Explain why a gain-of-function mutation to a proto-oncogene (or its promoter) may be associated with increased risk of cancer. (b) Explain why a loss-of-function mutation to a tumor suppressor gene may be associated with increased risk of cancer.
a)proto-oncogene are the genes which promote in the cell division or prevents cell death so when such genes or it`s promoter is mutated such that it`s expression increase it will increase the risk of cancer because the cells will divide more and more or cell will not undergo apoptosis. these type of mutations which increases it`s expression make protooncogene an oncogene. Increased cell division and no cell death leads to cancer.
b) tumour suppressor genes are those genes which control cell growth or genes which induce apoptosis when these genes are mutated such that it losses it`s function there will be no control over cell growth so cells divide more and more leading to cancer so loss of function mutations in tumour suppressor gene may be associated with increased risk of cancer, there are many other factors controlling cell division so loss of function mutation in tumour suppressor genes increases the chance or cancer.
Explain why a gain-of-function mutation to a proto-oncogene (or its promoter) may be associated with increased...
Explain why a mutation in only one of two copies of a proto-oncogene in a diploid cell can promote the development of cancer (5 points), whereas both copies of a tumor-suppressor gene need to be mutated to do likewise (5 points).
Indicate whether each of the following descriptions applies to an oncogene, a proto-oncogene, or a tumor suppressor gene. Some descriptions may apply to more than one of these gene types. Drag the gene types on the left to the appropriate blanks on the right to match the descriptions. Gene types can be used once, more than once, or not at all. Reset Help oncogene - gene(s) whose presence can cause cancer. proto-oncogene -gene(s) whose absence can cause cancer. tumor suppressor...
2) What is the most likely phenotype of a loss of function mutation in a proto-oncogene? (you may select more than one answer) a) Increased cell division b) decreased cell division c) cancer d) non-disjunction
13. Which of these statements is TRUE? a. Cancer cells usually have more than one mutation. . Proto-oncogenes are normal genes that code for proteins that cause cells to undergo apoptosis (programmed cell death) c. Cancer usually involves a gain-of-function mutation in a tumor suppressor gene d. Cancer usually involves a loss-of-function mutation proto-oncogene
Label the following as either proto-oncogene, oncogene or tumor suppressor 3. A gene that initiates apoptosis when DNA damage occurs a. b. A gene that initiates the transition from G1 to S phase A gene that inhibits the transition from G1 to S phase c. d. A gene that promotes cell growth, combined with a hyperactive promoter How would methylation of the promoter of the gene in question 3c affect the cell? Be specific using what you know about the...
Cancer and Gene Regulation Why is a cell cycle control system needed for cell division? What happens when cells do NOT respond to the cell cycle control system and divide excessively? Tumor Proto-oncogeno (for protein that stimulates coll division) 6 Y DNA Benign Tumor= Mutation withln a control region of DNA Malignant Tumor Mutated promoter Metastasis Normal growth-stimulating protein in excess Oncogene Tumor-Suppressor Genes Proto-oncogene utled tara gese Samor-auppresr gane Many proto-oncogenes code for growth factors /Deletive nonimenig Normel grewt...
Help 45. A region of the chromosome 1000 base pairs upstream of the promoter for the gene pbxH was deleted. This resulted in decreased expression of pbxH. This region is most likely a/an A. intron B. gene for a transcription factor C. gene for the RNA polymerase D. proximal control region E. enhancer 46. Methylation (actually, increased or hypermethylation) of the GSTP1 promoter is a common DNA alteration in certain cancers. Which of the following best characterizes this alteration? A....
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...
IN CONTEXT OF GENE EXPRESSION AND PROTEIN SYNTHESIS OUTCOME 5. a), Why are Proto-Oncogenes important for the cell cycle control and what is their implication in a progression of tumors and cancers? Provide examples of TWO proto-oncogenes and a type of a cancer each is associated with. (6 pts) b) Now consider the diagram below. Under each of three scenarios, explain a likely cellular consequence relative to gene expression and protein synthesis outcome, assuming each could lead to a development...
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...