Maximum Likelihood Molecular Clock Comb: Analytic Solutions

Maximum likelihood (ML) is increasingly used as an optimality criterion for selecting evolutionary trees, but finding the global optimum is a hard computational task. Because no general analytic solution is known, numeric techniques such as hill climbing or expectation maximization (EM), are used in order to find optimal parameters for a given tree. So far, analytic solutions were derived only for the simplest model--three taxa, two state characters, under a molecular clock. Four taxa rooted trees have two topologies--the fork (two subtrees with two leaves each) and the comb (one subtree with three leaves, the other with a single leaf). In a previous work, we devised a closed form analytic solution for the ML molecular clock fork. In this work, we extend the state of the art in the area of analytic solutions ML trees to the family of all four taxa trees under the molecular clock assumption. The change from the fork topology to the comb incurs a major increase in the complexity of the underlying algebraic system and requires novel techniques and approaches. We combine the ultrametric properties of molecular clock trees with the Hadamard conjugation to derive a number of topology dependent identities. Employing these identities, we substantially simplify the system of polynomial equations. We finally use tools from algebraic geometry (e.g., Gröbner bases, ideal saturation, resultants) and employ symbolic algebra software to obtain analytic solutions for the comb. We show that in contrast to the fork, the comb has no closed form solutions (expressed by radicals in the input data). In general, four taxa trees can have multiple ML points. In contrast, we can now prove that under the molecular clock assumption, the comb has a unique (local and global) ML point. (Such uniqueness was previously shown for the fork.).

[1]  T. Jukes CHAPTER 24 – Evolution of Protein Molecules , 1969 .

[2]  Barbara R. Holland,et al.  Multiple maxima of likelihood in phylogenetic trees: an analytic approach , 2000, RECOMB '00.

[3]  Michael D. Hendy,et al.  Analytic Solutions for Three-Taxon MLMC Trees with Variable Rates Across Sites , 2001, WABI.

[4]  D. Penny,et al.  Spectral analysis of phylogenetic data , 1993 .

[5]  Sagi Snir,et al.  Molecular clock fork phylogenies: closed form analytic maximum likelihood solutions. , 2004, Systematic biology.

[6]  Sagi Snir,et al.  Analytic solutions of maximum likelihood on forks of four taxa. , 2007, Mathematical biosciences.

[7]  Z. Yang,et al.  Complexity of the simplest phylogenetic estimation problem , 2000, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[8]  I. M. Gelʹfand,et al.  Discriminants, Resultants, and Multidimensional Determinants , 1994 .

[9]  B. Chor,et al.  Multiple maxima of likelihood in phylogenetic trees: an analytic approach , 2000, RECOMB '00.

[10]  Mike Steel,et al.  The Maximum Likelihood Point for a Phylogenetic Tree is Not Unique , 1994 .

[11]  M. Kimura,et al.  The neutral theory of molecular evolution. , 1983, Scientific American.

[12]  J. Neyman MOLECULAR STUDIES OF EVOLUTION: A SOURCE OF NOVEL STATISTICAL PROBLEMS* , 1971 .

[13]  D Penny,et al.  A discrete Fourier analysis for evolutionary trees. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[14]  D. Mumford Algebraic Geometry I: Complex Projective Varieties , 1981 .

[15]  Sagi Snir,et al.  Maximum likelihood on four taxa phylogenetic trees: analytic solutions , 2003, RECOMB '03.