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Genetics: Calculating Map Units and Frequencies of Genotypes and Phenotypes in Crosses, Summaries of Genetics

Information on calculating map units and frequencies of genotypes and phenotypes in genetic crosses. It includes examples of crosses with different genotypes and the resulting frequencies of parental and recombinant types. The document also explains the concept of linkage and how it affects the frequency of recombination between genes.

Typology: Summaries

2021/2022

Uploaded on 09/12/2022

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Download Genetics: Calculating Map Units and Frequencies of Genotypes and Phenotypes in Crosses and more Summaries Genetics in PDF only on Docsity! 1. You perform the following cross and are told that the two genes are 10 m.u. apart. A B/a b × a b/a b Among their progeny, 10 percent should be recombinant (A b/a b and a B/a b) and 90 percent should be parental (A B/a b and a b/a b). Therefore, A B/a b should represent 1/2 of the parentals or 45 percent. 2. P A d / A d × a D / a D F1 A d / a D F2 1 A d / A d phenotype: A d 2 A d / a D phenotype: A D 1 a D / a D phenotype: a D 3. P R S/r s × R S/r s gametes 1/2 (1 – 0.35) R S 1/2 (1 – 0.35) r s 1/2 (0.35) R s 1/2 (0.35) r S F1 genotypes 0.1056 R S/R S 0.1138 r s/r S 0.1056 r s/r s 0.1138 r s/R s 0.2113 R S/r s 0.0306 R s/R s 0.1138 R S/r S 0.0306 r S/r S 0.1138 R S/R s 0.0613 R s/r S F1 phenotypes 0.6058 R S 0.1056 r s 0.1444 R s 0.1444 r S 5. Because only parental types are recovered, the two genes must be tightly linked and recombination must be very rare. Knowing how many progeny were looked at would give an indication of how close the genes are. 6. The problem states that a female that is A/a · B/b is test crossed. If the genes are unlinked, they should assort independently and the four progeny classes should be present in roughly equal proportions. This is clearly not the case. The A/a · B/b and a/a · b/b classes (the parentals) are much more common than the A/a · b/b and a/a · B/b classes (the recombinants). The two genes are on the same chromosome and are 10 map units apart. RF = 100% × (46 + 54)/1000 = 10% A B a b 10 m.u. 56 Chapter Four 7. The cross is A/A · B/B × a/a · b/b. The F1 would be A/a · B/b. a. If the genes are unlinked, all four progeny classes from the test cross (including a/a ; b/b) would equal 25 percent. b. With completely linked genes, the F1 would produce only A B and a b gametes. Thus, there would be a 50 percent chance of having a b/a b progeny from a test cross of this F1. c. If the two genes are linked and 10 map units apart, 10 percent of the test cross progeny should be recombinants. Since the F1 is A B/a b, a b is one of the parental classes (A B being the other) and should equal 1/2 of the total non-recombinants or 45 percent. d. 38 percent (see part c) 8. Meiosis is occurring in an organism that is C d/c D, ultimately producing haploid spores. The parental genotypes are C d and c D, in equal frequency. The recombinant types are C D and c d, in equal frequency. Eight map units means 8 percent recombinants. Thus, C D and c d will each be present at a frequency of 4 percent, and C d and c D will each be present at a frequency