» Articles » PMID: 11999849

A High-density Cytogenetic Map of the Aegilops Tauschii Genome Incorporating Retrotransposons and Defense-related Genes: Insights into Cereal Chromosome Structure and Function

Overview
Journal Plant Mol Biol
Date 2002 May 10
PMID 11999849
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Aegilops tauschii (Coss.) Schmal. (2n = 2x = 14, DD) (syn. A. squarrosa L.; Triticum tauschii) is well known as the D-genome donor of bread wheat (T. aestivum, 2n = 6x = 42, AABBDD). Because of conserved synteny, a high-density map of the A. tauschii genome will be useful for breeding and genetics within the tribe Triticeae which besides bread wheat also includes barley and rye. We have placed 249 new loci onto a high-density integrated cytological and genetic map of A. tauschii for a total of 732 loci making it one of the most extensive maps produced to date for the Triticeae species. Of the mapped loci, 160 are defense-related genes. The retrotransposon marker system recently developed for cultivated barley (Hordeum vulgare L.) was successfully applied to A. tauschii with the placement of 80 retrotransposon loci onto the map. A total of 50 microsatellite and ISSR loci were also added. Most of the retrotransposon loci, resistance (R), and defense-response (DR) genes are organized into clusters: retrotransposon clusters in the pericentromeric regions, R and DR gene clusters in distal/telomeric regions. Markers are non-randomly distributed with low density in the pericentromeric regions and marker clusters in the distal regions. A significant correlation between the physical density of markers (number of markers mapped to the chromosome segment/physical length of the same segment in microm) and recombination rate (genetic length of a chromosome segment/physical length of the same segment in microm) was demonstrated. Discrete regions of negative or positive interference (an excess or deficiency of crossovers in adjacent intervals relative to the expected rates on the assumption of no interference) was observed in most of the chromosomes. Surprisingly, pericentromeric regions showed negative interference. Islands with negative, positive and/or no interference were present in interstitial and distal regions. Most of the positive interference was restricted to the long arms. The model of chromosome structure and function in cereals with large genomes that emerges from these studies is discussed.

Citing Articles

MIG-seq is an effective method for high-throughput genotyping in wheat (Triticum spp.).

Nishimura K, Motoki K, Yamazaki A, Takisawa R, Yasui Y, Kawai T DNA Res. 2022; 29(2).

PMID: 35412600 PMC: 9035812. DOI: 10.1093/dnares/dsac011.


High-throughput retrotransposon-based genetic diversity of maize germplasm assessment and analysis.

Ghonaim M, Kalendar R, Barakat H, Elsherif N, Ashry N, Schulman A Mol Biol Rep. 2020; 47(3):1589-1603.

PMID: 31919750 DOI: 10.1007/s11033-020-05246-4.


An Update of Recent Use of Species in Wheat Breeding.

Kishii M Front Plant Sci. 2019; 10:585.

PMID: 31143197 PMC: 6521781. DOI: 10.3389/fpls.2019.00585.


Molecular mapping of resistance gene to English grain aphid (Sitobion avenae F.) in Triticum durum wheat line C273.

Liu X, Yang X, Wang C, Wang Y, Zhang H, Ji W Theor Appl Genet. 2011; 124(2):287-93.

PMID: 21953208 DOI: 10.1007/s00122-011-1704-7.


Microsatellite mapping of Ae. speltoides and map-based comparative analysis of the S, G, and B genomes of Triticeae species.

Dobrovolskaya O, Boeuf C, Salse J, Pont C, Sourdille P, Bernard M Theor Appl Genet. 2011; 123(7):1145-57.

PMID: 21792632 DOI: 10.1007/s00122-011-1655-z.


References
1.
Noel L, Moores T, van der Biezen E, Parniske M, Daniels M, Parker J . Pronounced intraspecific haplotype divergence at the RPP5 complex disease resistance locus of Arabidopsis. Plant Cell. 1999; 11(11):2099-112. PMC: 144120. View

2.
Wicker T, Stein N, Albar L, Feuillet C, Schlagenhauf E, Keller B . Analysis of a contiguous 211 kb sequence in diploid wheat (Triticum monococcum L.) reveals multiple mechanisms of genome evolution. Plant J. 2001; 26(3):307-16. DOI: 10.1046/j.1365-313x.2001.01028.x. View

3.
Pearce S, Harrison G, Flavell A, Kumar A . Characterization and genomic organization of Ty1-copia group retrotransposons in rye (Secale cereale). Genome. 1997; 40(5):617-25. DOI: 10.1139/g97-081. View

4.
Gribbon B, Pearce S, Kalendar R, Schulman A, Paulin L, Jack P . Phylogeny and transpositional activity of Ty1-copia group retrotransposons in cereal genomes. Mol Gen Genet. 1999; 261(6):883-91. DOI: 10.1007/pl00008635. View

5.
Gill K, Gill B, Endo T, Taylor T . Identification and high-density mapping of gene-rich regions in chromosome group 1 of wheat. Genetics. 1996; 144(4):1883-91. PMC: 1207735. DOI: 10.1093/genetics/144.4.1883. View