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- A research paper published in the summer of 2012presented a method to obtain the whole-genome sequence of a fetus without any invasive procedure suchas amniocentesis that could on rare occasions causemiscarriage. This new technique is based on the factthat some fetal cells leak into the mother’s bloodstream and then break down, releasing their DNA.Assume that exactly 10% of the DNA fragments inthe mother’s blood serum come from the fetus, whilethe remaining 90% of the DNA fragments in the serum come from the mother’s genome.The investigators collected cell-free DNA from apregnant woman’s bloodstream and subjected it to anadvanced high-throughput sequencing method. Thetable at the end of this problem looks at seven unlinked loci; the number of reads of particular alleles(identified by Greek letters) are shown. You shouldassume for the sake of simplicity that all numericaldifferences are statistically significant (even thoughactual data are never this clean).a. Determine whether each…When the DNA of a human cell becomes damaged, the p53 geneis activated. What is the general function of the p53 protein?Is it an enzyme, transcription factor, cell-cycle protein, orsomething else? Describe three ways in which the synthesisof the p53 protein affects cellular function. Why is it beneficialfor these three things to happen when a cell’s DNA hasbeen damaged?The best estimate is that the human genome containsfewer than 21,000 genes. However, there is evidencethat human cells produce many more than 21,000 different polypeptides. What processes might account for thisdiscrepancy?
- If you expose human tissue culture cells (for example,HeLa cells) to 3H-thymidine just as they enter Sphase, then wash this material off the cells and letthem go through a second S phase before looking atthe chromosomes, how would you expect the 3H to bedistributed over a pair of homologous chromosomes?(Ignore the effect recombination could have on thisoutcome.) Would the radioactivity be in (a) one chromatid of one homolog, (b) both chromatids of one homolog, (c) one chromatid each of both homologs,(d) both chromatids of both homologs, or (e) someother pattern? Choose the correct answer and explainyour reasoning. (This problem extends the analysisbegun in Solved Problem III.)Your friend sends you two cancerous cell lines to examine and determine possible mutations. The results are shown below: Cell Line Mutation WT none (wild type DNA) 1 a deletion at the same region on both copies of chromosome 4 a point mutation in a gene on only one copy of chromosome 7 Based on this data, what type of geńe is mutated in each of the cell lines? Select all that apply O Cell line 2 has a mutation in an oncogene Cell line 1 has a mutation in a tumor suppressor gene Cell line 1 has a mutation in an proto-oncogene Cell line 2 has a mutation in a tumor suppressor geneWhen 1 million cells of a culture of haploid yeastcarrying a met− auxotrophic mutation were plated onpetri plates lacking methionine (Met), five coloniesgrew. You would expect cells in which the originalmet− mutation was reversed (by a base change back tothe original sequence) would grow on the media lackingmethionine, but some of these apparent reversions couldbe due to a mutation in a different gene that somehowsuppresses the original met− mutations. How wouldyou be able to determine if the mutations in your fivecolonies were due either to a precise reversion of theoriginal met− mutation or to the generation of a suppressor mutation in a gene on another chromosome?
- Look at the two yeast colonies in Figure Q4–3. Eachof these colonies contains about 100,000 cells descendedfrom a single yeast cell, originally somewhere in the mid-dle of the clump. A white colony arises when the Ade2 geneis expressed from its normal chromosomal location. Whenthe Ade2 gene is moved to a location near a telomere, itis packed into heterochromatin and inactivated in mostcells, giving rise to colonies that are mostly red. In theselargely red colonies, white sectors fan out from the middleof the colony. In both the red and white sectors, the Ade2 gene is still located near telomeres. Explain why white sec-tors have formed near the rim of the red colony. Based onthe patterns observed, what can you conclude about thepropagation of the transcriptional state of the Ade2 genefrom mother to daughter cells in this experiment?Roman 16px : 1.0pt : BIUS A A X2 x E tion of chromosomes did not occur berore cytoknESIS, 1/2 the # of chromsomes or 1 of each b. If the situation in part a occurred, would the new cells be viable? Explain. no, it wouldnt have the DNA OP 10. The S phase stands for synthesis, which means to make or build something more complex out of simpler parts. Scientists know that during the S phase DNA is being made in the nucleus of the cell. Why do you think the cell needs to make more DNA at this time in the cell cycle? 11. Refer to Model 1. The chromosomes that are shaped like "X" (made of two sister chromatids) have double the amount of DNA than the chromosomes that are shaped like "I." During what phase of the cell cycle do you think the chromosomes are replicated (copied)? POGIL Activities for High School Biology 2. hpIn the Avery MacLeod experiment it was assumed that P32 only labels DNA and not protein. would this be ture in all cellular systems?Why or why not?
- Which of the following genetic mechanism isn't used by bacteria in the transference of genetic resistance to antibiotics? Which of the following genetic mechanisms is not used by bacteria in the transfer of antibiotic resistance? Select one: O transduction O conjugation O through transposons O transformation O crossing over between homologous chromosomes Which of the following is not consider one of the main factors in the emergence of antibiotic resistance? O a. an increase in immuocompromised patients f O b. increase O c. failures on the staff O d. an increase in antibiotic resistance pathogensThe family of a sixth-grade boy in Palo Alto, California, wasinformed by school administrators that he would have to transferout of his middle school because they believed his mutation ofthe CFTR gene, which does not produce any symptoms associatedwith cystic fibrosis, posed a risk to other students at the schoolwho have cystic fibrosis. After missing 11 days of school, a settlementwas reached to have the boy return to school. What ethicalproblems might you associate with this example?The cells from a person’s malignant tumor were subjected to insitu hybridization using a probe that recognizes a unique sequenceon chromosome 14. The probe was detected only once in each ofthe cells. Explain this result, and speculate on its significance withregard to the malignant characteristics of these cells.