Orientation of Fitch Graphs and Reconciliation-Free Inference of Horizontal Gene Transfer in Gene Trees

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Publication:6072286

DOI10.1137/22M150736XarXiv2112.00403OpenAlexW4387060342MaRDI QIDQ6072286FDOQ6072286


Authors: David Schaller, Marc Hellmuth, Peter F. Stadler Edit this on Wikidata


Publication date: 13 October 2023

Published in: SIAM Journal on Discrete Mathematics (Search for Journal in Brave)

Abstract: Horizontal gene transfer events partition a gene tree T and thus, its leaf set into subsets of genes whose evolutionary history is described by speciation and duplication events alone. Indirect phylogenetic methods can be used to infer such partitions mathcalP from sequence similarity or evolutionary distances without any a priory knowledge about the underlying tree T. In this contribution, we assume that such a partition mathcalP of a set of genes X is given and that, independently, an estimate T of the original gene tree on X has been derived. We then ask to what extent T and the xenology information, i.e., mathcalP can be combined to determine the horizontal transfer edges in T. We show that for each pair of genes x and y with x,y being in different parts of mathcalP, it can be decided whether there always exists or never exists a horizontal gene transfer in T along the path connecting y and the most recent common ancestor of x and y. This problem is equivalent to determining the presence or absence of the directed edge (x,y) in so-called Fitch graphs; a more fine-grained version of graphs that represent the dependencies between the sets in mathcalP. We then consider the generalization to insufficiently resolved gene trees and show that analogous results can be obtained. We show that the classification of (x,y) can be computed in constant time after linear-time preprocessing. Using simulated gene family histories, we observe empirically that the vast majority of horizontal transfer edges in the gene tree T can be recovered unambiguously.


Full work available at URL: https://arxiv.org/abs/2112.00403







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