High-Resolution Comparative Analysis between Barley and B. distachyon.
High-density comparative analysis of the linear gene order of the barley genome zippers versus the sequenced model grass genome of Brachypodium. The figure includes four sets of concentric circles: the inner circle represents the seven chromosomes of barley scaled according to the barley genetic map (bars at 10-cM intervals). Each barley chromosome is assigned a color according to the sequence on the color key, starting with chr1 through chr7. The positions of the barley centromeres are indicated by black bars. Moving outwards, the second circle illustrates a schematic model of the seven barley chromosomes, but this time color-coded according to blocks of conserved synteny with the model genome. The color coding is again based on the sequence on the color key, but this time is based on the model genome linkage groups, starting with chr1 through chr5 for Brachypodium. Boxes extending from these colored bars indicate regions involved in larger-scale structural changes (e.g., inversions). The outer partially complete circles of heat map colored bars represent pseudomolecules of the model genome linkage groups arranged according to conserved synteny with barley 1H-7H. When pairs of adjacent heat map bars are shown, they illustrate where the homologs of a short (inner heat map bar) or a long (outer heat map bar) barley chromosome arm data set is allocated to the respective model genome pseudochromosome. The heat maps illustrate the density of genes hit by the 454 shotgun reads from the relevant barley chromosome arm. Conserved syntenic regions are highlighted by yellow-red–colored regions. Putative orthologs between barley and the model genomes are connected with lines (colored according to model genome chromosomes) between the second and third circles. Colored lines in the center represent putative paralogous relationships between barley chromosomes on the basis of fl-cDNA supported genes included in the genome zipper models of the seven barley chromosomes.

High-Resolution Comparative Analysis between Barley and Rice.
High-density comparative analysis of the linear gene order of the barley genome zippers versus the sequenced model grass genome of rice. Details are as provided in the Figure 1 legend. Putative orthologs between barley and the rice genomes are connected with lines (colored according to model genome chromosomes) between second, third, and fourth circles. In the center, nine major segmental duplications of the barley genome are visualized as statistically significant groups of paralogous genes. Each line represents a duplicated gene (paralogous gene pair). Black lines indicate ancestral duplications shared with the model grass genomes, and gray lines highlight barley-specific duplications.

Barley-Centered Four-Genome Comparative View of Grass Genome Collinearity.
The seven barley chromosomes (Hv1 to Hv7) are depicted by the inner circle of colored bars exactly as in Figure 1. The heat map attached to each chromosome indicates the density of barley fl-cDNAs anchored and positioned along the chromosomes according to the genome zipper models. Gene density is colored according to the heat map scale. Moving outwards, the bars represent a schematic diagram of the barley chromosomes colored according to conserved synteny with the genomes of Brachypodium (Bd), rice (Os), and sorghum (Sb), respectively. In each case, the chromosome numbers and segments are colored according to the chromosome color code (i.e., chr1 through chr5 for Bd, chr1 through chr12 for Os, and chr1 through chr10 for Sb). As in Figure 1, boxes extending from the colored bars indicate structural changes (e.g., inversions) between the gene order in barley and the respective model genome. To the outside of each model genome chromosome, box graphs show the z-score derived from a sliding window analysis of the frequency of fl-cDNAs present at a conserved syntenic position with their corresponding orthologs in Bd, Os, and Sb, respectively (see Methods for a full description of the analysis). A z-score >0 indicates higher than the average conservation of synteny, and a z-score <0 highlights decreased syntenic conservation. The data points in the center of the diagram depict the K_a/K_s ratios between barley full-length genes and their orthologs in Bd, Os, and Sb. Values against Bd are plotted as dark red rectangles, against Os in red circles, and against Sb in blue triangles.

Structure of Wheat Chromosome 4A in Relation to the Barley Genome Zipper.
Wheat subgenome specific markers of chromosome 4A have been compared against the genome zipper chromosome model of barley (for a genome-wide overview, see Supplemental Figure 5 online). Orthologous regions are depicted and visualized by a heatmap.
(A) Wheat EST markers allocated to 4AS cross-match to barley genes on 4HL and markers allocated to 4AS, a small region on 4AL, 5AL, and 7BS cross-match to 4HL. Thus, a reciprocal translocation involving chromosomes 4A and 5A and a translocation from 7BS to 4AL was detected. Compared with barley 4H, wheat chromosome 4A contains a pericentromeric inversion.
(B) The barley genome zipper model allows the size of the affected regions to be estimated and the minimal number of genes located in these rearranged regions of the wheat chromosomes to be predicted.