Question

In: Biology

Exercise 6.2 worksheet - MONOHYBRID PRACTICE PROBLEMS 1. Cystic fibrosis is an autosomal recessive genetic disorder....

Exercise 6.2 worksheet - MONOHYBRID PRACTICE PROBLEMS

1. Cystic fibrosis is an autosomal recessive genetic disorder. Ron is homozygous dominant (FF) and Nancy is a carrier (Ff ) of cystic fibrosis. Use a Punnett square to predict the genotypic and phenotypic ratios of their offspring who are normal, normal carriers, and affected. Show all your work.

Assign symbols for each allele.

Parents (P): Male ♂ =

Female ♀ =

Key

Punnett Square:

First Generation (F1)

Genotypic Ratio:

Phenotypic Ratio:

2. Patty is homozygous dominant for freckles (SS), while Charlie is homozygous for no freckles (ss). Draw a Punnett square and predict the probability that their children will have freckles.

Assign symbols for each allele.

Parents (P): Male ♂ =

Female ♀ =

Key

Punnett Square:

First Generation (F1)

Genotypic Ratio:

Phenotypic Ratio:

Probability a child will have freckles:

3. Larry and Lola Little have achondroplasia, a form of dwarfism. Both are heterozygotes. Their son, Big Bob Little, is 7'1''. (Achondroplasia is autosomal dominant, and homozygous dominant babies usually are stillborn or die shortly after birth.) Use a Punnett square to show how Big Bob got his genotype.

Assign symbols for each allele.

Big Bob Little’s Genotype =

Parents (P): Male ♂ =

Female ♀ =

Key

Punnett Square:

First Generation (F1)

Genotypic Ratio:

Phenotypic Ratio:

4. Woody Guthrie, who wrote “This Land is Your Land,” was heterozygous for Huntington’s disease (Hh). His wife was homozygous recessive and perfectly normal (hh). Huntington’s disease is caused by a latent dominant gene, meaning that it is not phenotypically (physically) expressed until later in life. Dominant disease genes are expressed in homozygous dominant and heterozygous people (HH or Hh). Draw a Punnett square for Woody and his wife and predict what percentage of their children will develop Huntington’s. Assign symbols for each allele.

Parents (P): Male ♂ =

Female ♀ =

Key

Punnett Square:

First Generation (F1)

Genotypic Ratio:

Phenotypic Ratio:

Percentage of children that will have Huntington’s disease:

Solutions

Expert Solution

1. Parents, Male ♂ = FF and Female ♀ = Ff (male first column, blue and female first row, pink)

F   f  
F   FF   Ff
F   FF   Ff

First Generation (F1)

Genotypic Ratio: 1:1, FF : Ff

Phenotypic Ratio:1:1 Normal : Carrier

Half normal children and half carriers

2. Parents, Male ♂ = ss and Female ♀ = SS (male first column, blue and female first row, pink)

S   S  
s   Ss Ss
s   Ss Ss

First Generation (F1)

Genotypic Ratio: 1, Ss

Phenotypic Ratio: 1, Freckles

All children will have freckles. Probability 100% (or probability 1)

3. Big Bob Little’s Genotype = dd

Parents, Male ♂ = Dd and Female ♀ = Dd (male first column, blue and female first row, pink)

D   d  
D   DD Dd
d   Dd dd

First Generation (F1)

Genotypic Ratio: 1:2:1, DD:Dd:dd

Phenotypic Ratio: 1:2:1, stillborn: Dwarf : Normal

So both parents were heterozygotes (Dd) and since achondroplasia is autosomal dominant, both of them were dwarfs. But their child is dd, a homozygous recessive and therefore, normal.

