Transposable Element Junctions in Marker Development and Genomic Characterization of Barley

Barley is a model plant in genomic studies of Triticeae species. However, barley's large genome size and high repetitive sequence content complicate the whole‐genome sequencing. The majority of the barley genome is composed of transposable elements (TEs). In this study, TE repeat junctions (RJs) were used to develop a large‐scale molecular marker platform, as a prerequisite to genome assembly. A total of 10.22 Gb of barley nonassembled 454 sequencing data were screened with RJPrimers pipeline. In total, 9,881,561 TE junctions were identified. From detected RJs, 400,538 polymerase chain reaction (PCR)‐based RJ markers (RJMs) were designed across the genome, with an average of 39 markers/Mb. The utility of designed markers was tested using a random subset of RJMs. Over 94% of the markers successfully amplified amplicons, among which ∼90% were genome specific. In addition to marker design, identified RJs were utilized to detect 1190,885 TEs across the genome. In gene‐poor regions of the genome Gypsy elements comprised the majority of TEs (∼65%), while in gene‐rich regions Gypsy, Copia, and Mariner were the main transposons, each representing an average ∼23% of total TEs. The numerous RJ primer pairs developed in this study will be a valuable resource for barley genomic studies including genomic selection, fine mapping, and genome assembly. In addition, the results of this study show that characterizing RJs provides insight into TE composition of species without a sequenced genome but for which short‐read sequence data is available.

[1]  J. Dvorak,et al.  Physical mapping resources for large plant genomes: radiation hybrids for wheat D-genome progenitor Aegilops tauschii , 2012, BMC Genomics.

[2]  Mihaela M. Martis,et al.  A physical, genetic and functional sequence assembly of the barley genome. , 2022 .

[3]  Kazuhiro Sato,et al.  454 sequencing of pooled BAC clones on chromosome 3H of barley , 2011, BMC Genomics.

[4]  A. Flavell,et al.  Analysis of plant diversity with retrotransposon-based molecular markers , 2011, Heredity.

[5]  P. Capy,et al.  The struggle for life of the genome's selfish architects , 2011, Biology Direct.

[6]  Ming-Cheng Luo,et al.  RJPrimers: unique transposable element insertion junction discovery and PCR primer design for marker development , 2010, Nucleic Acids Res..

[7]  Hsueh-Sheng Wu,et al.  What Are Categorical Data ? , 2010 .

[8]  M. Metzker Sequencing technologies — the next generation , 2010, Nature Reviews Genetics.

[9]  M. Platzer,et al.  A whole-genome snapshot of 454 sequences exposes the composition of the barley genome and provides evidence for parallel evolution of genome size in wheat and barley. , 2009, The Plant journal : for cell and molecular biology.

[10]  D. Coleman-Derr,et al.  Rapid development of PCR-based genome-specific repetitive DNA junction markers in wheat. , 2009, Genome.

[11]  P. Langridge,et al.  Genetic Mapping in the Triticeae , 2009 .

[12]  Pierre Sourdille,et al.  A Physical Map of the 1-Gigabase Bread Wheat Chromosome 3B , 2008, Science.

[13]  Christopher D Town,et al.  A first survey of the rye (Secale cereale) genome composition through BAC end sequencing of the short arm of chromosome 1R , 2008, BMC Plant Biology.

[14]  S. Ullrich,et al.  Barley for food: Characteristics, improvement, and renewed interest , 2008 .

[15]  Paul A. Watters,et al.  Statistics in a nutshell - a desktop quick reference , 2008 .

[16]  Pascal Condamine,et al.  Coupling amplified DNA from flow-sorted chromosomes to high-density SNP mapping in barley , 2008, BMC Genomics.

[17]  J. Bennetzen,et al.  A unified classification system for eukaryotic transposable elements , 2007, Nature Reviews Genetics.

[18]  C. Feuillet,et al.  Characterizing the composition and evolution of homoeologous genomes in hexaploid wheat through BAC-end sequencing on chromosome 3B. , 2006, The Plant journal : for cell and molecular biology.

[19]  Agnes P Chan,et al.  Uneven chromosome contraction and expansion in the maize genome. , 2006, Genome research.

[20]  J. Doležel,et al.  Dissection of the nuclear genome of barley by chromosome flow sorting , 2006, Theoretical and Applied Genetics.

[21]  Jianxin Ma,et al.  Analysis and mapping of randomly chosen bacterial artificial chromosome clones from hexaploid bread wheat. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[22]  Richard M. Clark,et al.  Estimating a nucleotide substitution rate for maize from polymorphism at a major domestication locus. , 2005, Molecular biology and evolution.

[23]  S. Nasuda,et al.  Chromosomal assignment and deletion mapping of barley EST markers. , 2005, Genes & genetic systems.

[24]  W. McCombie,et al.  Differential methylation of genes and repeats in land plants. , 2005, Genome research.

[25]  B. Gill,et al.  Sequence composition, organization, and evolution of the core Triticeae genome. , 2004, The Plant journal : for cell and molecular biology.

[26]  Yong Qiang Gu,et al.  Rapid Genome Evolution Revealed by Comparative Sequence Analysis of Orthologous Regions from Four Triticeae Genomes , 2004, Plant Physiology.

[27]  D. Sandhu,et al.  Demarcating the gene-rich regions of the wheat genome. , 2004, Nucleic acids research.

[28]  J. Bennetzen,et al.  Transposable element contributions to plant gene and genome evolution , 2004, Plant Molecular Biology.

[29]  Cédric Feschotte,et al.  Plant transposable elements: where genetics meets genomics , 2002, Nature Reviews Genetics.

[30]  J. Bennetzen,et al.  Transposable elements, genes and recombination in a 215-kb contig from wheat chromosome 5Am , 2002, Functional & Integrative Genomics.

[31]  T. Wicker,et al.  Analysis of a contiguous 211 kb sequence in diploid wheat (Triticum monococcum L.) reveals multiple mechanisms of genome evolution. , 2001, The Plant journal : for cell and molecular biology.

[32]  A. Meister,et al.  Cytologically integrated physical restriction fragment length polymorphism maps for the barley genome based on translocation breakpoints. , 2000, Genetics.

[33]  S. Wessler,et al.  Mobile inverted-repeat elements of the Tourist family are associated with the genes of many cereal grasses. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[34]  P. Langridge,et al.  Cloning and characterisation of a new rye-specific repeated sequence , 1991 .