Cytogenetic Techniques for Analyzing Meiosis in Hexaploid Bread Wheat

Abstract

This chapter describes several cytogenetic procedures developed for investigating meiotic recombination in pollen mother cells (PMCs) of hexaploid wheat (Triticum aestivum) using standard fluorescence microscopy. Two basic methods are used to prepare slides for microscopy. In the cytological technique, wheat anthers are excised, fixed and used to prepare chromosome spreads which can be visualized following the application of a fluorescent DNA stain. In the immunocytological technique, fresh anthers are used to prepare chromosome spreads for analyzing the localization of meiotic proteins by applying specific antibodies followed by fluorescently tagged secondary antibodies. Both methods can be combined with the use of DNA probes to label specific chromosome regions such as telomeres, centromeres, and rDNA sequences in a procedure known as fluorescence in situ hybridisation (FISH). In addition, the cytological technique can be used in conjunction with S-phase incorporation of the DNA base analog, 5-bromo-2'-deoxyuridine (BrdU), and a modified immunolocalization procedure for a convenient meiotic time course assay. Although these protocols were developed for T. aestivum cv. Cadenza, they are directly applicable to other varieties and we have used them successfully for several other hexaploid cultivars and the tetraploid Triticum turgidum cv. Kronos.

Keywords: BrdU; Chromosomes; Cytology; FISH; Hexaploid; Immunolocalization; Meiosis; Recombination; Triticum aestivum; Wheat.