Adding this Class • Both sections of this class are currently full. • A lottery will be held for any spaces that become open during the first week of class. • To participate in the lottery, put your name, phone number or email address and preferred lab section on an index card and submit it to the instructor. Name Phone or Email Lab Section: AM or PM • You will be contacted if space is available. You do not need to be present to win! • Lottery will be held on Thursday of this week. Patterns of Inheritance What patterns can be observed when traits are passed to the next generation? Use of the Garden Pea for Genetics Experiments Principles of Heredity Mendel’s Experiment with Peas Round seed x Wrinkled seed F1: All round seed coats F1 round plants x F1 round plants F2: 5474 round: 1850 wrinkled (3/4 round to 1/4 wrinkled) Principles of Heredity Mendel needed to explain 1. Why one trait seemed to disappear in the first generation. 2. Why the same trait reappeared in the second generation in one-fourth of the offspring. Principles of Heredity Mendel proposed: 1. Each trait is governed by two factors – now called genes. 2. Genes are found in alternative forms called alleles. 3. Some alleles are dominant and mask alleles that are recessive. Principles of Heredity Mendel’s Experiment with Peas Round seed RR Homozygous Dominant x Wrinkled seed rr Homozygous Recessive F1: All round seed coats Rr Heterozygous Homozygous parents can only pass one form of an allele to their offspring. R R R R Heterozygous parents can pass either of two forms of an allele to their offspring. R r R r Principles of Heredity Additional Genetic Terms Genotype: alleles carried by an individual eg. RR, Rr, rr Phenotype: physical characteristic or appearance of an individual eg. Round, wrinkled Mendel’s Principle of Genetic Segregation In the formation of gametes, the members of a pair of alleles separate (or segregate) cleanly from each other so that only one member is included in each gamete. Each gamete has an equal probability of containing either member of the allele pair. Genetic Segregation Parentals: RR x rr R R R R r r r r Rr Rr Rr F1 x F1: Rr x Rr Rr R ½R ½r r R ½R ½ r ¼ RR ¼ Rr ¼ Rr ¼ rr r Genetic Segregation Genotypic Ratio: ¼ RR + ½ Rr + ¼ rr Phenotypic Ratio: ¾ Round + ¼ Wrinkled Seven Traits used by Mendel in Genetic Studies What Is a Gene? • A gene is a segment of DNA that directs the synthesis of a specific protein. • DNA is transcribed into RNA which is translated into protein. Molecular Basis for Dominant and Recessive Alleles Dominant Allele Codes for a functional protein Recessive Allele Codes for a nonfunctional protein or prevents any protein product from forming Principles of Heredity Mendel’s Experiment with Peas Round Yellow x Wrinkled Green F1: All round yellow seed coats F1 plants x F1 plants F2: 315 round, yellow 108 round, green 101 wrinkled, yellow 32 wrinkled, green 9/16 3/16 3/16 1/16 Principles of Heredity Mendel needed to explain 1. Why non-parental combinations appeared in the F2 offspring. 2. Why the ratio of phenotypes in the F2 generation was 9:3:3:1. Mendel’s Principle of Independent Assortment When gametes are formed, the alleles of one gene segregate independently of the alleles of another gene producing equal proportions of all possible gamete types. Genetic Segregation + Independent Assortment Parentals: RRYY x rryy RY RY RY RY ry ry ry RY RrYy F1: 100% RrYy, round, yellow ry ry F1 x F1: RrYy x RY Ry ¼ RY rY ry ¼ Ry RrYy RY Ry ¼ rY rY ry ¼ ry 1/16 RRYY 1/16 RRYy 1/16 RrYY 1/16 RrYy ¼ RY ¼ Ry ¼ rY ¼ ry 1/16 RRYy 1/16 RRyy 1/16 RrYy 1/16 Rryy 1/16 RrYY 1/16 RrYy 1/16 rrYY 1/16 rrYy 1/16 RrYy 1/16 Rryy 1/16 rrYy 1/16 rryy F2 Genotypes and Phenotypes Phenotypes Round Yellow Round Green Wrinkled Yellow Wrinkled Green Genotypes 1/16 RRYY + 2/16 RRYy + 2/16 RrYY + 4/16 RrYy Total = 9/16 R_Y_ 1/16 RRyy+ 2/16 Rryy Total = 3/16 R_yy 1/16 rrYY+ 2/16 rrYy Total = 3/16 rrY_ 1/16 rryy Meiotic Segregation explains Independent Assortment Solving Genetics Problems 1. Convert parental phenotypes to genotypes 2. Use Punnett Square to determine genotypes of offspring 3. Convert offspring genotypes to phenotypes Using Probability in Genetic Analysis 1. Probability (P) of an event (E) occurring: P(E) = Number of ways that event E can occur Total number of possible outcomes Eg. P(Rr) from cross Rr x Rr 2 ways to get Rr genotype 4 possible outcomes P(Rr) = 2/4 = 1/2 Using Probability in Genetic Analysis 2. Addition Rule of Probability – used in an “either/or” situation P(E1 or E2) = P(E1) + P(E2) Eg. P(Rr or RR) from cross Rr x Rr 2 ways to get Rr genotype 1 way to get RR genotype 4 possible outcomes P(Rr or RR) = 2/4 + 1/4 = 3/4 Using Probability in Genetic Analysis 3. Multiplication Rule of Probability – used in an “and” situation P(E1 and E2) = P(E1) X P(E2) Eg. P(wrinkled, yellow) from cross RrYy x RrYy P(rr and Y_) = 1/4 x 3/4 = 3/16 Using Probability in Genetic Analysis 4. Conditional Probability: Calculating the probability that each individual has a particular genotype Eg. Jack and Jill do not have PKU. Each has a sibling with the disease. What is the probability that Jack and Jill will have a child with PKU? Using Probability in Genetic Analysis 4. Conditional Probability Jack is P_, Jill is P_ Parents of Jack or Jill: Pp x Pp P p P PP Pp p Pp pp X P(Pp) = 2 ways to get Pp 3 possible genotypes P(Jack is Pp) =2/3 P (Jill is Pp) = 2/3 Using Probability in Genetic Analysis 4. Conditional Probability P(child with PKU)= P(Jack is Pp) x P(Jill is Pp) x P(child is pp) = 2/3 x 2/3 x 1/4 = 1/9 P(child without PKU)= 1-1/9 = 8/9 Using Probability in Genetic Analysis To calculate probability of child without PKU, look at all possibilities for Jack and Jill. Jack Jill P_ child Probability 1/3 PP 1/3 PP 1 1/9 1/3 PP 2/3 Pp 2/3 Pp 1/3 PP 1 1 2/9 2/9 2/3 Pp 2/3 Pp 3/4 3/9 Total=8/9 Using Probability in Genetic Analysis 5. Ordered Events: use Multiplication Rule For Jack and Jill, what is the probability that the first child will have PKU, the second child will not have PKU and the third child will have PKU? P(pp) x P(P_) x P(pp) = 1/9 x 8/9 x 1/9 = 8/729 Using Probability in Genetic Analysis 6. Binomial Rule of Probability – used for unordered events P = n! (asbt) s! t! a = probability of event X (occurrence of one event) b = probability of event Y = 1-a (occurrence of alternate event) n = total s = number of times event X occurs t = number of times event Y occurs (s + t = n) Using Probability in Genetic Analysis 6. Binomial Rule of Probability ! = factorial= number multiplied by each lower number until reaching 1 5! = 5 x 4 x 3 x 2 x 1 3! = 3 x 2 x 1 = 3 x 2! 2! = 2 x 1 1! =1 0! = 1 Using Probability in Genetic Analysis 6. Binomial Rule of Probability Out of 3 children born to Jack and Jill, what is the probability that 2 will have PKU? n=3, a=1/9, s=2, b=8/9, t=1 3! (1/9)2(8/9)1= 3 x 2! (1/81) (8/9)= 24 2! 1! 2! 1! 729 Using Probability in Genetic Analysis The same result can be obtained using the multiplicative rule if all possible birth orders for families of three are considered: 1st child 2nd child 3rd child Probability PKU=1/9 No= 8/9 PKU=1/9 No=8/9 PKU=1/9 PKU=1/9 8/729 8/729 PKU=1/9 PKU=1/9 No=8/9 8/729 8/729 + 8/729 + 8/729 = 24/729 Chi-Square Goodness of Fit Test To evaluate how well data fits an expected genetic ratio 2 (observed number expected number) 2 x expected number Chi-square Test for Goodness of Fit for 9:3:3:1 Ratio Phenotype Observed Expected Number Number (Fraction x Total) O-E (O-E)2 (O-E)2 E Round, yellow 315 9/16 x 556 = 313 2 4 .0128 Round, green 108 3/16 x 556 = 104 4 16 .154 Wrinkled, yellow 101 3/16 x 556 = 104 -3 9 .087 Wrinkled, green 32 1/16 x 556 = 35 -3 9 .257 Total 556 df=degrees of freedom= number of phenotypes – 1 = 4-1=3 p value from table on page 1-17: p>.5 from table in Pierce: .975 > p >.9 Data supports hypothesis for any p>0.05 X2= .511 p X2 Sex Determination Sex Chromosomes: homologous chromosomes that differ in size and genetic composition between males and females Human Chromosome X Y Size and gene number Larger 2142 genes Smaller 326 genes Genetic Composition Multiple genes Single gene influences unrelated gender: TDF = testis to gender determining factor Sex Determination Autosome: any chromosome that is not a sex chromosome Humans have 22 pairs of autosomes and 1 pair of sex chromosomes Human Karyotype showing homologous chromosome pairs Sex Determination Female XX x Male XY ½X ½X ½X ¼ XX ¼ XX ½Y ¼ XY ¼ XY Phenotypic Ratio of Offspring ½ Female + ½ Male X-linked Genes Hemophilic Male XhY Non-hemophilic Female (father is hemophilic) x XHXh ½ XH ½ Xh ½Y ½ Xh ¼ XHXh ¼ XhXh ¼ XHY ¼ XhY Phenotypic Ratio of Offspring ¼ hemophilic males + ¼ non-hemophilic males ¼ hemophilic females + ¼ non-hemophilic females Terms Specific to Sex-linked Genes Females Homogametic: only X found in gametes Can be homozygous or heterozygous for traits on Xchromosome Males Heterogametic: either X or Y in gametes Hemizygous for traits on the X-chromosome Patterns of Inheritance • • • • • Autosomal Dominant Autosomal Recessive X-linked Dominant X-linked Recessive Y-Linked Inheritance Pedigree for Huntington’s Disease, an Autosomal Dominant Trait Pedigree for Albinism, an Autosomal Recessive Trait Pedigree for Colorblindness, an X-linked Recessive Trait