Podcast
Questions and Answers
What phenotype corresponds to the genotype b+ vg+ pr+?
What phenotype corresponds to the genotype b+ vg+ pr+?
Which of the following phenotypes represents the genotype b vg+ pr?
Which of the following phenotypes represents the genotype b vg+ pr?
What effect do double crossovers have on genetic mapping?
What effect do double crossovers have on genetic mapping?
What is the total number of testcross progeny observed?
What is the total number of testcross progeny observed?
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Which phenotype has the highest count in the testcross progeny?
Which phenotype has the highest count in the testcross progeny?
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When is it necessary to perform a c2 goodness of fit test?
When is it necessary to perform a c2 goodness of fit test?
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Why are full genetic maps difficult to construct in humans?
Why are full genetic maps difficult to construct in humans?
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What is the effect of the third gene on the progeny phenotype determination?
What is the effect of the third gene on the progeny phenotype determination?
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Which statement highlights the reality of crossover events?
Which statement highlights the reality of crossover events?
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What is a primary challenge in assessing recombination frequencies for genes that are far apart?
What is a primary challenge in assessing recombination frequencies for genes that are far apart?
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What is the primary purpose of a testcross in the context of linked genes?
What is the primary purpose of a testcross in the context of linked genes?
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During the testcross, which phenotypes were produced in the F1 generation?
During the testcross, which phenotypes were produced in the F1 generation?
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Which of the following phenotypic proportions was recorded from the testcross outcomes?
Which of the following phenotypic proportions was recorded from the testcross outcomes?
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How does the discovery of linkage influence our understanding of genetic inheritance?
How does the discovery of linkage influence our understanding of genetic inheritance?
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What combinations represent linked genes in the given testcross?
What combinations represent linked genes in the given testcross?
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What is the percentage of recombinants identified for the first trait combination?
What is the percentage of recombinants identified for the first trait combination?
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Which trait combination contributes the highest number of parental types?
Which trait combination contributes the highest number of parental types?
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What is the total number of offspring observed in the experiment?
What is the total number of offspring observed in the experiment?
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How many total recombinants were calculated for the black body and vestigial wing combination?
How many total recombinants were calculated for the black body and vestigial wing combination?
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Which trait combination shows a total of 60 offspring with black body and wild type eyes?
Which trait combination shows a total of 60 offspring with black body and wild type eyes?
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What percentage corresponds to the total recombinants seen for the combination of purple eye and vestigial wing?
What percentage corresponds to the total recombinants seen for the combination of purple eye and vestigial wing?
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Which of the following combinations had the least number of recorded offspring?
Which of the following combinations had the least number of recorded offspring?
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What is the correct recombinant calculation for the trait combination of purple eye and vestigial wing?
What is the correct recombinant calculation for the trait combination of purple eye and vestigial wing?
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What is the recombination frequency (RF) between loci b and vg?
What is the recombination frequency (RF) between loci b and vg?
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What does a coefficient of coincidence (C) of 0.4 indicate in this context?
What does a coefficient of coincidence (C) of 0.4 indicate in this context?
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How do you calculate the expected number of double crossovers (DCO) among 1005 offspring?
How do you calculate the expected number of double crossovers (DCO) among 1005 offspring?
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What impact do double crossovers have on the parental arrangement of loci?
What impact do double crossovers have on the parental arrangement of loci?
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When calculating true recombination frequency, how are double recombinants factored in?
When calculating true recombination frequency, how are double recombinants factored in?
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What is the chance of double crossover occurring between loci b and vg based on their recombination frequencies?
What is the chance of double crossover occurring between loci b and vg based on their recombination frequencies?
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What does the calculated distance of 18.4 mu represent?
What does the calculated distance of 18.4 mu represent?
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What does the presence of fewer double crossovers than expected suggest about the genetic loci?
What does the presence of fewer double crossovers than expected suggest about the genetic loci?
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Study Notes
Linkage and Testcrosses
- Linkage is examined through testcrosses, which reveal the relationship between genes.
- Example cross: P1 (pr+ pr+; vg+ vg+) and P2 (pr pr; vg vg) produce wild type and purple, vestigial phenotypes.
- The testcross of F1 generation pr+ pr; vg+ vg with pr pr; vg vg yields specific gametes.
Phenotype Proportions
- Observed phenotypes from testcross:
- Wild type: 1339
- Vestigial: 154
- Purple: 151
- Purple, vestigial: 1195
- Total offspring: 2839
- Recombinant frequencies (RF) indicate linkage between genes, with specific RF values:
- pr and vg: RF = 37.5%, map distance = 57.6 mu
- w and m: RF = 45.2%, map distance = 56.6 mu
Double Crossovers
- Double crossovers can obscure mapping, reverting genes to parental arrangements and complicating interpretations.
- The likelihood of double crossovers increases with distance between gene loci.
Testing Gene Linkage
- High RF (>25%) may suggest that genes are linked; confirm through chi-square goodness of fit testing.
- Supporting the null hypothesis indicates chance variation, supporting unlinking of genes.
- Rejecting the null suggests variation resulting from linkage.
Genetic Mapping Challenges
- Genetic maps often utilize intermediate genes due to inaccuracies in mapping far-apart genes.
- Mapping in humans is difficult due to limited progeny, inability to perform desired crosses, and reliance on pedigree analysis.
Assumptions in Genetic Mapping
- Crossovers are typically assumed to occur only between non-sister chromatids for simplicity.
- Reality includes potential double crossovers among four chromatids.
Mapping with Trihybrid Test Crosses
- Possible female gametes illustrate genetic combinations.
- All testcross male gametes yield the same genotype (b vg pr).
- Progeny phenotype proportions provide data for mapping distances.
Calculating Map Distances
- Analyze pairs of genes to calculate recombination frequencies.
- Example calculations yield:
- Black body and purple eye recombinants: 6.1%
- Black body and vestigial wing: 17.8%
- Purple eye and vestigial wing: 12.3%
Influence of Double Crossovers
- Double crossovers between outer loci appear as parental combinations but modify frequencies for the inner locus.
- Adjust calculations for true RF by including double recombinants.
Interference and Coefficient of Coincidence
- Interference assesses whether one crossover affects the occurrence of another nearby.
- Expected double crossovers calculated using map distances.
- Coefficient of coincidence (C) indicates the relationship between observed and expected double crossovers, calculated as:
- C = Observed DCO / Expected DCO, providing insight into crossover interactions.
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Description
This quiz explores the concept of genetic linkage through testcrosses, specifically focusing on the linkage of the pr and vg genes. It examines the results of crossing wild type and mutant phenotypes, providing insights into the inheritance patterns of linked genes.