SummaryAsy1, a protein required for meiotic chromosome synapsis, localizes to axis-associated chromatin in Arabidopsis and Brassica

Synapsis of homologous chromosomes is a key event in meiosis as it is essential for normal chromosome segregation and is implicated in the regulation of crossover frequency. We have previously reported the identification and cytological characterisation of a T-DNA-tagged asynaptic mutant of Arabidopsis thaliana. We have demonstrated that this mutant, asy1, is defective in meiosis in both males and females. Cloning and nucleotide sequencing of the ASY1 gene has revealed that it encodes a polypeptide of 596 amino acids that exhibits similarity to the HOP1 gene of Saccharomyces cerevisiae, which is known to encode a protein essential for synaptonemal complex assembly and normal synapsis. Expression studies indicate that, in common with a number of other Arabidopsis meiotic genes, ASY1 exhibits low-level expression in a range of plant tissues. Southern analysis coupled with database searching has resulted in the identification of an ASY1 homologue, ASY2. Although asy1 exhibits a strong asynaptic phenotype, a residual low level of synapsis indicates that ASY1 and ASY2 may exhibit a low degree of functional redundancy.

Meiosis is a key stage in the life cycle of all sexually reproducing eukaryotes. In plants, specialized reproductive cells differentiate from somatic tissue. These cells then undergo a single round of DNA replication followed by two rounds of chromosome division to produce haploid cells that then undergo further rounds of mitotic division to produce the pollen grain and embryo sac. A detailed cytological description of meiosis has been built up over many years, based on studies in a wide range of plants. Until recently, comparable molecular studies have proved too challenging, however, a number of groups are beginning to use Arabidopsis thaliana to overcome this problem. A range of meiotic mutants affecting key stages in meiosis have been identified using a combination of screening for plants exhibiting reduced fertility and, more recently, using a reverse genetics approach. These are now providing the means to identify and characterize the activity of key meiotic genes in flowering plants.

Arabidopsis has emerged as an important model for the analysis of meiosis in Angiosperm plants, creating an interesting and useful parallel to other model organisms. This development has been underpinned by advances in the molecular biology and genetics of Arabidopsis, especially the determination of its entire genome sequence. However, these advances alone would have been insufficient without the development of improved methods for cytological analysis and cytogenetic investigation of meiotic nuclei and chromosomes. A basic descriptive framework of meiosis in Arabidopsis has been established based on these procedures. In addition, molecular cytogenetic and immunocytological techniques have provided supplementary detailed information on some aspects of meiosis. Gene identification and characterization have proceeded in parallel with these developments based on both forward and reverse genetic procedures utilising the considerable range of Arabidopsis genetic and molecular resources, such as T-DNA and transposon tagged lines as well as the genomic DNA database, in combination with cytological analysis. A diverse range of meiotic genes have been identified and analysed by these procedures and in selected cases they have been subjected to detailed functional analysis. This review focuses on genes that are involved in the key meiotic events of chromosome synapsis and recombination.

We have identified a plant homologue of the Drosophila meiotic gene Pelota in Arabidopsis thaliana (AtPelota1). This gene maps to chromosome 4 of Arabidopsis and is one of two Pelota homologues present in this plant. When the expression pattern of AtPelota1 was examined it was found to be expressed at similar levels in all plant tissues tested (whole plant, bud, stem, leaf and root). This expression pattern corresponds to that seen for some other Arabidopsis meiotic genes and their homologues. A search of the databases reveal that the AtPelota gene family is widespread with homologues present in higher and lower eukaryotes and archaebacteria, but not eubacteria. Fig. 3 The expression of AtPelota1 was examined using RT-PCR. Reaction products were separated on a 1.2% agarose gel, blotted and probed with the full-length AtPelota1 cDNA. The predicted size for a product derived from mRNA was 368 bp, whereas a 563-bp product would indicate a genomic DNA origin. Samples were as follows: P, whole plant; B, bud; S, stem; L, leaf; R, root; and G, genomic DNA (control)