DArTseq-based analysis of genomic relationships among species of tribe Triticeae

Precise utilization of wild genetic resources to improve the resistance of their cultivated relatives to environmental growth limiting factors, such as salinity stress and diseases, requires a clear understanding of their genomic relationships. Although seriously criticized, analyzing these relationships in tribe Triticeae has largely been based on meiotic chromosome pairing in hybrids of wide crosses, a specialized and labourious strategy. In this study, DArTseq, an efficient genotyping-by-sequencing platform, was applied to analyze the genomes of 34 Triticeae species. We reconstructed the phylogenetic relationships among diploid and polyploid Aegilops and Triticum species, including hexaploid wheat. Tentatively, we have identified the diploid genomes that are likely to have been involved in the evolution of five polyploid species of Aegilops, which have remained unresolved for decades. Explanations which cast light on the progenitor of the A genomes and the complex genomic status of the B/G genomes of polyploid Triticum species in the Emmer and Timopheevi lineages of wheat have also been provided. This study has, therefore, demonstrated that DArTseq genotyping can be effectively applied to analyze the genomes of plants, especially where their genome sequence information are not available

Novel molecular marker-assisted strategy for production of wheat-Leymus mollis chromosome addition lines

Developing wheat–alien chromosome introgression lines to improve bread wheat’s resistance to stresses, such as drought, salinity stress and diseases, requires reliable markers to identify and characterize the alien chromatins. Leymus mollis is a wild relative of bread wheat resistant to salinity and economically important diseases of wheat, but its genome sequence and cytological markers are not available. We devised a molecular marker-assisted strategy for L. mollis chromosome identification and applied it to produce 10 wheat–L. mollis chromosome addition lines. Using 47 L. racemosus genome polymorphic PCR markers and DArTseq genotyping, we distinguished the L. mollis chromosomes and differentiated disomic and monosomic lines by progeny test. DArTseq genotyping generated 14,530 L. mollis SNP markers and the chromosome-specific SNP markers were used to determine the homoeologous groups of L. mollis chromosomes in the addition lines. To validate the marker-based results, genomic in situ hybridization was applied to confirm the presence and cytological status of L. mollis chromosomes in the lines. This study demonstrates that adequate molecular markers allow the production and characterization of wheat–alien addition lines without in situ hybridization, which saves considerable time and effort

DArTseq-based analysis of genomic relationships among species of tribe Triticeae

Precise utilization of wild genetic resources to improve the resistance of their cultivated relatives to environmental growth limiting factors, such as salinity stress and diseases, requires a clear understanding of their genomic relationships. Although seriously criticized, analyzing these relationships in tribe Triticeae has largely been based on meiotic chromosome pairing in hybrids of wide crosses, a specialized and labourious strategy. In this study, DArTseq, an efficient genotyping-by-sequencing platform, was applied to analyze the genomes of 34 Triticeae species. We reconstructed the phylogenetic relationships among diploid and polyploid Aegilops and Triticum species, including hexaploid wheat. Tentatively, we have identified the diploid genomes that are likely to have been involved in the evolution of five polyploid species of Aegilops, which have remained unresolved for decades. Explanations which cast light on the progenitor of the A genomes and the complex genomic status of the B/G genomes of polyploid Triticum species in the Emmer and Timopheevi lineages of wheat have also been provided. This study has, therefore, demonstrated that DArTseq genotyping can be effectively applied to analyze the genomes of plants, especially where their genome sequence information are not available

Metagenomics: an emerging tool for the chemistry of environmental remediation

Metagenomics is the study of genetic information, including the sequences and genomes of microorganisms present in an environment. Since 1998, the full-scale application of this technique to environmental chemistry has brought significant advances in the characterization of the nature and chemical composition/distribution of contaminants present in environmental matrices of contaminated and/or remediated sites. This has been critical in the selection of microorganisms and has contributed significantly to the success of this biological treatment over the years. Metagenomics has gone through different phases of development, which ranges from initial sequencing strategies to next-generation sequencing (NGS), which is a recently developed technology to obtain more robust deoxyribonucleic acid (DNA) profile of microorganisms devoid of chimeric sequences which reduces the quality of metagenomic data. Therefore, the objective of this review is to evaluate the applications of metagenomics in the understanding of environmental dynamics of chemical contaminants during remediation studies. Also, this review presents the relationship between biological characteristics of microorganisms and chemical properties of chemical compounds, which forms the basis of bioremediation and could be useful in developing predictive models that could enhance remediation efficiency. In conclusion, metagenomic techniques have improved the characterisation of chemical contaminants in the environment and provides a correlation for useful prediction of the type of contaminant expected in various environmental matrices