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Phylogenetic trees Level 3 Molecular Evolution and Bioinformatics Jim Provan Page and Holmes: Chapter 2
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Tree terminology A phylogenetic tree depicts evolutionary relationships A tree consists of nodes connected by branches Nodes and branches of a tree have different kinds of information associated with them: Some phylogenetic methods reconstruct characters of hypothetical ancestors Most estimate amount of evolution (branch length) Terminal node / terminal taxon / OTU Internal node / hypothetical ancestor Root Branch
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Trees are like mobiles ABCDABCD = ABCD =
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Polytomies Star tree Partially resolved Fully resolved “Hard” polytomy ? “Soft” polytomy
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A shorthand for trees EDCBA (((A,B),C),(D,E))
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Information in trees ABCCladogramA B C 4 1 22 Additive tree ABC Ultrametric tree Simply shows relative recency of common ancestry Contains extra information, namely branch lengths (evolutionary change) Depicts evolutionary time
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Rooted and unrooted trees A rooted tree has a node from which all other nodes descend: It has a “direction”: the closer a node is to the root, the older it is in time It allows the definition of ancestor-descendent relationships Unrooted trees do not specify evolutionary relationships in the same way HCGOB H C G O B
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Numbers of rooted and unrooted trees The number of unrooted trees U n for n sequences is given by U n = (2n – 5)(2n – 7)... (3)(1) U n = (2n – 5)(2n – 7)... (3)(1) The number of rooted trees R n for n sequences is given by R n = (2n – 3)(2n – 5)... (3)(1) R n = (2n – 3)(2n – 5)... (3)(1) = (2n – 3) U n = (2n – 3) U nn2345678910 U n 11315105949 10 395 135 135 2 027 025 R n 1315105949 10 395 135 135 2 027 025 34 459 425 20 8 200 794 532 637 891 559 000
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Terminology of patterns of ancestral and derived character states ApomorphyPlesiomorphyAutapamorphy SynapomorphyHomoplasy
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Ancestors Phylogenies presuppose ancestors: Extinct organisms that left descendents which comprise modern species Represented by internal nodes of a tree Generally hypothetical and inferred from extant sequences Two recent developments have provided new problems in dealing with ancestors: Recovery of DNA from extinct taxa Viral sequences which evolve quickly enough to be tracked in “real time” Cladists have adopted the convention that extinct taxa lacking autapomorphies are ancestral
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Metric distances In order for a distance measure to be used for building phylogenies, it must be a metric and it must be additive A distance d between two sequences, a and b, is a metric if it satisfies these properties: d(a,b) 0(non-negativity) d(a,b) = d(b,a) (symmetry) d(a,c) d(a,b) + d(b,c)(triangle inequality) d(a,b) = 0 if and only if a = b(distinctness) In general, conditions 1, 2 and 4 are true for all measures of dissimilarity calculated directly from sequences
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Ultrametric and additive distances A metric is an ultrametric if it satisfies the additional criterion that: d(a,b) maximum [d(a,c), d(b,c)] Ultrametric distances have the very useful evolutionary property of implying a constant rate of evolution: Idea of a molecular clock Relative rate test is a measure of how far pairwise differences between three sequences depart from ultrametricity To be additive, a measure must also satisfy the four- point condition: d(a,b) + d(c,d) maximum [d(a,c) + d(b,d), d(a,d) + d(b,c)] Of the three sums, the two largest must be equal
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2 6 6 10 An ultrametric distance matrix ABCD2610A610B10CD A B C D11 2 3 5 2
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6 7 3 14 10 9 An additive distance matrix ABCD6714A310B9CD A B C D51 1 1 6 2
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Monophyletic Non-monophyletic Clades and classification
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Non-monophyletic groups BirdsCrocodilesLizardsTurtles New World vulturesStorks Birds of prey Old World vultures Reptiles VulturesParaphyleticPolyphyletic
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Consensus trees HCGOBHCGOB HCGOB
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ABCDEABCDEABCDE ABCDEStrictABCDEMajority-rule67 100 67
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