4. Parents, Male ♂ = Hh and Female ♀ = hh (male first column, blue and female first row, pink)

h   h  
H   Hh Hh
h   hh hh

First Generation (F1)

Genotypic Ratio: 1:1, Hh : hh

Phenotypic Ratio: 1:1, Huntington’s disease : normal

Percentage of children that will have Huntington’s disease: 50%


Related Solutions

Cystic fibrosis is an autosomal recessive genetic disorder resulting from the absence of a functional transmembrane...
Cystic fibrosis is an autosomal recessive genetic disorder resulting from the absence of a functional transmembrane conductance regulator (CFTR) protein. A woman whose older sister has a son with the disorder is concerned that she will also have a child with cystic fibrosis. The woman’s husband is healthy but he had a paternal uncle who died of cystic fibrosis as a teenager.    A. ​Based on the information given above, draw a pedigree for the couple and the extended families...
1)Cystic fibrosis an autosomal recessive disorder caused by a single gene, affects the lungs, the pancreas,...
1)Cystic fibrosis an autosomal recessive disorder caused by a single gene, affects the lungs, the pancreas, the digestive system, and other organs, resulting in symptoms ranging from breathing difficulties to recurrent infections. Which of the following terms best describes this? A)incomplete dominance B)multiple alleles C)codominance D)epistasis E)pleiotropy 2)What is one function of a signal peptide during peptide translation? A)to terminate translation of the messenger RNA B)to signal the initiation of transcription C)to bind RNA polymerase to DNA and initiate transcription...
Cystic fibrosis is an autosomal recessive disorder (c). Consider a cross between two heterozygote parents. Using...
Cystic fibrosis is an autosomal recessive disorder (c). Consider a cross between two heterozygote parents. Using a Punnett square, demonstrate what percentage of their offspring would have the disease? What are the genotypic ratios of all the possible outcomes from this cross?
Question 15 - Cystic fibrosis is transmitted as a(n): X-linked recessive gene autosomal recessive gene autosomal...
Question 15 - Cystic fibrosis is transmitted as a(n): X-linked recessive gene autosomal recessive gene autosomal dominant gene chromosomal defect
Cystic fibrosis is an autosomal recessive disease characterized by two copies of a mutated CFTR gene....
Cystic fibrosis is an autosomal recessive disease characterized by two copies of a mutated CFTR gene. If one in 100 people in the United States have cystic fibrosis and one in 5.0505050505 people are carriers for cystic fibrosis, calculate the number of individuals that are homozygous dominant. In other words, how many people would have two copies of the normal (non-mutated) CFTR gene. Use the Hardy-Weinberg equation and explain how you determined this. 
Cystic fibrosis is a recessive disorder. If a child comes from two heterozygous parents, what is...
Cystic fibrosis is a recessive disorder. If a child comes from two heterozygous parents, what is the chance that the child will have it too? 25% 75% 50% 100%
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas,...
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. CF is inherited in an autosomal recessive manner with simple Mendelian inheritance. It is caused by the presence of mutations in the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. A normal couple intends to have children but consult a genetic counselor because the man has a sister with CF and the woman has a brother with CF....
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas,...
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. CF is inherited in an autosomal recessive manner with simple Mendelian inheritance. It is caused by the presence of mutations in the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. A normal couple intends to have children but consult a genetic counselor because the man has a sister with CF and the woman has a brother with CF....
Cystic fibrosis is a genetic disorder where mutated alleles (point or gene mutations) produce a defective...
Cystic fibrosis is a genetic disorder where mutated alleles (point or gene mutations) produce a defective transport protein that results in organs producing a sticky mucus. Discuss how an individual with cystic fibrosis would make the abnormal protein. Your answer should include all the molecules and all the processes involved in going from genotype to phenotype.
Genetic Disorder: Argininosuccinic Aciduria (use for bottom section) Mode of Inheritance: By an autosomal recessive trait...
Genetic Disorder: Argininosuccinic Aciduria (use for bottom section) Mode of Inheritance: By an autosomal recessive trait Scenario 1 Both parents are afflicted with the genetic disorder. Parent Genotypes: Parent Phenotypes: Punnett Square showing the possible offspring:    Possible Offspring Genotypes: Possible Offspring Phenotypes: Probability Offspring will be afflicted with the disorder: Explanation of the results: Scenario 2 One parent is afflicted with the genetic disorder, and the second parent does not have the disorder and is not considered a carrier. Parent...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT