describe why X chromosome polyploidy is tolerated in humans while polyploidy in other chromosome is not tolerated? use the example of trisomy 21 to explain why polyploidy is damaging to the normal functionality of the cell.
X-chromosome polyploidy is tolerated
in humans due to the X-inactivation mechanism
i.e. if a person contains more than one X-chromosome, they will get
inactivated by an epigenetic mechanism.
It is a random process that leaves only one functional X-chromosome
in the cell.
The inactivated X-chromosome = Barr body
Ex: XX = 1 Barr body
XY = 0 Barr body
XXY = 1 Barr body
XXX = 2 Barr bodies
However, excess copies of autosomes do not get inactivated. As a
result, elevated levels of gene products are produced leading to
abnormal phenotypes.
Hence, X-chromosome polyploidy is tolerated than autosomal
polyploidy.
describe why X chromosome polyploidy is tolerated in humans while polyploidy in other chromosome is not...
1. In humans, X and Y chromosomes are technically not homolous Explain how X and Y chromosomes pair up in cells of males prior to cell division 2. Familial breast cancer is caused by mutations in the BRCA1 gene which is located on human chromosome 17. Females with a mutation in BRCA1 gene have an 80% lifetime risk of developing breast cancer. Therefore, out of 100 women who carry the disease-causing mutation, only 80 will develop breast cancer. Why is...
Given that TP53 is a recessive gene and is not located on the X chromosome, why would people who inherit just one mutant copy of a recessive tumor-suppressor gene be at higher risk of developing cancer than those without the recessive gene? Given that is a recessive gene and is not located on the X chromosome, why would people who inherit just one mutant copy of a recessive tumor-suppressor gene be at higher risk of developing cancer than those without...
84. Each version of a gene is called a(n) a. allele. b. chromosome. c. histone. d. centromere. e. artifact. Matching: Choose the one most appropriate condtion from a - e for each of the descriptions below for numbers 85-89. Each answer is only used once a. Down's syndrome b. Huntington's disease or Huntington's chorea c. hemophilia d. Turner syndrome e. sickle cell anemia 85. Dominant deadly disease that occurs after the age of 30, affects nerves and movement 86. nondisjunction...
2. Explain why the replication of one of the DNA strands is continuous while the other strand is discontinuous. What causes this difference? 3. A) What are telomeres? B) Are telomeres present in both Prokaryotes and Eukaryotes? Explain why some cells have telomeres and others don't. 4. A) Draw a cell with 2 pairs chromosomes as it goes through the cell cycle and indicate the main things that happen to its chromosomes at each stage (label: sister chromatids, homologous chromosomes,...
Please answer #19-21, explain and clearly indicate which # you are answering! Thank you in advance! 19. The c-abl gene is normally located on chromosome 9, and the bcr gene on chromosome 22. The abnormal fusion of these two genes resulting from a _______________ event is one of the leading causes of chronic myelogenous leukemia. A. paracentric inversion B. pericentric inversion C. non-reciprocal translocation D. reciprocal translocation E. duplication 20. A genetic counselor at a fertility clinic is assessing the...
1.a) How do we know that in humans the X chromosomes play no role in sex determination, while the Y chromosome causes maleness and its absence causes femaleness? c) How do we know that X chromosomal inactivation of either the paternal or maternal homolog is a random event during early development in mammalian females? d) How do we know that Drosophila utilizes a different sex-determination mechanism than mammals, even though it has the same sex-chromosome compositions in males and females?...
Coco Sex-Linked Problems (Alloles Located on the X Chromosome) of these problems, you do that humanae have one chrome and Ych males have two X chrom e They comecome does not carry the gene found on the X chromom genes that determine 11. Inhumans, the condition f cing (H) dominates the condition for onclotting the Both alleles are linked to the chrome made hemophilia maries a woman who is a carries for this condition in this specta carrier is a...
The following was gathered on
color blindness in one family. Color blindness in humans is an
X-linked recessive trait.
Indicate the genotypes for individuals 1 and 2 in generation
I.
Would it ever be possible for individuals 2 and 4 in generation
II to have a child with normal vision? Explain why or why not.
If individual 8 had a child, what would be the probability of
the child having normal vision?
Graded Assignment-2 Compatibility Mode] - Word (Product...
Given that TP53 is a recessive gene and is not located on the X chromosome, why would people who inherit just one mutant copy of a recessive tumor-suppressor gene be at higher risk of developing cancer than those without the recessive gene? Given that is a recessive gene and is not located on the X chromosome, why would people who inherit just one mutant copy of a recessive tumor-suppressor gene be at higher risk of developing cancer than those without...
Describe how the magnetic fields in z, x, and y; and the pulses and other timing are used to localize and influence the nuclear spins in a small vowel of tissue with an entire body placed in a MRI machine. Diagram the fields and timings and explain why. Explain the physics (Bloch Equations, etc.) of how an MRI image is made. Explain T1 and T2 weighting and what they measure best.