It is shown that this context - the grammar of gene content - provides a rich source of information that can be used to greatly improve ancestral gene content inference and metabolic reconstruction under both the reconciliation-and profile-based approaches.
Abstract
Ancestral gene content inferences allow inferring the set of genes - and by extension, the cellular features and metabolic capabilities - of ancestral organisms, based on data from modern genomes. Current methods differ in their approach to ancestral inferences and the kinds of errors they make: reconciliation methods map gene trees onto species trees, and tend to underestimate ancestral contents due to phylogenetic noise; profile methods model the evolution of phylogenetic profiles (presence-absence or count data) on the species tree, and tend to return inflated ancestors because they ignore gene trees and as a result can only account for horizontal gene transfer (HGT) in a limited manner. For reasons of tractability, both approaches also share a core limitation: neither uses the fact that genes do not act alone but belong to operons, protein complexes, and metabolic pathways that may be gained and lost together or experience shared selective constraints. Here, we show that this context - the grammar of gene content - provides a rich source of information that can be used to greatly improve ancestral gene content inference and metabolic reconstruction under both the reconciliation-and profile-based approaches. We model this structure as an Ising model and infer its parameters from 113,104 bacterial and archaeal genomes (one per species representative in GTDB). We validate the model on extant taxa using phylum-level holdout (i.e. using test data from different prokaryotic phyla than training data), showing that it can accurately “denoise”, i.e., reconstruct gene repertoires from highly fragmented and noisy input data, learning about protein-protein interactions and gene essentiality during the training process. When applied to ancestral reconstructions, the denoiser fills gaps in conservative reconstructions and removes excess genes from overly-generous ones, such that different reconstruction methods converge to broadly concordant conclusions. By using this gene content grammar, patchy method-dependent ancestral reconstructions can be turned into organism-like ones, and yield agreement on the gene families, cell-biological features, and metabolic capabilities of the deepest nodes in the tree of life.
Chromosome-scale conservation of gene linkage (‘macrosynteny’) provides phylogenetic characters largely independent of sequence data. Fusion of ancestral linkage groups, and especially the subsequent interspersion (“mixing”) of their genes, is argued to be effectively irreversible, and such synapomorphic events have be...
Abstract Bacterial genomes are dynamic, shaped by gene gain, loss, and horizontal transfer; yet selection preserves the colocalization of functionally coupled genes into recurrent modules known as syntons. Many large-scale approaches do not explicitly account for phylogenetic relatedness between genomes which can infla...
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Gene duplication promotes the generation of novel gene functions and trait diversity across species. Here, we present DupHIST, a computational pipeline that reconstructs the hierarchical timing of gene duplications by integrating maximum likelihood (ML)-based phylogeny with substitution-derived timing via statistical s...
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Large phylogenetic trees are often unbalanced near the root, with a species-depauperate lineage sister to a far more species-rich clade. The species-poor branches, sometimes referred to as "early diverging," are often viewed as key sources of information about deep evolutionary history. As a result, these lineages occu...
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