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Ch. 5 - Genetic Linkage and Mapping in Eukaryotes
Sanders - Genetic Analysis: An Integrated Approach 3rd Edition
Sanders3rd EditionGenetic Analysis: An Integrated ApproachISBN: 9780135564172Not the one you use?Change textbook
Chapter 5, Problem 13d

Researchers cross a corn plant that is pure-breeding for the dominant traits colored aleurone (C1), full kernel (Sh), and waxy endosperm (Wx) to a pure-breeding plant with the recessive traits colorless aleurone (c1), shrunken kernel (sh), and starchy (wx). The resulting F₁ plants were crossed to pure-breeding colorless, shrunken, starchy plants. Counting the kernels from about 30 ears of corn yields the following data.
Table displaying kernel phenotypes and their corresponding counts from a trihybrid cross in corn plants.
Calculate the recombination frequencies between the gene pairs.

Verified step by step guidance
1
Step 1: Identify the parental and recombinant phenotypes. Parental phenotypes are those that match the original combinations of alleles in the parents, while recombinant phenotypes result from crossing over during meiosis.
Step 2: Sum the number of parental offspring. From the table, parental genotypes are 'se cu e / se cu e' (340 individuals) and '+ + + / se cu e' (300 individuals). Add these numbers together.
Step 3: Sum the number of recombinant offspring. Recombinant genotypes are all other combinations listed in the table. Add the numbers for 'se cu + / se cu e' (60), 'se + + / se cu e' (110), '+ cu e / se cu e' (84), '+ + e / se cu e' (80), 'se + e / se cu e' (10), and '+ cu + / se cu e' (16).
Step 4: Calculate the total number of offspring by summing all the values in the table. This will be used to determine the recombination frequency.
Step 5: Compute the recombination frequency using the formula: \( \text{Recombination Frequency} = \frac{\text{Number of Recombinant Offspring}}{\text{Total Number of Offspring}} \times 100 \). This will give the percentage of recombination between the gene pairs.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Mendelian Genetics

Mendelian genetics is the study of how traits are inherited through generations based on the principles established by Gregor Mendel. It includes concepts such as dominant and recessive traits, genotype and phenotype, and the segregation and independent assortment of alleles during gamete formation. Understanding these principles is crucial for analyzing inheritance patterns in the corn plant cross described in the question.
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Descriptive Genetics

Recombination Frequency

Recombination frequency is a measure of the likelihood that two genes located on the same chromosome will be separated during meiosis due to crossing over. It is calculated by dividing the number of recombinant offspring by the total number of offspring and is expressed as a percentage. This concept is essential for determining the genetic linkage between the traits in the corn plants and understanding how closely related the genes are.
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Recombination after Single Strand Breaks

Phenotypic Ratios

Phenotypic ratios represent the relative frequencies of different phenotypes in the offspring resulting from a genetic cross. These ratios can provide insights into the inheritance patterns of traits and help in predicting the outcomes of future crosses. In the context of the corn plant experiment, analyzing the phenotypic ratios of the kernels will aid in calculating recombination frequencies and understanding the genetic relationships among the traits.
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Mutations and Phenotypes
Related Practice
Textbook Question

Researchers cross a corn plant that is pure-breeding for the dominant traits colored aleurone (C1), full kernel (Sh), and waxy endosperm (Wx) to a pure-breeding plant with the recessive traits colorless aleurone (c1), shrunken kernel (sh), and starchy (wx). The resulting F₁ plants were crossed to pure-breeding colorless, shrunken, starchy plants. Counting the kernels from about 30 ears of corn yields the following data.

Why are these data consistent with genetic linkage among the three genes?

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Textbook Question

Researchers cross a corn plant that is pure-breeding for the dominant traits colored aleurone (C1), full kernel (Sh), and waxy endosperm (Wx) to a pure-breeding plant with the recessive traits colorless aleurone (c1), shrunken kernel (sh), and starchy (wx). The resulting F₁ plants were crossed to pure-breeding colorless, shrunken, starchy plants. Counting the kernels from about 30 ears of corn yields the following data.


Perform a chi-square test to determine if these data show significant deviation from the expected phenotype distribution.

479
views
Textbook Question

Researchers cross a corn plant that is pure-breeding for the dominant traits colored aleurone (C1), full kernel (Sh), and waxy endosperm (Wx) to a pure-breeding plant with the recessive traits colorless aleurone (c1), shrunken kernel (sh), and starchy (wx). The resulting F₁ plants were crossed to pure-breeding colorless, shrunken, starchy plants. Counting the kernels from about 30 ears of corn yields the following data.

What is the order of these genes in corn?

439
views
Textbook Question

Researchers cross a corn plant that is pure-breeding for the dominant traits colored aleurone (C1), full kernel (Sh), and waxy endosperm (Wx) to a pure-breeding plant with the recessive traits colorless aleurone (c1), shrunken kernel (sh), and starchy (wx). The resulting F₁ plants were crossed to pure-breeding colorless, shrunken, starchy plants. Counting the kernels from about 30 ears of corn yields the following data.

What is the interference value for this data set?

490
views
Textbook Question

Nail–patella syndrome is an autosomal disorder affecting the shape of nails on fingers and toes as well as the structure of kneecaps. The pedigree below shows the transmission of nail–patella syndrome in a family along with ABO blood type. Is nail–patella syndrome a dominant or a recessive condition?

Is nail–patella syndrome a dominant or a recessive condition? Explain your reasoning.

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Textbook Question

Nail–patella syndrome is an autosomal disorder affecting the shape of nails on fingers and toes as well as the structure of kneecaps. The pedigree below shows the transmission of nail–patella syndrome in a family along with ABO blood type.

Does this family give evidence of genetic linkage between nail–patella syndrome and ABO blood group? Why or why not?

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