Evidence map›Paper›PMID 18426585›Full record

ArticleBMC plant biology2008

A spatial dissection of the Arabidopsis floral transcriptome by MPSS.

Jason A Peiffer, Shail Kaushik, Hajime Sakai, Mario Arteaga-Vazquez, Nidia Sanchez-Leon, Hassan Ghazal, Jean-Philippe Vielle-Calzada, Blake C Meyers

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Article in BMC plant biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

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19citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jason A PeifferDepartment of Plant and Soil Sciences, University of Delaware, Newark, DE 19711, USA. jap333@cornell.edu
Shail Kaushik
Hajime Sakai
Mario Arteaga-Vazquez
Nidia Sanchez-Leon
Hassan Ghazal
Jean-Philippe Vielle-Calzada
Blake C Meyers

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

backgroundWe have further characterized floral organ-localized gene expression in the inflorescence of Arabidopsis thaliana by comparison of massively parallel signature sequencing (MPSS) data. Six libraries of RNA sequence tags from immature inflorescence tissues were constructed and matched to their respective loci in the annotated Arabidopsis genome. These signature libraries survey the floral transcriptome of wild-type tissue as well as the floral homeotic mutants, apetala1, apetala3, agamous, a superman/apetala1 double mutant, and differentiated ovules dissected from the gynoecia of wild-type inflorescences. Comparing and contrasting these MPSS floral expression libraries enabled demarcation of transcripts enriched in the petals, stamens, stigma-style, gynoecia, and those with predicted enrichment within the sepal/sepal-petals, petal-stamens, or gynoecia-stamens.

resultsBy comparison of expression libraries, a total of 572 genes were found to have organ-enriched expression within the inflorescence. The bulk of characterized organ-enriched transcript diversity was noted in the gynoecia and stamens, whereas fewer genes demonstrated sepal or petal-localized expression. Validation of the computational analyses was performed by comparison with previously published expression data, in situ hybridizations, promoter-reporter fusions, and reverse transcription PCR. A number of well-characterized genes were accurately delineated within our system of transcript filtration. Moreover, empirical validations confirm MPSS predictions for several genes with previously uncharacterized expression patterns.

conclusionThis extensive MPSS analysis confirms and supplements prior microarray floral expression studies and illustrates the utility of sequence survey-based expression analysis in functional genomics. Spatial floral expression data accrued by MPSS and similar methods will be advantageous in the elucidation of more comprehensive genetic regulatory networks governing floral development.

Indexed as

ArabidopsisFlowersGene Expression ProfilingGene Expression Regulation, PlantGene LibraryGenes, PlantGlucuronidaseImmunohistochemistryIn Situ HybridizationMutationOligonucleotide Array Sequence AnalysisOrgan SpecificityPromoter Regions, GeneticRecombinant Fusion ProteinsReproducibility of ResultsReverse Transcriptase Polymerase Chain ReactionGlucuronidaseRecombinant Fusion Proteins

Identifiers

PMID18426585
PMCPMC2375892

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.