Question

In: Biology

Try-Sachs is a disease characterized by progressive neurologic degeneration, and is caused by a recessive mutation....

Try-Sachs is a disease characterized by progressive neurologic degeneration, and is caused by a recessive mutation. In a certain population, the rate of Try-Sachs is 1 in 4000 births. What is the chance of being a carrier in the population?

Name three common features of plasmid vectors and what can be accomplished by each. Indicate the features that are absolutely required and why (one clear sentence about why).   

           

  

  

Solutions

Expert Solution

Q1)

Given that:

Rate of Tay Sachs = 1 in 4000 births.

Since Tay-Sachs disease is an autosomal recessive disease, the disease is only present in homozygous recessive individuals.
Therefore, the frequency of the homozygous recessive phenotype = q2 = 1/4000 = 0.00025

Therefore, q = =

Thus, p = 1 - q = 1 - 0.0158 = 0.9842

The frequency of carriers can be calculated by Freq(carrier) = 2pq = 2 * 0.9842 * 0.0158 = 0.0311

Thus, the probability of being a carrier for Tay Sachs in this populaiton is 0.0311.

Q2)

Three features that are common for all plasmid vectors are:

  1. Origin of replication: This is a sequence that is recognized by the DNA replication machinery for the replication of the plasmid DNA molecule. This sequence is required to maintain the plasmid in successive generations.
  2. Selectable Marker (Usually antibiotic resistance): A selectable marker is required as it allows users to select for cells that carry the plasmid and not for cells that do not carry the plasmid. This is usually achieved by incorporating an antibiotic resistance gene in the plasmid and then growing the cells in antibiotic-containing media. Only cells that have the plasmid with the resistance gene are able to grow in these conditions.
  3. Multiple Cloning Site: Almost all plasmid vectors also have a Multiple Cloning Site (MCS) that allows users to clone desired DNA fragments into the vector eitehr for expression or for preparing a library.

Related Solutions

Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by...
Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by a build-up of mucus in the lungs and difficulty breathing. A woman whose maternal uncle had the disease is trying to determine the probability she and her husband could have an affected child. Her husband's sister died of the disease. Assuming the uncle and the sister are the only family members who had the disease, what is the chance that the couple's first child...
Tay-Sachs disease is inherited as an autosomal recessive trait and is lethal in the homozygous recessive...
Tay-Sachs disease is inherited as an autosomal recessive trait and is lethal in the homozygous recessive condition at the age of 2years. A heterozygote marries a genotypically normal individual. What is the probability of having children that have Tay-Sachs?
Tay-Sachs is an autosomal recessive disorder that results in progressive loss of brain tissue Jewish settlers...
Tay-Sachs is an autosomal recessive disorder that results in progressive loss of brain tissue Jewish settlers and is engaged to Howard. Maria and Howard are concerned about having children since one of Maria’s uncles on her mother’s side had died from Tay Sachs. Howard’s family is of Scandinavian origin has no record of Tay Sach. You are asked to advise Maria and Howard as to the risk of them having a child with Tay Sachs. (FYI, the incidence of Tay...
Sickle cell anemia is a recessive disorder caused by a mutation in the hemoglobin A gene....
Sickle cell anemia is a recessive disorder caused by a mutation in the hemoglobin A gene. Persons with the disease have a variety of serious health issues related to fragile and sickling red blood cells including premature death, and infants sometimes die from complications. In regions of central Africa where malaria is endemic, the relative fitnesses for individuals that are homozygous for the wild type hemoglobin allele (HbA), heterozygous (HbAHbS), and homozygous for the sickle cell allele (HbS) are 0.8,...
Cystic fibrosis is caused by a mutation in a single gene. Homozygotes for this mutant recessive...
Cystic fibrosis is caused by a mutation in a single gene. Homozygotes for this mutant recessive allele (ff) have cystic fibrosis. Within a population, 2% of people have cystic fibrosis. Assuming Hardy-Weinberg equilibrium, the frequency of heterozygotes in the population is 0.24. If inbreeding was common in this population, what would happen to the percentage of people who have cystic fibrosis over time?
Fill in the blank. Duchenne muscular dystrophy is caused by an X-linked recessive mutation in the...
Fill in the blank. Duchenne muscular dystrophy is caused by an X-linked recessive mutation in the DMD gene, which encodes the protein dystrophin. A female without the disease mates with a male with Duchenne muscular dystrophy; they have two sons and two daughters. The first son has the disease as does their first daughter. Based on this, the probability that the second son will have the disease is________________ The probability that the second daughter will be a carrier is____________
Another disease caused by a mutation in a single gene is Huntington’s disease (HD), an autosomal...
Another disease caused by a mutation in a single gene is Huntington’s disease (HD), an autosomal dominant condition. It is caused by mutations in a gene required for normal nerve cell function. The mutations cause abnormal proteins to be produced which “stick” together and accumulate in nerve cells, eventually interfering with normal cell operations. Suggest two ways you could treat the disease by targeting the translation step for the HD protein and justify why each approach might be effective.
Hemophilia is a disease caused by a recessive allele on the X chromosome. Use a Punnett...
Hemophilia is a disease caused by a recessive allele on the X chromosome. Use a Punnett square to help describe the offspring phenotypes from the cross: heterozygous female crossed to male with hemophilia.
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. 
Assuming Hardy-Weinberg conditions are met: a rare disorder is caused by an autosomal recessive mutation. Calculate...
Assuming Hardy-Weinberg conditions are met: a rare disorder is caused by an autosomal recessive mutation. Calculate the percentage of heterozygous carriers in a population if the disease affects 1 in 15,000 individuals (show your work).
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT