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Ramirez, C. J.

Publications and source records attributed to Ramirez, C. J..

2 recordsLinked to original sources

A pangenome-graph approach for mapping and imputing barley sequences

Barley (Hordeum vulgare) is a key cereal crop with exceptional adaptation to diverse environments. With a large, highly repetitive diploid genome, barley presents challenges for pangenome representation. Starting from the reference genome MorexV3, we describe the construction of a barley graph (Pan20) representing the global diversity of landraces and cultivars captured in the public pangenome V1. For mapping arbitrary sequences, a greedy strategy is proposed that combines GMAP alignment followed by intersection with a Practical Haplotype Graph (PHG). This enables presence-absence variation detection and provides a consistent MorexV3 physical coordinate system across genotypes, enabling comparative analysis and visualization. For imputation of genomic data, the PHG approach relies on k-mer pseudo-alignment against the graph. Benchmarks show that Pan20 can accurately align barley genomic and transcriptomic sequences, including those not present in the Morex reference, revealing that a third of long genomic sequences map on non-reference genomes. Moreover, experiments with Genotyping by Sequencing and low-pass sequencing data indicate that FASTQ files can be efficiently mapped and imputed against the graph, preserving local haplotype context. This flexible and scalable graph framework allows barley researchers to explore genetic diversity beyond a single reference and facilitates analysis of diversity panels at the haplotype level, going beyond SNPs. Documentation and a Docker container are available at https://github.com/eead-csic-compbio/barleygraph. The graph sequence mapping utility was added to the Web application https://barleymap.eead.csic.es.

genomics↗

Complex organic matter degradation by secondary consumers in chemolithoautotrophy-based subsurface geothermal ecosystems

Microbial communities in terrestrial geothermal systems often contain chemolithoautotrophs with well-characterized distributions and metabolic capabilities. However, the extent to which organic matter produced by these chemolithoautotrophs supports heterotrophs remains largely unknown. Here we compared the abundance and activity of peptidases and carbohydrate active enzymes (CAZymes) that are predicted to be extracellular identified in metagenomic assemblies from 63 springs in the Central American and the Andean convergent margin (Argentinian backarc of the Central Volcanic Zone), as well as the plume-influenced spreading center in Iceland. All assemblies contain two orders of magnitude more peptidases than CAZymes, suggesting that the microorganisms more often use proteins for their carbon and/or nitrogen acquisition instead of complex sugars. The CAZy families in highest abundance are GH23 and CBM50, and the most abundant peptidase families are M23 and C26, all four of which degrade peptidoglycan found in bacterial cells. This implies that the heterotrophic community relies on autochthonous dead cell biomass, rather than allochthonous plant matter, for organic material. Enzymes involved in the degradation of cyanobacterial- and algal-derived compounds are in lower abundance at every site, with volcanic sites having more enzymes degrading cyanobacterial compounds and non-volcanic sites having more enzymes degrading algal compounds. Activity assays showed that many of these enzyme classes are active in these samples. High temperature sites (> 80{degrees}C) had similar extracellular carbon-degrading enzymes regardless of their province, suggesting a less well-developed population of secondary consumers at these sites, possibly connected with the limited extent of the subsurface biosphere in these high temperature sites. We conclude that in < 80{degrees}C springs, chemolithoautotrophic production supports heterotrophs capable of degrading a wide range of organic compounds that do not vary by geological province, even though the taxonomic and respiratory repertoire of chemolithoautotrophs and heterotrophs differ greatly across these regions.

biochemistry↗