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Biology 200, Summer 2012 Exam 2 VERSION A • Name: _________________________________ Section: _______ TA: _________________ Biology 200 Summer Quarter 2012 Exam #2 DO NOT OPEN EXAM UNTIL DIRECTED TO DO SO Make sure you have 6 pages, including this one. Print your name and information on ALL pages. • Please use a pen. Pen is much easier to read, even with extensive crossing-out. Pencil-written exams are acceptable, but it is often difficult to give full credit to penciled answers on regrades. • When asked, provide concise and clearly written answers. We may deduct points if you do not fully answer the question or if your answer is too vague or too confusing for us to follow. Extra information, if incorrect, will lose points. • Limit your answers to the space provided. If you need extra space, you can use the bottom of this first page. Indicate “on first page” where necessary. STOP STOP Page 1 of 6 STOP N Biology 200, Summer 2012 Exam 2 Name: _________________________________ Section: _______ TA: _________________ 1. (18 points) Fill in the blank For each, write TWO different answers that fit the description given. Be as specific as possible. It is acceptable to use the same answer for different questions. The full 3 points will be awarded for a correct pair of answers (+1 for a single correct answer). Ex) A type of gene implicated in cancer i. tumor suppressor ii. oncogene progression or mutation a) A metabolic energy carrier that is utilized before i. __________________ ii. __________________ the linking step and after glucose phosphorylation. b) An alternative to aerobic respiration that occurs in the absence of oxygen. i. __________________ ii. __________________ c) A transcription factor. i. __________________ ii. __________________ d) A molecule with lower redox potential than the electron-carrier Q (ubiquinone). i. __________________ ii. __________________ e) Growth media conditions that result in very i. __________________ ii. __________________ little ß-galactosidase production. 2. [15 points] Organelles For each organelle, describe the function of an enzyme that you would expect to find at that organelle and not in most other parts of the cell. The name of the enzyme is not necessary. You should mention a possible substrate and a reaction that is catalyzed. Answer each in one sentence or less. Be as specific as possible. Also, fill in the blanks with the number of the correct microenvironment that is created by the organelle. Each can be used only one time. +2 for each answer enzyme, +1 for each microenvironment. __7_Example) Chloroplast: Enzymes change small carbohydrates into Microenvironments larger carbohydrates using the energy from sunlight. 2) dilute & aqueous 3) acidic 6) basic 7) allows sunlight in 9) rich in lipid building blocks 11) low in mutating agents 14) rich in traffic-directing signal proteins 16) rich in motor proteins 17) non-cytoplasmic protein folding conditions ____a) Rough ER: ____b) Golgi apparatus: ____c) Lysosome: ____d) Nucleus: ____e) Cytoskeleton: Page 2 of 6 N Biology 200, Summer 2012 Exam 2 Name: _________________________________ Section: _______ TA: _________________ 3. [21 points] Gene Regulation a) (6 pts) You are developing an understanding of the similarities and differences between prokaryotes and eukaryotes. In 3-4 bullet points, describe 3 of the advantages that a single-celled prokaryote has over similar eukaryotes. Be as specific, clear, concise and thorough as possible. Complete sentences are not necessary. 1. 2. 3. 100 b) (3 pts) The Silver gene promoter: (Check ALL true answers): ____ Binds basal transcription factors tightly ____ Binds basal trancription factors poorly ____ Binds to regulatory transcription factors all of the time ____ Is NOT a double-stranded region of DNA AMOUNT of mRNA The data graph shows the total cellular levels of mRNA from 4 Black eukaryotic genes. Below the graph is a schematic of the transcription 80 and translation of the “Purple” gene. Each circle in the Purple protein represents an amino acid. Purple 60 Gold 40 Silver 20 5 min 10 min 15 min Time 20 min c) (3 pts) The Black gene is undergoing histone modification at Time 0. What type of change do you predict is taking place and why? Enter the correct word choice into the following. This causes [More or Less] acetylation of the histones? __________ This change in negative charges on the histone causes DNA to be [More or Less] tightly packed? ______ d) (3 pts) Imagine that over time, the Gold protein becomes more often targeted for modification by a ubiquitin ligase. How would the level of the gold protein change over time and why? Check in front of ALL correct answers. ___ ___ ___ ___ Gold Gold Gold Gold protein levels stay steady because the mRNA level is steady protein levels increase because Ubiquitin stabilizes proteins protein levels decrease because ubiquitin marks proteins for degradation protein levels are unpredictable because of the CAP protein e) (3 pts) The Purple protein can have either 10 or 13 amino acids. There is no change to the Purple gene DNA. Explain, including the location of the mechanism in the cell, in one sentence or less. DNA of Purple gene Immature mRNA of Purple gene Purple protein forms f) (3 pts) Which statements could explain the Purple data over time? (Check in front of ALL correct answers.) ____ At time 1 and 18, the conditions favor the activation of an enhancer protein for this gene ____ At time 12, the conditions favor the degradation of an enhancer protein for this gene ____ At time 1 and 18, the conditions favor the binding of a repressor ____ At time 12, the conditions favor the degradation of a silencer protein for this gene Page 3 of 6 N Biology 200, Summer 2012 Exam 2 Name: _________________________________ Section: _______ TA: _________________ 4. (16 points) The Kev Operon 5' 3' LBS2 LBS3 P Or1 Or2 ATG KevX TAG ATG KevW TGA ATG AUG UAG AUG KevP TAA