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Lopez Arcondo, J. L.

Publications and source records attributed to Lopez Arcondo, J. L..

2 recordsLinked to original sources

Widespread synchronization of codon usage in functionally related genes

The usage of synonymous codons varies along the genome, with strong biases in conserved and highly expressed genes that are optimized for efficient translation. The extent to which selection shapes codon usage in other genes, as well as the associations between gene function, gene expression, and codon usage, remains an important open question. We developed and optimized a novel approach to detect synchronized changes in codon usage patterns and applied it to 15,005 species-representative bacterial genomes spanning the 15 most represented phyla. We show that codon usage is extensively shaped by selection in both highly and lowly expressed genes, with at least [~]20-46% of gene families showing synchronized codon usage evolution across genomes. We reveal that gene pairs with parallel codon usage adaptation are co-expressed, co-regulated, metabolically connected, and functionally associated. By identifying synchronized codon usage evolution between gene pairs, we have generated a genome-wide set of functional associations reflecting correlated expression across species. This underappreciated layer of coordinated codon usage adaptation has important implications for function discovery and engineering.

genomics↗

High-resolution quantification of the rhizosphere effect along a soil-to-root gradient shows selection-driven convergence of rhizosphere microbiomes

Plants secrete a complex array of organic compounds, constituting about a third of their photosynthetic products, into the surrounding soil. As a result, concentration gradients are established from the roots into the bulk soil, known as the rhizosphere. Soil microbes benefit from these root exudates for their survival and propagation, and consequently, the composition of the rhizosphere microbial community follows the gradient of available compounds, a phenomenon oftentimes referred to as the rhizosphere effect. However, the fine-grained changes in the microbial community along this soil-root gradient have not been well described. Yet such insights would enable us to underpin the ecological rules underlying root microbial community assembly. Therefore, here we harvested the roots of individual Arabidopsis thaliana plants grown in three different natural soils at high-resolution, such that we could interrogate community assembly and predict microbial growth rate across consecutive, fine-grained, rhizosphere compartments. We found that the strength of the rhizosphere effect depends on root proximity and that microbial communities closer to the roots harbour related microbes. Closer to the roots, microbial community assembly became less random and more driven by selection-based processes. Intriguingly, we observed priority effects, where related microbes that arrive first are more likely to establish, and that microbes might use different ecological growth strategies to colonise the rhizosphere. All effects appeared to be independent from starting conditions as microbial community composition converged on the root despite different soil microbial seed banks. Together, our results provide a high-resolution view of the microbiome changes across the soil-root gradient.

plant biology↗