Population Genetics Subfield of Genetics Subject is genetic differences within and between populations Part of evolutionary biology Population Genetics Genetics definition • Genetics is the study of genes, genetic variation, and heredity in living organisms. Genes A gene is a sequence of DNA or RNA It codes for a molecule that has a biological function Alleles • An allele is a variant form of a given gene • Different alleles can result in different observable phenotypic traits, e.g. different pigmentation and color variation in Gregor Mendel's discovery that the white and purple flower colors in pea plants were the result of "pure line" traits which could be used as a control for future experiments • Many genetic variations result in little or no observable variation. The word "allele" is a short form Population Genetics Examine phenomena • population structure • adaptation • speciation Population Genetics • Founders were Sewall Wright, J. B. S. Haldane and Ronald Fisher • Evolutionary synthesis • Mathematical discipline • Theoretical • Laboratory • Field Population Genetics • Models are used both for statistical inference from DNA sequence data and for proof/disproof of concept • Phenotypic approaches to modelling evolution • Evolutionary game theory • Adaptive dynamics Population Genetics • Genetic phenomena • Dominance • Epistasis • Genetic recombination and linkage disequilibrium Epistasis • Phenomenon that consists of the effect of one gene being dependent on the presence of one or more 'modifier genes' (genetic background) • Epistatic mutations have different effects in combination than individually • Concept from genetics, biochemistry, population genetics, computational biology and evolutionary biology Epistasis • The gene for total baldness is epistatic to those for blond hair or red hair. The haircolour genes are hypostatic to the baldness gene. The baldness phenotype supersedes genes for hair colour and so the effects are non-additive Population Genetics • Population genetics began as a reconciliation of Mendelian inheritance and biostatistics models. Natural selection will only cause evolution if there is enough genetic variation in a population. • The Hardy–Weinberg principle provides the solution to how variation is maintained in a population with Mendelian inheritance. • According to this principle, the frequencies of alleles (variations in a gene) will remain constant in absence of selection, mutation, migration or genetic drift. Key Points What is population genetics? How to describe genetic structures? The Hardy-Weinberg Law. Factors that disturb Hardy-Weinberg equilibrium. Consanguinity. Population Genetics • genetic structure of a population • alleles • genotypes group of individuals of the same species that can interbreed Population Genetics • Is the quantitative study of the distribution of genetic variation in populations and of how the frequencies of genes and genotypes are maintained or change. Describing genetic structure • genotype frequencies • allele frequencies rr = white Rr = pink RR = red Describing genetic structure • genotype frequencies • allele frequencies 200 white 500 pink genotype frequencies: 200/1000 = 0.2 rr 500/1000 = 0.5 Rr 300 red total = 1000 flowers 300/1000 = 0.3 RR Describing genetic structure • genotype frequencies • allele frequencies 200 rr = 400 r 500 Rr = 500 r = 500 R 300 RR = 600 R allele frequencies: 900/2000 = 0.45 r 1100/2000 = 0.55 R total = 2000 alleles (gene pool) • Gene pool is a collection of all the alleles at a particular locus for the entire population. • For autosomal loci, the size of the gene pool at one locus is twice the number of individuals in the population. For example: HIV resistance---ΔCCR5 Number of People Observed Relative Genotype Frequency Allele CCR5/CCR5 647 647/788=0.821 CCR5 CCR5/ ΔCCR5 134 134/788=0.170 Genotype ΔCCR5/ ΔCCR5 Total 7 788 7/788=0.009 1.000 Derived Allele Frequencies (2X647)+(1X134) 788X2 =0.906 ΔCCR5 (2X7)+(1X134) 788X2 =0.094 another way to calculate allele frequencies: • from genotype frequency • F(CCR5)=0.821+0.170/2=0.906 • F(ΔCCR5)=0.009+0.170/2=0.094 • Can we calculate the proportion of the population with various genotypes once we know the allele frequencies ? The Hardy-Weinberg Law Geoffrey Hardy Wilhelm Weinberg An English mathematician A German physician The Hardy-Weinberg Law The frequency of the three genotypes AA, Aa and aa is given by the terms of the binomial expansion of (p+q)2=p2+2pq+q2. The population genotype frequencies from generation to generation will remain constant, at equilibrium, if the allele frequencies p and q remain constant. Where p = frequency of “dominant” allele and q = frequency of “recessive” allele Proof of the equilibrium • • • • Gametes A (p) a (q) A (p) AA (pXp) Aa (pXq) a (q) Aa (pXq) Aa (qXq) Frequency of AA offspring is then p2; Frequency of aa offspring is then q2 ; Frequency of Aa offspring then 2pq ; Frequency of an allele being present is = 1. AA :Aa :aa = p2 :2pq:q2 Proof of the equilibrium Types of Matings Mother Father AA AA AA Offspring Frequency AA Aa p2X p2= p4 (p4) Aa p2X2pq= 2p3q ½(2p3q) ½(2p3q) Aa AA 2pqXp2= 2p3q ½(2p3q) ½(2p3q) AA aa p2Xq2= p2q2 (p2q2) aa AA q2Xp2 = p2q2 (p2q2) Aa Aa 2pqX2pq=4p2q2 Aa aa aa aa ¼(4p2q2) aa ½(4p2q2) ¼(4p2q2) 2pqXq2=2pq3 ½(2pq3) ½(2pq3) Aa q2X2pq=2pq3 ½(2pq3) ½(2pq3) aa q2Xq2=q4 AA:p4+2p3q+p2q2=p2(p2+2pq+q2)=p2 Aa: 2p3q +2p2q2 + 2p2q2 + 2pq3 =2pq (p2+2pq+q2)=2pq aa: p2q2 +2pq3+q4=q2(p2+2pq+q2)=q2 (q4) Hardy-Weinberg Equilibrium AA :Aa :aa = p2 :2pq:q2 Conditions or assumptions for the Hardy – Weinberg law to be true… • Infinitely large population • Randomly mating population • No mutation • No migration • No natural selection • Frequencies of alleles do not change over time The Hardy-Weinberg Law in Autosomal Recessive Disease • For example, the frequency of Albinism is approximately 1/10000. • Q: What are the gene frequency and the heterozygote frequency of it? • The frequency of affected individuals=1/10000=q2 • q=1/100=0.01 (the frequency of allele a) • p=1-q=0.99 (the frequency of allele A) • 2pq = 2X0.99X0.01 ≈ 0.02 (the carrier frequency) There would be an approximately 2% chance that a parent known to be a carrier of Albunism. The Hardy-Weinberg Law in Autosomal Dominant Disease • For example, the frequency of retinoblastoma is approximately 1/10000. • Q: What are the gene frequency of mutant rb? • The frequency of dominant allele in AD disease is very low, so p2 is too small to be estimated. • The frequency of affected individuals=1/10000=2pq • 2p ≈1/10000 (because q≈1) • p=1/20000 (the frequency of mutant rb allele) The Hardy-Weinberg Law in X-linked Dominant Disease • Affected male: XAY (p) • Affected female: XAXA (p2) and XAXa (2pq) • P2+2pq ≈ 2p • So, the affected incidence in female is twice than in male. The Hardy-Weinberg Law in X-linked Recessive Disease • For example, the frequency of red-green color blindness is approximately 8% in males. Sex Genotype Phenotype Male X+ Normal Xcb Color blind X+/X+ Normal X+/Xcb Normal Xcb/Xcb Color blind Female Incidence (Approximate) q=0.08 The Hardy-Weinberg Law in X-linked Recessive Disease Sex Genotype Phenotype Incidence (Approximate) Male X+ Normal p=0.92 Xcb Color blind q=0.08 X+/X+ Normal p2=(0.92)2 X+/Xcb Normal 2pq=2(0.92)(0.08) Xcb/Xcb Color blind q2=(0.08)2 Female Factors that disturb Hardy-Weinberg equilibrium • mutation • migration • natural selection • genetic drift • non-random mating Factors that disturb Hardy-Weinberg equilibrium • mutation spontaneous change in DNA • migration • natural selection • creates new alleles • ultimate source of all genetic variation • genetic drift • non-random mating Factors that disturb Hardy-Weinberg equilibrium • mutation • migration individuals move into population new alleles • natural selection • introduces “gene flow” • genetic drift • non-random mating Factors that disturb Hardy-Weinberg equilibrium • mutation • migration certain genotypes produce more offspring • natural selection • genetic drift • differences in survival or reproduction differences in“fitness” • leads to adaptation • non-random mating Fitness and Coefficient of Seletion • Fitness is the chief factor that determines whether a mutation is lost immediately, becomes stable in the population, or even becomes, over time, the predominant allele at the locus concerned. • Whether an allele is transmitted to the succeeding generation depends on its fitness (f). Fitness and Coefficient of Seletion Fitness (f)--- is a measure of the number of offspring of affected persons who survive to reproductive age, compared with an appropriate control group. Coefficient of selection (s) --- is a measure of the loss of fitness and is defined as 1-f, that is, the proportion of mutant alleles that are not passed on and are therefore lost as a result of selection. Selection on sickle-cell allele aa – abnormal ß hemoglobin very low fitness sickle-cell anemia AA – normal ß hemoglobin vulnerable to malaria Aa – both ß hemoglobins resistant to malaria intermed. fitness high fitness Selection favors heterozygotes (Aa). Both alleles maintained in population (a at low level). Factors that disturb Hardy-Weinberg equilibrium • mutation • migration genetic change by chance alone • natural selection • genetic drift • non-random mating • sampling error • misrepresentation • small populations Genetic Drift Genetic drift Before: 8 RR 0.50 R 8 rr 0.50 r After: 2 RR 6 rr 0.25 R 0.75 r Founder Effect • The founder effect is the loss of genetic variation that occurs when a new population is established by a very small number of individuals from a larger population. • As a result of the loss of genetic variation, the new population may be distinctively different, both genetically and phenotypically, from the parent population from which it is derived. Founder Effect Ellis-van Creveld syndrome Factors that disturb Hardy-Weinberg equilibrium • mutation • migration • natural selection • genetic drift • non-random mating cause changes in allele frequencies Factors that disturb Hardy-Weinberg equilibrium • mutation • migration • natural selection mating combines alleles into genotypes • genetic drift • non-random mating • non-random mating non-random allele combinations A A A A A a A A a A A 0.8 AA A 0.8 0.8 x 0.8 a aA 0.2 0.2 x 0.8 aa x aa aa a 0.2 Aa 0.8 x 0.2 aa 0.2 x 0.2 AA x AA AA allele frequencies: A = 0.8 A = 0.2 genotype frequencies: AA = 0.8 x 0.8 = 0.64 Aa = 2(0.8 x0.2) = 0.32 aa = 0.2 x 0.2 = 0.04 Consanguinity • Couples are related and have one or more ancestors in common. • Consanguinity is arbitrarily as a union of individuals related to each other as close as or closer than second cousins. Coefficient of inbreeding • Consanguinity is measured by the coefficient of inbreeding (F) : • Is the probability that a homozygote has received both alleles at a locus from the same ancestral source Coefficient of inbreeding of AR genes A 1A2 A3A4 A1A1 = (1/2)4 P2 P1 A2A2 = (1/2)4 A3A3 = (1/2)4 B2 B1 ◇ A4A4 = (1/2)4 F = 4 ×(1/2)4 = 1 / 4 S Brother-sister Coefficient of inbreeding of AR genes A1A2 A1A1 = (1/2)5 A3A4 P2 P1 A2A2 = (1/2)5 A3A3 = (1/2)5 B2 B1 C ◇ S A4A4 = (1/2)5 F = 4 ×(1/2)5 = 1 / 8 Uncle-niece Coefficient of inbreeding of AR genes A1A2 P1 □ A3A4 ○ P2 □ B1○ ○B2 A1A1 = (1/2)6 □ A2A2 = (1/2)6 A3A3 = (1/2)6 C1□ ○ C2 ◇ S A1A1 A2A2 A3A3 A4A4 A4A4 = (1/2)6 F = 4 ×(1/2)6 = 1 / 16 First cousins Coefficient of inbreeding of X-linked genes • Remember that sons receive their X chromosome from their mother and have to pass on their X chromosome to their daughter. Coefficient of inbreeding of X-linked genes X1Y P1 □ X2X3 ○ P2 □ B1○ □B2 C1□ ○ C2 ○ S X1X1 X2X2 X3X3 X1 X1 = 0 ○ X2X2 = (1/2)4 X3X3 = (1/2)4 F = (1/2)4+(1/2)4= 1 / 8 Coefficient of inbreeding of X-linked genes X 1Y X2X3 P2 P1 X1X1 = (1/2)3 X2X2 = (1/2)5 B1 B2 C1 C2 S X3X3 = (1/2)5 F = (1/2)3+(1/2)5 +(1/2)5 = 3 / 16 Coefficient of inbreeding of X-linked genes F = 0 Key Points What is population genetics? How to destribe genetic structures? The Hardy-Weinberg Law. Factors that disturb Hardy-Weinberg equilibrium. Consanguinity. Question 9 (on p207) • You are consulted by a couple, Abby and Andrew, who tell you that Abby’s sister Anna has Hurler syndrome (an AR disease) and that they are concerned that they themselves might have a child with the same disorder. The population incidence of Hurler syndrome is about 1/90000 in your community. • A. If Abby and Andrew are not consanguineous, what is the risk that Abby and Andrew’s first child will have Hurler syndrome? • B. If they are first cousins, what is the risk? A Abby: the chance of being a carrier = 2/3 Andrew: the chance of being a carrier = 1/150 (2pq) The risk of having an affected child = 2/3 X 1/150 X 1/4 = 1/900 B Abby: the chance of being a carrier = 2/3 Andrew: the chance of being a carrier = 1/4 The risk of having an affected child = 2/3 X 1/4 X 1/4 = 1/24