Question 1:
The answer is Deletion.
The most common reasons are
1. Point mutations in the controlling sequences or coding
region
2. Deletions in the controlling sequences or coding region
3. Gene amplification due to too much replication of one part of
the genome-this leads to multiple copies of the gene, which in turn
leads to too much protein
4. Induction by retroviruses (insertional mutagenesis)- a proviral
promoter may replace the cellular promoter and cause over
-expression.
Quesiton 2:
The answer is RB. It is a first identified Tumor-Suppressor
Gene.
The rest all are proto oncogenes.
According to HOMEWORKLIB RULES we have to answer one qeustion at a time. I answered two quesitons. Post the rest as seperate questions.
Which of the following is a common mutation resulting in the conversion of a proto oncogene...
Which type of mutation would not typically convert a proto-oncogene, such as beta- catenin, into an oncogene? O gene amplification O chromosomal deletion of the region containing the gene O mutation in the coding sequence that leads to the production of a hyperstable or hyperactive protein O chromosomal rearrangement that leads to overproduction of the normal protein DO 10 11 12 9 10 12 se $1 14 15 16 17 18 -13 14 15 16 17 18 13 19 20...
3) Proto-oncogenes can be converted to oncogenes by various genetic changes. Which of these mechanisms is not likely to contribute to conversion to an oncogene? Select one: A: Extra copies of the gene are made, thereby enhancing expression. B: A mutation occurs upstream of the gene that results in a more active promoter. C: Chromosomes break and fragments are translocated from one chromosome to another. D: Point mutations occur that result in a protein more resistant to degradation. E: All...
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...