BMC Genomics

official impact factor 4.21

Open Access Highly Access Research article

Microarray expression analysis of meiosis and microsporogenesis in hexaploid bread wheat

Wayne Crismani1, Ute Baumann2, Tim Sutton2, Neil Shirley2, Tracie Webster3, German Spangenberg3, Peter Langridge2 and Jason A Able1*

Author Affiliations

1 Molecular Plant Breeding Cooperative Research Centre, School of Agriculture, Food and Wine, The University of Adelaide, Waite Campus, PMB1, Glen Osmond, South Australia, 5064, Australia

2 Australian Centre for Plant Functional Genomics, School of Agriculture, Food and Wine, The University of Adelaide, Waite Campus, PMB1, Glen Osmond, South Australia, 5064, Australia

3 Molecular Plant Breeding Cooperative Research Centre and Australian Centre for Plant Functional Genomics, Victorian AgriBiosciences Centre, La Trobe University, 1 Park Drive, Bundoora, Victoria, 3083, Australia

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BMC Genomics 2006, 7:267 doi:10.1186/1471-2164-7-267

Published: 19 October 2006

Abstract

Background

Our understanding of the mechanisms that govern the cellular process of meiosis is limited in higher plants with polyploid genomes. Bread wheat is an allohexaploid that behaves as a diploid during meiosis. Chromosome pairing is restricted to homologous chromosomes despite the presence of homoeologues in the nucleus. The importance of wheat as a crop and the extensive use of wild wheat relatives in breeding programs has prompted many years of cytogenetic and genetic research to develop an understanding of the control of chromosome pairing and recombination. The rapid advance of biochemical and molecular information on meiosis in model organisms such as yeast provides new opportunities to investigate the molecular basis of chromosome pairing control in wheat. However, building the link between the model and wheat requires points of data contact.

Results

We report here a large-scale transcriptomics study using the Affymetrix wheat GeneChip® aimed at providing this link between wheat and model systems and at identifying early meiotic genes. Analysis of the microarray data identified 1,350 transcripts temporally-regulated during the early stages of meiosis. Expression profiles with annotated transcript functions including chromatin condensation, synaptonemal complex formation, recombination and fertility were identified. From the 1,350 transcripts, 30 displayed at least an eight-fold expression change between and including pre-meiosis and telophase II, with more than 50% of these having no similarities to known sequences in NCBI and TIGR databases.

Conclusion

This resource is now available to support research into the molecular basis of pairing and recombination control in the complex polyploid, wheat.