Synteny perturbations between wheat homoeologous chromosomes caused by locus duplications and deletions correlate with recombination rates. 2003

Eduard D Akhunov, and Alina R Akhunova, and Anna M Linkiewicz, and Jorge Dubcovsky, and David Hummel, and Gerry Lazo, and Shiaoman Chao, and Olin D Anderson, and Jacques David, and Lili Qi, and Benjamin Echalier, and Bikram S Gill, and Miftahudin, and J Perry Gustafson, and Mauricio La Rota, and Mark E Sorrells, and Deshui Zhang, and Henry T Nguyen, and Venugopal Kalavacharla, and Khwaja Hossain, and Shahryar F Kianian, and Junhua Peng, and Nora L V Lapitan, and Emily J Wennerlind, and Vivienne Nduati, and James A Anderson, and Deepak Sidhu, and Kulvinder S Gill, and Patrick E McGuire, and Calvin O Qualset, and Jan Dvorak
Department of Agronomy and Range Science, University of California, Davis, CA 95616, USA.

Loci detected by Southern blot hybridization of 3,977 expressed sequence tag unigenes were mapped into 159 chromosome bins delineated by breakpoints of a series of overlapping deletions. These data were used to assess synteny levels along homoeologous chromosomes of the wheat A, B, and D genomes, in relation to both bin position on the centromere-telomere axis and the gradient of recombination rates along chromosome arms. Synteny level decreased with the distance of a chromosome region from the centromere. It also decreased with an increase in recombination rates along the average chromosome arm. There were twice as many unique loci in the B genome than in the A and D genomes, and synteny levels between the B genome chromosomes and the A and D genome homoeologues were lower than those between the A and D genome homoeologues. These differences among the wheat genomes were attributed to differences in the mating systems of wheat diploid ancestors. Synteny perturbations were characterized in 31 paralogous sets of loci with perturbed synteny. Both insertions and deletions of loci were detected and both preferentially occurred in high recombination regions of chromosomes.

UI MeSH Term Description Entries
D011995 Recombination, Genetic Production of new arrangements of DNA by various mechanisms such as assortment and segregation, CROSSING OVER; GENE CONVERSION; GENETIC TRANSFORMATION; GENETIC CONJUGATION; GENETIC TRANSDUCTION; or mixed infection of viruses. Genetic Recombination,Recombination,Genetic Recombinations,Recombinations,Recombinations, Genetic
D014908 Triticum A plant genus of the family POACEAE that is the source of EDIBLE GRAIN. A hybrid with rye (SECALE CEREALE) is called TRITICALE. The seed is ground into FLOUR and used to make BREAD, and is the source of WHEAT GERM AGGLUTININS. Wheat,Durum Wheat,Triticum aestivum,Triticum durum,Triticum spelta,Triticum turgidum,Triticum turgidum subsp. durum,Triticum vulgare,Durum Wheats,Wheat, Durum
D017353 Gene Deletion A genetic rearrangement through loss of segments of DNA or RNA, bringing sequences which are normally separated into close proximity. This deletion may be detected using cytogenetic techniques and can also be inferred from the phenotype, indicating a deletion at one specific locus. Deletion, Gene,Deletions, Gene,Gene Deletions
D020440 Gene Duplication Processes occurring in various organisms by which new genes are copied. Gene duplication may result in a MULTIGENE FAMILY; supergenes or PSEUDOGENES. Duplication, Gene,Duplications, Gene,Gene Duplications
D032461 Chromosomes, Plant Complex nucleoprotein structures which contain the genomic DNA and are part of the CELL NUCLEUS of PLANTS. Chromosome, Plant,Plant Chromosome,Plant Chromosomes

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