UGA AUG 3' 5' UAA In the prokaryotic dsDNA shown above, Or1 and Or2 are operator sequences that can be bound by the repressor proteins R1 and R2, respectively. R1 and R2 are similar to the E. coli LacI protein. The coding regions for genes KevX, KevW and KevP are shown as well as the DNA sequences that encode the start and stop codons for each gene. LBS2 and LBS3 are DNA sequences that can be bound by the proteins T2 and T3, respectively. P is the promoter for the Kev operon. The proteins KevX and KevW are used to synthesize temporary protective proteins in the event of an attack by amoeba predators. a) (4 pts) This organism can recognize when there are no amoebae present. The prokaryote will react efficiently. When amoeba are gone: (Check in front of ALL correct answers.) ____ KEV X will be bound to LBS 2 ____ T2 will be bound to LBS 2 ____ R1 will be bound to OR 1 ____ KEV Y will be bound to OR2 ____ R2 will be bound to LBS 3 ____ T2 will be bound to OR 2 b) (4 pts) A mutation is analyzed that alters the UGA codon to a CGA codon. What would be the consequence of that mutation to the protein and to the cell? (Check in front of ALL likely consequences.) ____ The Kev mRNAs are produced normally ____ The Kev proteins are produced normally ____ The cell can fight amoeba normally ____ The Kev mRNAs have major errors ____ The Kev proteins have major errors ____ The cell is more vulnerable to amoeba c) (4 pts) T3 is a protein that activates transcription of the Kev operon. T2 lowers expression of Kev mRNA. Both proteins have DNA binding sites that are fairly similar (LBS2 and LBS3 have similar sequences). Besides the DNA binding region, what is true about the T2 and T3 proteins? (Check in front of ALL correct answers.) ___ ___ ___ ___ A surface of A surface of A surface of A surface of T2 T3 T2 T3 protein prohibits RNA polymerase binding protein prohibits RNA polymerase binding protein recruits RNA polymerase binding protein recruits RNA polymerase binding ___ ___ ___ ___ T2 allosterically inhibits T3 T3 allosterically inhibits T2 T2 is acting like the lac operon CAP protein T3 is acting like the lac operon CAP protein d) (4 pts) The KevP gene encodes a protein that can be released from the prokaryotes and digested by amoeba. If not digested, this protein will diffuse back into the prokaryote and bind tightly between P and Or1. Why is this logical for the regulation of Kev gene expression? (Answer in one sentence or less). Page 4 of 6 N Biology 200, Summer 2012 Exam 2 Name: _________________________________ Section: _______ TA: _________________ 5. [21 points] Cellular Respiration Shown below are several sets of 3 components from aerobic respiration. Put each set in correct order by labeling the first of the set with a “1”, second = “2”, 3 = last. You must have the entire order correct for credit, but there may be multiple correct orders for a single set. (3 points each) Example)_1_Glucose __3_ Krebs Cycle _2_Pyruvate a)___ ATP synthase ___ Linking step ___ Q electron transporter b) ___ Acetyl-CoA ___ proton motive force ___ commitment step c) ___ production of water ___ FADH2 ___ pyruvate d) ___ cytoplasmic NADH ___ production of CO2 ___ Complex IV e) ___ cutting a carbohydrate into two pieces ___ a series of oxidation reactions ___ transport into the mitochondria e) (3 pts) Eukaryotic mitochondria require a huge amount of ADP in order to create ATP. Where does all of that cellular ADP come from? Answer in 2 sentences or less. f) (3 pts) Choose one of the two statements below. Disagree with the statement, and support your argument. Make your case in 2 sentences or less. You only need to complete one argument. Statement #1: The purpose of the Kreb’s cycle is to oxidize carbon-containing molecules. Statement #2: A eukaryotic organism would rather consume pyruvate than glucose. I disagree with statement # ____ because: Page 5 of 6 N Biology 200, Summer 2012 Exam 2 Name: _________________________________ Section: _______ TA: _________________ Take Home: Cancer History Cancer is a complex and extremely diverse system of related diseases. We know that these diseases are the result of multiple mutations in cells causing an array of intracellular changes. No single mutation is cancer. Somehow, the combinations of multiple changes lead to malignant unregulated cell growth. 6. (8 points) Your task is to define a few possible mutations that could contribute to cancer. For each mutation, you should indicate as specifically as possible how the mutation occurred, where in the cell and in the body the mutated cell is located, and the mechanism that allows this mutation to lead to cancer. Be creative where necessary. You should do this in less than one sentence for each mutation (If necessary, you can use two short sentences). Research outside of Bio200 lectures and labs is not necessary, but is allowed if you want to find specific examples of parts of this question. Show the diversity of what you know: mutation descriptions should be as different from each other as is possible while still being specific and correct. Example) This mutation is in a gene that encodes a signaling molecule to start apoptosis. A random DNA polymerase III error in a white blood cell’s signal receptor gene causes the loss of social control so that the cell won’t kill itself when it picks up further DNA damage. a) This mutation is in a gene that either encodes a cytoskeletal molecule or an enzyme that works on a cytoskeletal molecule. b) This mutation is in a gene whose product works in or travels through the Golgi apparatus. c) This mutation affects the passage of the cell through the cell cycle. 9. (4 points) Given the mutations you’ve described, imagine a cell with all three mutations. Write a description of an additional mutation that would be needed for this cell to progress further towards outright malignant cancer. Again, a single sentence should be enough room to be specific, creative, and correct. Page 6 of 6 N