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Garcia-Dominguez, R.

Publications and source records attributed to Garcia-Dominguez, R..

2 recordsLinked to original sources

Domain-combination based pan-genomic Tree of Life

Reconstructing the Tree of Life (ToL) remains a central challenge in evolutionary biology. While sequence-based methods have resolved much of lifes diversity, deep evolutionary relationships often remain elusive, particularly across the three superkingdoms of life. Here, we present a complementary approach using genome-wide occurrence of protein domain combinations as phylogenetic signal. We analyzed 5,343 complete proteomes spanning Bacteria, Archaea, and Eukaryota, and inferred a pan-genomic ToL from [~]77,000 domain combinations, including isolated domains and domain pairs. Our reconstruction recovers major clades and captures both vertical inheritance and signals from non-vertical processes such as lateral gene transfer, endosymbiosis, and genome reduction. Ancestral reconstructions reveal functional innovations that mark key evolutionary transitions--such as the emergence of vesicle trafficking in Eukaryota or methanogenesis in Archaea. We found that organisms with reduced genomes, like Chlamydiota, tend to be misplaced in domain combination-based phylogenies due to sparse combinatorial data. Our results demonstrate that domain combinations carry a strong, evolutionary signal that is both biologically and functionally informative. While not a substitute for sequence-based phylogenetics, domain combination-based trees offer an alternative perspective, capable of integrating both vertical and lateral processes into a unified evolutionary framework. Author SummaryTraditional evolutionary trees are typically built from sequences, but this approach struggles to resolve deep branches in the Tree of Life. Here, we use combinations of protein domains--the functional modules that make up proteins to resolve major relationships in the tree. By analyzing over 5,000 complete proteomes from Bacteria, Archaea, and Eukaryotes, we reconstruct a Tree of Life that reflects both vertical inheritance and key evolutionary processes like endosymbiosis and gene transfer. This domain-based approach not only recovers known relationships but also reveals how major biological innovations emerged. Our results show that domain combinations provide a powerful and interpretable signal for studying evolution at a genomic scale.

evolutionary biology↗

Unraveling the pathway of Copper Delivery to Cytochrome c oxidases in the Free-Living Bacterium Caulobacter vibrioides

Copper (Cu) is an essential micronutrient that serves as a cofactor for many enzymes but becomes toxic when present in excess. In most bacteria, CopA-like P1B-type ATPases mediate Cu detoxification by exporting cytoplasmic Cu to the periplasm or extracellular environment. In this study, we show that Caulobacter vibrioides lacks a canonical CopA-like ATPase but encodes a single FixI/CcoI-type Cu-transporting ATPase, previously implicated in Cu delivery to the cbb{square}-type cytochrome c oxidase (Cox) in species such as Rhodobacter capsulatus. C. vibrioides harbors two terminal cytochrome c oxidases in its cytoplasmic membrane: an aa{square}-type and a cbb{square}-type Cox. We also demonstrate that the activity of cbb{square}-Cox requires the FixI-type Cu transporter and the periplasmic Cu chaperone PccA. In contrast, aa{square}-Cox activity depends on PccA and the inner membrane-bound protein CtaG. Since the mechanism of Cu acquisition for aa{square}-Cox remains largely unknown, we conducted a genetic screen and identified a novel outer membrane TonB-dependent receptor (TccA) that is specifically required for aa{square}-Cox function. We also showed that cbb{square}-Cox is upregulated under microaerobic conditions, possibly such as those encountered on solid media where O2 diffusion is limited. Under normoxic conditions, the expression and the activity of cbb{square}-Cox decrease, and aa{square}-Cox becomes the predominant terminal oxidase. These findings demonstrate that C. vibrioides differentially utilizes its Cox enzymes in response to O2 availability and relies on a distinct Cu trafficking pathway for their maturation, including an outer membrane component that has not been previously described in bacterial Cu homeostasis.

microbiology↗