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Patterns of gene expression during Arabidopsis flower development from the time of initiation to maturation.
Ryan, Patrick T; Ó'Maoiléidigh, Diarmuid S; Drost, Hajk-Georg; Kwasniewska, Kamila; Gabel, Alexander; Grosse, Ivo; Graciet, Emmanuelle; Quint, Marcel; Wellmer, Frank.
Afiliação
  • Ryan PT; Smurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland.
  • Ó'Maoiléidigh DS; Smurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland.
  • Drost HG; Present address: Max Planck Institute for Plant Breeding Research, D-50829, Cologne, Germany.
  • Kwasniewska K; Institute of Computer Science, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
  • Gabel A; Smurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland.
  • Grosse I; Institute of Computer Science, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
  • Graciet E; Institute of Computer Science, Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
  • Quint M; Smurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland.
  • Wellmer F; Department of Biology, National University of Ireland Maynooth, Maynooth, Ireland.
BMC Genomics ; 16: 488, 2015 Jul 01.
Article em En | MEDLINE | ID: mdl-26126740
ABSTRACT

BACKGROUND:

The formation of flowers is one of the main model systems to elucidate the molecular mechanisms that control developmental processes in plants. Although several studies have explored gene expression during flower development in the model plant Arabidopsis thaliana on a genome-wide scale, a continuous series of expression data from the earliest floral stages until maturation has been lacking. Here, we used a floral induction system to close this information gap and to generate a reference dataset for stage-specific gene expression during flower formation.

RESULTS:

Using a floral induction system, we collected floral buds at 14 different stages from the time of initiation until maturation. Using whole-genome microarray analysis, we identified 7,405 genes that exhibit rapid expression changes during flower development. These genes comprise many known floral regulators and we found that the expression profiles for these regulators match their known expression patterns, thus validating the dataset. We analyzed groups of co-expressed genes for over-represented cellular and developmental functions through Gene Ontology analysis and found that they could be assigned specific patterns of activities, which are in agreement with the progression of flower development. Furthermore, by mapping binding sites of floral organ identity factors onto our dataset, we were able to identify gene groups that are likely predominantly under control of these transcriptional regulators. We further found that the distribution of paralogs among groups of co-expressed genes varies considerably, with genes expressed predominantly at early and intermediate stages of flower development showing the highest proportion of such genes.

CONCLUSIONS:

Our results highlight and describe the dynamic expression changes undergone by a large number of genes during flower development. They further provide a comprehensive reference dataset for temporal gene expression during flower formation and we demonstrate that it can be used to integrate data from other genomics approaches such as genome-wide localization studies of transcription factor binding sites.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arabidopsis / Perfilação da Expressão Gênica / Proteínas de Arabidopsis / Flores Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arabidopsis / Perfilação da Expressão Gênica / Proteínas de Arabidopsis / Flores Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2015 Tipo de documento: Article