Models of Molecular Evolution III Level 3 Molecular Evolution and Bioinformatics Jim Provan Page and Holmes: Sections 7.5 – 7.8.

Slides:



Advertisements
Similar presentations
Neutral Theory of Molecular Evolution most base substitutions are selectively neutral drift dominates evolution at the molecular level Under drift, rate.
Advertisements

R ATES OF P OINT M UTATION. The rate of mutation = the number of new sequence variants arising in a predefined target region per unit time. Target region.
Chapter 19 Evolutionary Genetics 18 and 20 April, 2004
Random fixation and loss of heterozygosity
Exam Thursday Covers material through Today’s lecture Practice problems and answers are posted Bring a calculator 5 questions, answer your favorite 4 Please.
Change in frequency of the unbanded allele (q) as a function of q for island populations. Equilibrium points a)Strong selection for q, little migration.
Plant of the day! Pebble plants, Lithops, dwarf xerophytes Aizoaceae
Atelier INSERM – La Londe Les Maures – Mai 2004
Population size does not influence mitochondrial genetic diversity in animals E. Bazin, S. Glémin, N. Galtier CNRS UMR 5171 – Génome, Populations, Interactions,
Molecular evolution:   how do we explain the patterns of variation observed in DNA sequences? how do we detect selection by comparing silent site substitutions.
14 Molecular Evolution and Population Genetics
Genetica per Scienze Naturali a.a prof S. Presciuttini Human and chimpanzee genomes The human and chimpanzee genomes—with their 5-million-year history.
From population genetics to variation among species: Computing the rate of fixations.
SOME PATTERNS OF MOLECULAR EVOLUTION AND VARIATION 1. Regions of the genome with unusually low rates of genetic recombination seem to have low levels of.
1 Mendelian Genetics in Populations II Migration, Genetic Drift, and Nonrandom Mating.
BIOE 109 Summer 2009 Lecture 6- Part II Molecular evolution.
Molecular Evolution with an emphasis on substitution rates Gavin JD Smith State Key Laboratory of Emerging Infectious Diseases & Department of Microbiology.
Evolutionary Genome Biology Gabor T. Marth, D.Sc. Department of Biology, Boston College Medical Genomics Course – Debrecen, Hungary, May 2006.
Scott Williamson and Carlos Bustamante
Molecular Clocks, Base Substitutions, & Phylogenetic Distances.
CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Molecular Evolution Course #27615 Anders Gorm Pedersen Molecular Evolution Group Center for Biological Sequence.
Adaptive Molecular Evolution Nonsynonymous vs Synonymous.
TGCAAACTCAAACTCTTTTGTTGTTCTTACTGTATCATTGCCCAGAATAT TCTGCCTGTCTTTAGAGGCTAATACATTGATTAGTGAATTCCAATGGGCA GAATCGTGATGCATTAAAGAGATGCTAATATTTTCACTGCTCCTCAATTT.
Biodiversity IV: genetics and conservation
Chapter 3 Substitution Patterns Presented by: Adrian Padilla.
- any detectable change in DNA sequence eg. errors in DNA replication/repair - inherited ones of interest in evolutionary studies Deleterious - will be.
Molecular Clock. Rate of evolution of DNA is constant over time and across lineages Resolve history of species –Timing of events –Relationship of species.
Lecture 21: Tests for Departures from Neutrality November 9, 2012.
Mechanisms of Evolution. I. Natural Selection & Charles Darwin  Charles Darwin ( ) an English scientist considered the founder of the evolutionary.
Part VI and Chapter 20 Biology Sixth Edition Raven/Johnson (c) The McGraw-Hill Companies, Inc.
Models of Molecular Evolution I Level 3 Molecular Evolution and Bioinformatics Jim Provan Page and Holmes: Sections 7.1 – 7.2.
Evolution Chapters Evolution is both Factual and the basis of broader theory What does this mean? What are some factual examples of evolution?
Models of Molecular Evolution II Level 3 Molecular Evolution and Bioinformatics Jim Provan Page and Holmes: Sections 7.3 – 7.4.
Is heterozygosity common or rare? Sewell Wright Theodosius Dobzhansky.
Deviations from HWE I. Mutation II. Migration III. Non-Random Mating IV. Genetic Drift V. The Neutral Theory.
The Biology and Genetic Base of Cancer. 2 (Mutation)
Rates and Fitness Effects of Mutations Adam Eyre-Walker (University of Sussex)
1 Genome Evolution Chapter Introduction Genomes contain the raw material for evolution; Comparing whole genomes enhances – Our ability to understand.
Calculating branch lengths from distances. ABC A B C----- a b c.
Chapter 24: Molecular and Genomic Evolution CHAPTER 24 Molecular and Genomic Evolution.
Introduction to History of Life. Biological evolution consists of change in the hereditary characteristics of groups of organisms over the course of generations.
Cédric Notredame (08/12/2015) Molecular Evolution Cédric Notredame.
Selectionist view: allele substitution and polymorphism
Table 8.3 & Alberts Fig.1.38 EVOLUTION OF GENOMES C-value paradox: - in certain cases, lack of correlation between morphological complexity and genome.
Lecture 20 : Tests of Neutrality
NEW TOPIC: MOLECULAR EVOLUTION.
Molecular evolution Part I: The evolution of macromolecules.
Objective: Chapter 23. Population geneticists measure polymorphisms in a population by determining the amount of heterozygosity at the gene and molecular.
The plant of the day Pinus longaevaPinus aristata.
Testing the Neutral Mutation Hypothesis The neutral theory predicts that polymorphism within species is correlated positively with fixed differences between.
Evolutionary Genome Biology Gabor T. Marth, D.Sc. Department of Biology, Boston College
Single Nucleotide Polymorphisms (SNPs) By Amira Jhelum Rahul Shweta.
In populations of finite size, sampling of gametes from the gene pool can cause evolution. Incorporating Genetic Drift.
Modelling evolution Gil McVean Department of Statistics TC A G.
Evolution of populations Ch 21. I. Background  Individuals do not adapt or evolve  Populations adapt and evolve  Microevolution = change in allele.
Chapter 8 Genome Evolution
The neutral theory of molecular evolution
Neutrality Test First suggested by Kimura (1968) and King and Jukes (1969) Shift to using neutrality as a null hypothesis in positive selection and selection.
Human Chimp How does DNA evolve? Nucleotide substitutions
Fig. 1. (a) Relationship of codon adaptation index (CAI) and the number of substitutions per fourfold-degenerate site (dS) between D. melanogaster.
The Neutral Theory M. Kimura, 1968
15-2 Mechanisms of Evolution
What are the Patterns Of Nucleotide Substitution Within Coding and
Testing the Neutral Mutation Hypothesis
1. "HARD" Selection can 'cost' a population individuals:
Molecular Clocks Rose Hoberman.
26.5 Molecular Clocks Help Track Evolutionary Time
Evolution Standards Rachel Tumlin.
Evolution by Genetic Drift : Main Points (p. 231)
Evolution by Genetic Drift : Main Points (p. 231)
Presentation transcript:

Models of Molecular Evolution III Level 3 Molecular Evolution and Bioinformatics Jim Provan Page and Holmes: Sections 7.5 – 7.8

The nearly neutral theory Variable rates of nucleotide substitution Variable rates of nucleotide substitution Variable mutation rates (generation time, metabolic rate, DNA repair) Nearly neutral mutations (population size and weak selection)

Development of the nearly neutral theory By the early 1970s it was becoming clear that: Some amino acid substitution rates were inconsistent with a Poisson clock Levels of heterozygosity were not as high as expected in natural populations Tomoko Ohta suggested that most non-synonymous changes were not perfectly neutral Deleterious Advantageous Neutral Slightly deleterious Slightly advantageous

Development of the nearly neutral theory Nearly neutral mutations are those where the product of the population size and the selection coefficient is near zero i.e. Ns  0 These changes are subject to weak natural selection as well as genetic drift Rate of substitution (per year) for nearly neutral mutations will depend on population size, selective coefficient and mutation rate, set to generation time Mutations at non-coding and synonymous sites are still neutral Relative importance of selection or genetic drift and hence probability of fixation depends on population size

The nearly neutral theory and real time molecular clocks Long generation time (lower mutation rate) Small population size (higher probability of fixation) + Short generation time (higher mutation rate) Large population size (lower probability of fixation) + ~ Real time molecular clock ~ Real time molecular clock

The nearly neutral theory and real time molecular clocks A study of 20 mammalian genes showed that R(t) values were generally well over 1.0, rejecting the Poisson clock After correcting for generation time and lineage effects: Average R(t) for synonymous sites dropped from 14.4 to 4.6 Average R(t) for non-synonymous sites only dropped from 8.26 to 6.95 Most variation in synonymous sites is due to lineage effects Non-synonymous rates are less generation time dependent than synonymous sites

Testing the neutral theory within species Neutral theory makes two very important predictions about levels of genetic variation within species: Extent of polymorphism is a function only of the population size (N) and the mutation rate (  ) Levels of polymorphism are correlated with amount of variation between species i.e. genes that evolve slowly between species also exhibit low variation within a species Original allozyme studies cast doubt on these predictions: Levels of heterozygosity were found to be too low Difficult to draw firm conclusions, since N and  are hard to quantify, and allozymes underestimate diversity levels Best to test theories at the DNA level

Testing the neutral theory within species Important assessment of the neutral theory is to test proposed correlation between levels of within species polymorphism and between species divergence: If synonymous and non-synonymous substitutions are neutral then ratio of both types of change will be the same within and between species because they result from the same neutral mutation process Positive natural selection would alter this ratio because an advantageous non-synonymous mutation would be fixed quicker by natural selection i.e. be a polymorphism for less time, leading to less within-species non-synonymous variation than expected given levels detected between species

Patterns of substitution at the Adh locus in Drosophila D. melanogaster D. simulans D. yakuba 2/140/110/17 1/21/05/15 SynonymousNon-synonymousFixed177Polymorphic422 G = 7.43 P = 0.006

Recombination and DNA polymorphism in Drosophila Most dramatic example of incompatibility between levels of variation between and within a species occurs in regions of the Drosophila genome where recombination rates are low: Distal tip of the X chromosome Small chromosome IV Neutralist explanation is that these regions have either lower mutation rates or are under selective constraint If this is the case, these regions should also show reduced levels of variation between species

Recombination and DNA polymorphism in Drosophila The yellow-achaete (y, ac) region on the X chromosome of D. melanogaster has a reduced level of polymorphism Extent of divergence in this region between D. melanogaster and D. simulans (5.4%) is similar to that observed in other genes (average 4.7%) – this contradicts the neutral theory Natural selection can explain this discrepancy through the dual action of selective sweeps and genetic hitchhiking

Hitchhiking and selective sweeps Time t1t1t1t1 t2t2t2t2 t3t3t3t3 t4t4t4t4

Can we resolve the neutralist- selectionist debate? Most support for neutral theory has come from comparisons of genes across distantly related species Natural selection is more apparent over shorter time scales As time proceeds, fixation due to selection may be obscured by neutral mutations Majority of original selection events in adaptive radiations e.g. mammals Overall, it seems reasonable to conclude that both selection and drift shape evolutionary fate of mutations: Majority of substitutions do not affect fitness (neutralist) The “footprints” of natural selection are still evident in more recently evolved levels, particularly at non-synonymous sites