of (100% – 8%)/2 = 46%. a. 4 percent b. 4 percent c. 46 percent d. 8 percent 10. a. The three genes are linked. b. Comparing the parentals (most frequent) with the double crossovers (least frequent), the gene order is v p b. There were 2200 recombinants between v and p, and 1500 between p and b. The general formula for map units is m.u. = 100%(number of recombinants)/total number of progeny Therefore, the map units between v and p = 100%(2200)/10,000 = 22 m.u., and the map units between p and b = 100%(1500)/10,000 = 15 m.u. The map is c. I = 1 – observed double crossovers/expected double crossovers = 1 – 132/(0.22)(0.15)(10,000) = 1 – 0.4 = 0.6 11. P a b c/a b c × a+ b+ c+/a+ b+ c+ F1 a+ b+ c+/a b c × a+ b+ c+/a b c Chapter Four 59 c. Because both genes are X-linked, this represents crossing-over. The progeny size is too small to give a reliable estimate of recombination. 22. a. If the genes are unlinked, the cross becomes P hyg/hyg ; her/her × hyg+/hyg+ ; her+/her+ F1 hyg+/hyg ; her+/her × hyg+/hyg ; her+/her F2 9/16 hyg+/– ; her+/– 3/16 hyg+/– ; her/her 3/16 hyg/hyg ; her+/– 1/16 hyg/hyg ; her/her So only 1/16 (or 6.25 percent) of the seeds would be expected to germinate. b. and c. No. More than twice the expected seeds germinated so assume the genes are linked. The cross then becomes P hyg her/hyg her × hyg+ her+/hyg+ her+ F1 hyg+ her+/hyg her × hyg+ her+/hyg her F2 13 percent hyg her/hyg her Because this class represents the combination of two parental chromosomes, it is equal to p(hyg her) × p(hyg her) = (1/2 parentals)2 = 0.13 and parentals = 0.72 so recombinants = 1 – 0.72 = 0.28 Therefore, a test cross of hyg+ her+/hyg her should give 36% hyg+ her+/hyg her 36% hyg her/hyg her 14% hyg+ her/hyg her 14% hyg her+/hyg her and 36 percent of the progeny should grow (the hyg her/hyg her class). 28. a. The cross is A · arg-1 × a · arg-1+. Use the classification of asci in part (17) above. First decide if the two genes are linked by using the formula PD>>NPD, when the genes are linked, while PD = NPD when they are not linked. PD = 127 + 2 = 129 and NPD = 125 + 4 = 129, which means that the two genes are not linked. Alternatively, RF = 100%(1/2 T + NPD)/total asci 60 Chapter Four = 100%[(1/2)(100 + 36 + 6) + (125 + 4)]/400 = 50%. Next calculate the distance between each gene and its centromere using the formula RF = 100%(1/2 number of tetrads exhibiting MII segregation)/(total number of asci). A–centromere = 100%(1/2)(36 + 2 + 4 + 6)/400 = 100%(24/400) = 6 m.u. arg+–centromere = 100%(1/2)(100 + 2 + 4 + 6)/400 = 100%(56/400) = 14 m.u. b. Class 6 can be obtained if a single crossover occurred between chromatids 2 and 3 between each gene and its centromere. 29. Before beginning this problem, classify all asci as PD, NPD, or T and determine whether there is MI or MII segregation for each gene: Asci type 1 2 3 4 5 6 7 type PD NPD T T PD NPD T gene a I I I II II II II gene b I I II I II II II If PD >> NPD, linkage is indicated. The distance between a gene and its centromere = 100% (1/2)(MII)/total. The distance between two genes = 100% (1/2T + NPD)/total. Cross 1: PD = NPD and RF = 50%; the genes are not linked. Chapter Four 61 a–centromere: 100% (1/2)(0)/100 = 0 m.u. Gene a is close to the centromere. b–centromere: 100% (1/2)(32)/100 = 16 m.u. Cross 2: PD >> NPD; the genes are linked. a–b: 100% [1/2(15) + 1]/100 = 8.5 m.u. a–centromere: 100% (1/2)(0)/100 = 0 m.u. Gene a is close to the centromere. b–centromere: 100% (1/2)(15)/100 = 7.5 m.u. Cross 3: PD >> NPD; the genes are linked. a–b: 100% [1/2(40) + 3]/100 = 23 m.u. a–centromere: 100% (1/2)(2)/100 = 1 m.u. b–centromere: 100% (1/2)(40 + 2)/100 = 21 m.u. Cross 4: PD > > NPD; the genes are linked. a–b: 100% [1/2(20) + 1]/100 = 11 m.u. a–centromere: 100% (1/2)(10)/100 = 5 m.u. b–centromere: 100% (1/2)(18 + 8 + 1)/100 = 13.5 m.u. Cross 5: PD = NPD (and RF = 49%); the genes are not linked. a–centromere: 100% (1/2)(22 + 8 + 10 + 20)/99 = 30.3 m.u. b–centromere: 100% (1/2)(24 + 8 + 10 + 20)/99 = 31.3 m.u. These values are approaching the 67 percent theoretical limit of loci exhibiting MII patterns of segregation and should be considered cautiously. Cross 6: PD >> NPD; the genes are linked. a–b: 100% [1/2(1 + 3 + 4) + 0]/100 = 4 m.u. a–centromere: 100% (1/2)(3 + 61 + 4)/100 = 34 m.u. b–centromere: 100% (1/2)(1 + 61 + 4)/100 = 33 m.u. These values are at the 67 percent theoretical limit of loci exhibiting MII patterns of segregation and therefore both loci can be considered unlinked to the centromere. Cross 7: PD >> NPD; the genes are linked. a–b: 100% [1/2(3 + 2) + 0]/100 = 2.5 m.u. a–centromere: 100% (1/2)(2)/100 = 1 m.u. b–centromere: 100% (1/2)(3)/100 = 1.5 m.u. Cross 8: PD = NPD; the genes are not linked. a–centromere: 100% (1/2)(22 + 12 + 11+ 22)/100 = 33.5 m.u. b–centromere: 100% (1/2)(20 + 12 + 11 + 22)/100 = 32.5 m.u. Same as cross 5. Cross 9: PD >> NPD; the genes are linked. a–b: 100% [1/2(10 + 18 + 2) + 1]/100 = 16 m.u. a–centromere: 100% (1/2)(18 + 1 + 2)/100.= 10.5 m.u. 64 Chapter Four A B c 30 a b C 30 c. Interference = 1 – observed DCO/expected DCO 0.2 = 1 – observed DCO/(0.20)(0.30) observed DCO = (0.20)(0.30) – (0.20)(0.20)(0.30) = 0.048 The A–B distance = 20% = 100% [p(CO A–B) + p(DCO)]. Therefore, p(CO A–B) = 0.20 – 0.048 = 0.152 Similarly, the B–C distance = 30% = 100% [p(CO B–C) + p(DCO)] Therefore, p(CO B–C) = 0.30 – 0.048 = 0.252 The p(parental) = 1 – p(CO A–B) – p(CO B–C) – p(observed DCO) = 1 – 0.152 – 0.252 – 0.048 = 0.548 So for 1,000 progeny, the expected results are A b c 274 a B C 274 A B C 76 a b c 76 A b C 126 a B c 126 A B c 24 a b C 24 42. Crossing-over occurs 8 percent of the time between w and s, which means it does not occur 92 percent of the time. Crossing-over occurs 14 percent of the time between s and e, which means that it does not occur 86 percent of the time. a. and b. The frequency of parentals = p (no crossover between either gene) = p(no CO w–s) × p(no CO s–e) = (0.92)(0.86) = 0.791 or 1/2(0.791) = 0.396 each c. and d. The frequency that will show recombination between w and s only = p(CO w–s) × p(no CO s–e) = (0.08)(0.86) = 0.069 or 1/2(0.069) = 0.035 each e. and f. The frequency that will show recombination between s and e only = p(CO s–e) × p(no CO w–s) = (0.14)(0.92) = 0.128 or 1/2(0.128) = 0.064 each g. and h. The frequency that will show recombination between w and s and s and e Chapter Four 65 = p(CO w–s) × p(CO s–e) = (0.08)(0.14) = 0.011 or 1/2(0.011) = 0.006 each
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