Cited by 77Genomics and Phylogenetic StudiesGenome Rearrangement AlgorithmsChromosomal and Genetic Variations

Most parsimonious reconciliation in the presence of gene duplication, loss, and deep coalescence using labeled coalescent trees

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Wu, Yi-Chieh, Rasmussen, Matthew D., Bansal, Mukul S., Kellis, Manolis·2014·Genome Research

Abstract

Accurate gene tree-species tree reconciliation is fundamental to inferring the evolutionary history of a gene family. However, although it has long been appreciated that population-related effects such as incomplete lineage sorting (ILS) can dramatically affect the gene tree, many of the most popular reconciliation methods consider discordance only due to gene duplication and loss (and sometimes horizontal gene transfer). Methods that do model ILS are either highly parameterized or consider a restricted set of histories, thus limiting their applicability and accuracy. To address these challenges, we present a novel algorithm DLCpar for inferring a most parsimonious (MP) history of a gene family in the presence of duplications, losses, and ILS. Our algorithm relies on a new reconciliation structure, the labeled coalescent tree (LCT), that simultaneously describes coalescent and duplication-loss history. We show that the LCT representation enables an exhaustive and efficient search over the space of reconciliations, and, for most gene families, the least common ancestor (LCA) mapping is an optimal solution for the species mapping between the gene tree and species tree in an MP LCT. Applying our algorithm to a variety of clades, including flies, fungi, and primates, as well as to simulated phylogenies, we achieve high accuracy, comparable to sophisticated probabilistic reconciliation methods, at reduced run time and with far fewer parameters. These properties enable inferences of the complex evolution of gene families across a broad range of species and large data sets.

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  • DLCpar (search) employs an iterative search for a locally optimal solution, which can differ from the globally optimal solution.

    “DLCpar (search) instead employs an iterative search for a locally optimal solution, which can differ from the globally optimal solution.”

    From OrthoFinder: phylogenetic orthology inference for comparative genomics (2019) · cites this paper as [32]

    The Methods section describes DLCpar as searching over all possible most-parsimonious reconciliations, and the Discussion says it explores the reconciliation space exhaustively. The paper instead attributes a hill-climbing, heuristic search to DLCoalRecon. It does not describe DLCpar as an iterative search that may stop at a local optimum. (LLM, conf=0.89)

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    Experimental — accuracy not yet measured
  • DLCpar (full) can have large runtimes even for relatively small gene trees.

    “DLCpar (full) considers the complete space of possible reconciliations to find the maximum parsimony solution under the DLC model but can have large runtimes even for relatively small gene trees.”

    From OrthoFinder: phylogenetic orthology inference for comparative genomics (2019) · cites this paper as [32]

    The Results (Biological data set of 16 fungal genomes; page unavailable) report that DLCpar runtimes can be long, but say the average is highly skewed by large gene families. The paper supports exhaustive reconciliation search; it does not establish the claim that runtimes can be large even for relatively small gene trees. (LLM, conf=0.85)

    Experimental — accuracy not yet measured
  • The novel OrthoFinder method outperformed all methods other than DLCpar (full) in terms of accuracy on two independent simulated datasets.

    “In terms of accuracy, the novel OrthoFinder method outperformed all methods other than DLCpar (full) (Fig. 5a, Additional file 1: Table S2).”

    From OrthoFinder: phylogenetic orthology inference for comparative genomics (2019) · cites this paper as [32]

    The Results section on simulated data sets compares DLCpar with DLCoalRecon and MPR on fly and primate data sets. Searches for OrthoFinder and “DLCpar (full)” found no passage evaluating OrthoFinder, so this copy cannot verify the attributed accuracy ranking. (LLM, conf=0.76)

    Experimental — accuracy not yet measured

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Cited by

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Authors
Wu, Y.-C., Rasmussen, M. D., Bansal, M. S., & Kellis, M.
Affiliations
  • MIT Computer Science and Artificial Intelligence Laboratory (US)
  • Cornell University (US)
  • Broad Institute (US)
Corresponding author
  • Wu, Yi-Chieh
  • Kellis, Manolis
Venue
Genome Research
Published
2013-12-05
Volume
24
Issue
3
Pages
475-486
ISSN
1088-9051 (ISSN-L)
OpenAlex
W2120836981
Cited by
77
References
1
Citations by year
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Type
posted content
Language
en
Open access
Locations
  • Genome Research (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
  • HighWire Press Open Archive (submittedVersion)
Funders
  • National Science Foundation (0644282, CAREER)
  • National Institutes of Health
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genome Rearrangement Algorithms
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
Keywords
gene tree-species tree reconciliation, gene duplication, gene loss, incomplete lineage sorting, gene family evolution
MeSH terms
Algorithms, Animals, Diptera, Fungi, Genes, Multigene Family, Models, Genetic, Phylogeny, Primates, Species Specificity, Genome, Gene Deletion, Evolution, Molecular, Gene Duplication, Gene Transfer, Horizontal

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