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Related Concept Videos

Phylogenetic Trees03:21

Phylogenetic Trees

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Phylogenetic trees come in many forms. It matters in which sequence the organisms are arranged from the bottom to the top of the tree, but the branches can rotate at their nodes without altering the information. The lines connecting individual nodes can be straight, angled, or even curved.
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Evolutionary Relationships through Genome Comparisons02:54

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Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Phylogeny is concerned with the evolutionary diversification of organisms or groups of organisms. A group of organisms with a name is called a taxon (singular). Taxa (plural) can span different levels of the evolutionary hierarchy. For instance, the group containing all birds is a taxon (comprising the class Aves), and the group of all species of daisies (the genus Bellis) is a taxon. Phylogenies can likewise include just one genus (i.e., depict species relationships) or span an entire kingdom.
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The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
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Types of Genetic Transfer Between Organisms02:18

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Genetic transfer occurs when genetic information is passed from one organism to another. It occurs via two mechanisms: vertical gene transfer and horizontal gene transfer. Vertical gene transfer occurs when genetic information is transferred from one generation to the next, which happens much more frequently than horizontal gene transfer. Both sexual and asexual reproduction are forms of vertical gene transfer, where one or more organisms pass some or all of their genome onto their progeny.
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Gene Duplication and Divergence02:37

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The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was  generated by gene duplication and divergence, indicating its critical role in evolution.
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Using Phylogenetic Analysis to Investigate Eukaryotic Gene Origin
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Embedding gene trees into phylogenetic networks by conflict resolution algorithms.

Marcin Wawerka1, Dawid Dąbkowski2, Natalia Rutecka2

  • 1University of Warsaw, Faculty of Mathematics, Informatics and Mechanics, Banacha 2, 02-097, Warsaw, Poland. marcin.wawerka@gmail.com.

Algorithms for Molecular Biology : AMB
|May 19, 2022
PubMed
Summary

This study introduces efficient algorithms for inferring optimal displayed trees from phylogenetic networks, crucial for understanding evolutionary histories shaped by reticulate events like hybridization.

Keywords:
Deep coalescenceGene treeOptimal displayed treePhylogenetic networkReticulationSpecies treeTree-child network

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Area of Science:

  • Evolutionary biology
  • Computational phylogenetics
  • Bioinformatics

Background:

  • Phylogenetic networks model evolutionary processes with reticulate events (hybridization, recombination, HGT).
  • Displayed trees are derived from networks by removing reticulation edges.
  • Displayed trees can represent gene family evolution shaped by reticulations.

Purpose of the Study:

  • To develop algorithms for inferring optimal displayed trees from gene trees and tree-child networks.
  • To compute lower bounds for displayed tree costs under deep coalescence and duplication costs.
  • To provide methods for verifying exact solutions and resolving conflicting reticulation edges.

Main Methods:

  • A dynamic programming (DP) algorithm with O(mn) time complexity for computing lower bounds.
  • A conflict resolution algorithm utilizing DP invocations.
  • Algorithms for level-k tree-child networks and branch and bound solutions.
  • Extension of algorithms to broader classes of phylogenetic networks.

Main Results:

  • An O(mn) DP algorithm computes a lower bound for optimal displayed tree cost and verifies exactness.
  • A conflict resolution algorithm is proposed, requiring O(r) DP calls.
  • Efficient algorithms for level-k networks and branch and bound solutions are presented.
  • Simulated data shows average runtimes of O(mn) for deep coalescence and O(mn) for duplication costs.

Conclusions:

  • Algorithms perform well on empirical and simulated data, outperforming enumeration strategies.
  • Efficiently resolve internal dissimilarities between gene trees and networks.
  • Enable analysis of complex phylogenetic networks with numerous reticulations.