                Crops
                Biology
                Computational Biology
                Genomics
                Genome Analysis Tools
                Transcriptomes
                Genetics
                Plant Genetics
                Crop Genetics
                Genomics
                Genome Analysis Tools
                Transcriptomes
                Plant Science
                Plants
                Flowering Plants
                Plant Growth and Development

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