Question

6.Tay-Sachs disease is an autosomal recessive disorder that causes degeneration of nerve tissue in infants. Infants...

6.Tay-Sachs disease is an autosomal recessive disorder that causes degeneration of nerve tissue in infants. Infants with Tay-Sachs disease develop blindness, paralysis, and die at an early age. The gene for this disorder is located on chromosome 15. Sickle cell anemia is another autosomal recessive disorder. A person who is homozygous recessive for the sickle cell allele will have an abnormal hemoglobin protein which causes the red blood cells to have a sickle shape. The misshapen blood cells block capillaries which restricts blood flow. This gene is located on chromosome 11. A woman finds out she is heterozygous or a carrier of recessive alleles for both genetic disorders. Using your understanding of the laws of segregation and independent assortment, explain how meiosis leads to only a 25% chance of any of her eggs having both recessive alleles. (If you are trying to answer this question using a Punnett square, you are incorrect. A Punnett square simulates fertilization which assumes that meiosis and egg or sperm have already been produced.)

0 0
Add a comment Improve this question Transcribed image text
Answer #1

Answer:

Law of Independent Assortment:

                        It states that factors (genes) for different pairs of contrasting characters are assorted independent of one another during gamete formation. This implies that during gamete formation, the alleles for sickle cell disease do not interfere with alleles for Tay0sacgas disease and the two pairs of alleles behave independent of each other.

Tay-sachs gene has two alleles, T & t. Each allele has equal chance (50%) of getting inherited.

Sickle cell anemia has two alleles, S & s. Each allele has equal chance (50%) of getting inherited.

TtSs genotype produces 4 types of gametes, the probability of each gamete is as follows:

TS = 50% * 50% = 25%

Ts = 50% * 50% = 25%

tS = 50% * 50% = 25%

ts = 50% * 50% = 25%

Add a comment
Know the answer?
Add Answer to:
6.Tay-Sachs disease is an autosomal recessive disorder that causes degeneration of nerve tissue in infants. Infants...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Tay-Sachs Disease is an autosomal recessive disease. That means that it is carried on one of...

    Tay-Sachs Disease is an autosomal recessive disease. That means that it is carried on one of the autosomal chromosomes and that only individuals with the two recessive disease alleles will have the disease phenotype. John and Sue are both carriers of the disease. Use the letters T and t to represent alleles. a.) What is John’s genotype? b.)Sue’s genotype? c.) What percentage of their children would you predict to have Tay-Sachs Disease? Show your work with a Punnett square.

  • 2) Tay-Sachs disease is an autosomal recessive neurological disorder that is fatal in infancy. Despite its...

    2) Tay-Sachs disease is an autosomal recessive neurological disorder that is fatal in infancy. Despite its invariably lethal effect, Tay-Sachs disease occurs at very high frequency in some Central and Eastern European (Ashkenazi) Jewish populations. In certain Ashkenazi populations, 1 in 1000 infants has Tay-Sachs disease. Population biologists believe the high frequency is a consequence of genetic bottlenecks caused by pogroms (genocide) that have reduced the population multiple times in the last several hundred years. a) In the population described,...

  • BATO manner. This diseaSe is inherited in an autosomal recessive (15 pts) Tay-Sachs disease is a...

    BATO manner. This diseaSe is inherited in an autosomal recessive (15 pts) Tay-Sachs disease is a mutation in the HEXA gene, resulting in low EXA gene, resulting in low level of the enzyme hexosaminidase A. Tay-Sachs abilities and results in death by the disease causes deterioration of mental and physical age of four. e in which a family member (shaded) died from Tay-Sachs disease. n she had a blood finds that she is a carrier for Tay-Sachs disease whe Individual...

  • Tay-Sachs disease is an autosomal recessive disorder. Among Ashkenazi Jews of central European ancestry about in...

    Tay-Sachs disease is an autosomal recessive disorder. Among Ashkenazi Jews of central European ancestry about in 1/3600 children are born with Tay-Sachs disease. What is the frequency for being a carrier for Tay-Sachs in this population? A carrier does not show the trait but can pass it on to his/her offspring.

  • Infantile Tay-Sachs disease is a neurological disorder that causes a progressive deterioration of nerve cells resulting...

    Infantile Tay-Sachs disease is a neurological disorder that causes a progressive deterioration of nerve cells resulting in seriously impaired mental and physical abilities. It usually results in death by the age of four. Infantile Tay-Sachs is a recessive disorder (aa) affecting 1 in 3000 individuals. (show your work) (10pts) a) What is the frequency of the "aa" genotype in this population? b) What is the frequency of the "q" allele? c) What is the frequency of the "p" allele? d)...

  • Tay-Sachs disease is an autosomal recessive disorder caused by a mutation in the HEXA gene that...

    Tay-Sachs disease is an autosomal recessive disorder caused by a mutation in the HEXA gene that results in progressive deterioration of the nervous system. Affected indivisuals usually die by age 4. Let D represent the wildtype allele and d the disease-causing allele. Because the Tay-Sachs disease allele has been observed at relatively high frequencies in several human populations, it has ocassionally been suggested that this locus may be subject to balancing selection due to heterozygote advantage. Here we will explore...

  • 1. Tay-Sachs is an autosomal recessive disorder, which is the inability for infants to breakdown gangliosides in the CNS, which overtime build-up and destroy neurons. As the disease progresses, the ch...

    1. Tay-Sachs is an autosomal recessive disorder, which is the inability for infants to breakdown gangliosides in the CNS, which overtime build-up and destroy neurons. As the disease progresses, the child loses muscle control. Eventually, this leads to blindness, paralysis and death. If you have a family history of Tay-Sachs disease or if you're a member of a high-risk group and plan to have children, doctors strongly recommend genetic testing and genetic counseling. Scott and Tina are a young couple...

  • Please provide answers with explanations for these questions. 1. Tay Sachs disease is an inherited disorder....

    Please provide answers with explanations for these questions. 1. Tay Sachs disease is an inherited disorder. Children who are born with Tay Sachs have progressive neurological problems and typically die before age 4. It is inherited in an autosomal recessive manner Below are pedigrees from two families where some members of a family have Tay Sachs disease. Neither Hillary nor Justin have Tay Sachs disease. If Hillary and Justin have a child, what is the chance this child will have...

  • 3. Sickle-cell disease is a genetic condition caused by an autosomal recessive allele which al- fects...

    3. Sickle-cell disease is a genetic condition caused by an autosomal recessive allele which al- fects one in every 500 African American children born in the U.S. One in every ten African Americans is a carrier for the recessive allels. Although sickle cell disease is caused by a single human gene, it is expressed through many different effects throughout the body. The presence of a recessive sickle-cell allele in humans causes the red blood cells to produce abnormal hemoglobin protein...

  • Use the information presented below to answer questions 6 - 8. Tay-Sachs disease is a recessive...

    Use the information presented below to answer questions 6 - 8. Tay-Sachs disease is a recessive hereditary abnormality causing death within the first few years of life in individuals with the genotype tt. These individuals never reach sexual maturity. Individuals with the genotype T do not become diseased. Abnormally shortened fingers (brachyphalangy) are due to the presence of alleles in the heterozygous condition (Bb) located at a different locus. Geneticists observed that brachyphalangy was conveyed by the dominant allele and...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT