1 / 48

Introduction to Genetic Theory

Introduction to Genetic Theory. Pak Sham Twin Workshop, March 2003. Aims. To introduce Mendel’s law and describe its consequences for genetic relationships To describe how the covariance structure of family data is influenced by genetic factors

wpaladino
Download Presentation

Introduction to Genetic Theory

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Introduction to Genetic Theory Pak Sham Twin Workshop, March 2003

  2. Aims • To introduce Mendel’s law and describe its consequences for genetic relationships • To describe how the covariance structure of family data is influenced by genetic factors • To describe how allele-sharing at QTL influences the covariance between relatives

  3. Mendel’s Experiments AA aa Pure Lines F1 Aa Aa Intercross Aa Aa aa AA 3:1 Segregation Ratio

  4. Mendel’s Experiments F1 Pure line Aa aa Back cross Aa aa 1:1 Segregation ratio

  5. A1 A2 ½ ½ Mendel’s Law of Segregation Parental genotype Meiosis/Segregation Gametes A1 A2

  6. Maternal A3 A4 ½ ½ A1 A1 A3 A4 ½ ¼ ¼ A1 Paternal A2 A2 A2 A3 A4 ½ ¼ ¼ Mendel’s Law of Segregation

  7. Identity by Descent (IBD) • Two alleles are IBD if they are descended from and replicates of the same ancestral allele 2 1 aa Aa 3 4 5 6 AA Aa Aa Aa 7 8 AA Aa

  8. IBD: Parent-Offspring AB CD AC If the parents are unrelated, then parent-offspring pairs always share 1 allele IBD

  9. IBD: MZ Twins AB CD AC AC MZ twins always share 2 alleles IBD

  10. IBD: Half Sibs AB CD EE AC CE/DE IBD Sharing Probability 0 ½ 1 ½

  11. IBD: Full Sibs IBD of paternal alleles 0 1 0 IBD of maternal alleles 1

  12. IBD: Full Sibs IBD Sharing Probability 0 1/4 1 1/2 21/4 Average IBD sharing = 1

  13. Genetic Relationships  (kinship coefficient): Probability of IBD between two alleles drawn at random, one from each individual, at the same locus. : Probability that both alleles at the same locus are IBD Relationship   MZ twins 0.5 1 Parent-offspring 0.25 0 Full sibs 0.25 0.25 Half sibs 0.125 0

  14. Proportion of Alleles IBD () Proportion of alleles IBD = Number of alleles IBD / 2 Relatiobship  E() Var() MZ 0.5 1 0 Parent-Offspring 0.25 0.5 0 Full sibs 0.25 0.5 0.125 Half sibs 0.125 0.25 0.0625 Most relationships demonstrate variation in  across the chromosomes

  15. Quantitative Traits • Mendel’s laws of inheritance apply to complex traits influenced by many genes • Polygenic Model: • Multiple loci each of small and additive effects • Normal distribution of continuous variation

  16. 1 Gene  3 Genotypes  3 Phenotypes 2 Genes  9 Genotypes  5 Phenotypes 3 Genes  27 Genotypes  7 Phenotypes 4 Genes  81 Genotypes  9 Phenotypes Quantitative Traits Central Limit Theorem  Normal Distribution

  17. Biometrical Genetic Model Genotype means 0 AA m + a -a +a d Aa m + d aa m – a

  18. Continuous Variation 95% probability 2.5% 2.5% -1.96 1.96 0 Normal distribution Mean , variance 2

  19. Bivariate normal

  20. Familial Covariation Bivariate normal disttribution Relative 2 Relative 1

  21. Means, Variances and Covariances

  22. Covariance Algebra Forms Basis for Path Tracing Rules

  23. Covariance and Correlation Correlation is covariance scaled to range [-1,1]. For two traits with the same variance: Cov(X1,X2) = r12 Var(X)

  24. Genotype Frequencies (random mating) A a A p2 pqp a qpq2 q p q Hardy-Weinberg frequencies p(AA) = p2 p(Aa) = 2pq p(aa) = q2

  25. Biometrical Model for Single Locus Genotype AA Aa aa Frequency p2 2pq q2 Effect (x) a d -a Residual var2 2 2 Mean m = p2(a) + 2pq(d) + q2(-a) = (p-q)a + 2pqd

  26. Single-locus Variance under Random Mating Genotype AA Aa aa Frequency p2 2pq q2 (x-m)2 (a-m)2 (d-m)2 (-a-m)2 Variance = (a-m)2p2 + (d-m)22pq + (-a-m)2q2 = 2pq[a+(q-p)d]2 + (2pqd)2 = VA + VD

  27. Average Allelic Effect Effect of gene substitution: a  A If background allele is a, then effect is (d+a) If background allele is A, then effect is (a-d) • Average effect of gene substitution is therefore • = q(d+a) + p(a-d) = a + (q-p)d Additive genetic variance is therefore VA = 2pq2

  28. a d m -a Additive and Dominance Variance aa Aa AA Total Variance = Regression Variance + Residual Variance = Additive Variance + Dominance Variance

  29. Cross-Products of Deviations for Pairs of Relatives AA Aa aa AA (a-m)2 Aa (a-m)(d-m) (d-m)2 aa (a-m)(-a-m) (-a-m)(d-m) (-a-m)2 The covariance between relatives of a certain class is the weighted average of these cross-products, where each cross-product is weighted by its frequency in that class.

  30. Covariance of MZ Twins AA Aa aa AA p2 Aa 0 2pq aa 0 0 q2 Covariance = (a-m)2p2 + (d-m)22pq + (-a-m)2q2 = 2pq[a+(q-p)d]2 + (2pqd)2 = VA + VD

  31. Covariance for Parent-offspring (P-O) AA Aa aa AA p3 Aa p2q pq aa 0 pq2 q3 Covariance = (a-m)2p3 + (d-m)2pq + (-a-m)2q3 + (a-m)(d-m)2p2q+ (-a-m)(d-m)2pq2 = pq[a+(q-p)d]2 = VA / 2

  32. Covariance for Unrelated Pairs (U) AA Aa aa AA p4 Aa 2p3q 4p2q2 aa p2q2 2pq3 q4 Covariance = (a-m)2p4 + (d-m)24p2q2 + (-a-m)2q4 + (a-m)(d-m)4p3q+ (-a-m)(d-m)4pq3 + (a-m)(-a-m)2p2q2 = 0

  33. IBD and Correlation • IBD  perfect correlation of allelic effect • Non IBD  zero correlation of allelic effect # alleles IBD Correlation at each locus Allelic Dom. MZ 2 1 1 P-O 1 0.5 0 U 0 0 0

  34. Covariance for DZ twins • Genotype frequencies are weighted averages: • ¼ MZ twins • ½ Parent-offspring • ¼ Unrelated • Covariance = ¼(VA+VD) + ½(VA/2) + ¼ (0) = ½VA + ¼VD

  35. Covariance: General Relative Pair Genetic covariance = 2VA + VD

  36. Total Genetic Variance • Heritability is the combined effect of all loci • total component = sum of individual loci components VA = VA1 + VA2 + … + VAN VD = VD1 + VD2 + … + VDN • Correlations MZ DZ P-O U • VA (2) 1 0.5 0.5 0 • VD () 1 0.25 0 0

  37. Environmental components • Shared (C) • Correlation = 1 • Nonshared (E) • Correlation = 0

  38. ACE Model for twin data 1 [0.5/1] E C A A C E e c a a c e PT1 PT2

  39. Implied covariance matrices

  40. Decomposing variance E Covariance A C 0 Adoptive Siblings 0.5 1 DZ MZ

  41. QTL Mapping Heritability analysis: Relates genome-wide average IBD sharing to phenotypic similarity QTL analysis: Relates locus-specific IBD sharing to phenotypic similarity

  42. No linkage

  43. Under linkage

  44. Path Diagram for QTL model 1 [0 / 0.5 / 1] N S Q Q S N n s q q s n PT1 PT2

  45. Exercise Write down to covariance matrices implied by the QTL path model, for sib pairs sharing 0, 1 and 2 alleles IBD.

  46. Components of variance Phenotypic Variance Environmental Genetic GxE interaction and correlation

  47. Components of variance Phenotypic Variance Environmental Genetic GxE interaction Additive Dominance Epistasis and correlation

  48. Components of variance Phenotypic Variance Environmental Genetic GxE interaction Additive Dominance Epistasis Quantitative trait loci and correlation

More Related