Question 1 Origin 5' 3' 3 5' Unwinding Unwinding Origin Question 1: The following diagram (below) represents the template strands of a replication bubble in a DNA molecule. Draw in the newly synthesized strands and label the leading and lagging strands.
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![Question 1
Origin
5'
3'
3
5'
Unwinding
Unwinding
Origin
Question 1: The following diagram (below) represents the template strands
of a replication bubble in a DNA molecule. Draw in the newly synthesized strands
and label the leading and lagging strands.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F848c2a05-1a16-41e5-afb3-dbc0d9ef5cb6%2Fe6aa5a58-9e47-423c-8287-861aab0f6a17%2Fhlzdosoe_processed.jpeg&w=3840&q=75)
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- Question 6 Match term and its description. heat briefly separate DNA strands [ Choose ] cool to allow primers to form hydrogen bonds with ends of | Choose sequence. DNA polymerase adds nucleotides to the 3' of each primer [ Choose )QUESTION 1 The sequence of a DNA including the gene that you want to clone into a plasmid vector. The gene of interest is in bold with the stop codon shown in green. The sequence has no suitable restriction site for digestion to isolate the gene fragment for cloning. Recognition site of Sal-I enzyme is given below. Design a primer to introduce the Sal-I site to the beginning of the gene. Write the complementary DNA sequence Design the primer and show which strand of DNA it is complementary to Mark the direction of all DNA sequences including the primer. 5-TGTCAGCACCATCTGTCCGGTCCCAGCATGCCTTCTGAGACCCAGGCAG(1500b)TGGGGCTGACTCTTTA-3 Sal-1 recognition site GTCGAC CAGCTG THIS IS COMPLETE QUESTION. PLEASE EXPLAIN EACH PART OF GTHE QUESTION.Question 3. How is the primer different in eukaryotic DNA replication than prokaryotic DNA replication?
- Question 8. You isolate the DNA from the bacterial cells and apply the Sanger dideoxy sequencing method. You then separate the products of the reactions by gel electrophoresis and obtain the following pattern. What is the sequence of the template and the DNA on the gel? ddATP ddTTP ddCTP ddGTP Template V [ Choose 3'-CTAGTCAAGG-5' 5'-CTAGTCAAGG-3' Sequence 3'-GATCAGTTCC-5' 5'-GATCAGTTCC-3' 5'-GGAACTGATC-3'QUESTION 20 Careful TEM studies suggested that histone octamers get removed during DNA replication. This raised a question regarding what happens to the histone octamers after they get removed. Do the histone octamers get disassembled after removal, or do they remain intact and get added back onto the DNA without disassembly. The figure below outlines an experiment that researchers performed to address this question. In a single sentence, describe the conclusion that can be drawn from this experiment. Experiment Question: What happens to histones in eukaryotic DNA replication? Methods 1 Grow cells for several generations in a medium that contains amino acids labeled with a heavy isotope. 2 Transfer the cells to a medium that contains amino acids labeled with a light isotope. Results Change medium Replication Isolate octamers 3 Isolate histone octamers before and after replication... Spin 4 ...and subject them to density-L gradient centrifugation. 5 Newly synthesized octamers are less…QUESTION 6 These correct “overwinding” ahead of the replication forks by breaking, swiveling, and rejoining DNA strands. Helicases Single-strand binding proteins Topoisomerase Telomerase
- QUESTION 9 These are enzymes that untwist the double helix at the replication forks of replicating DNA. Helicases Stingle-strand binding proteins Topoisomerase TelomeraseQUESTION 1 For the DNA structure below write the correct base sequence in the form: 5'-ATCT-3' 3'-TAGA-5' Make sure you include the 5' and 3' to indicate strand polarity as shown above. Hydrogen bondQuestion 2. For your senior research, you end up studying the life cycle of an animal virus whose genome consists of a single circular, double-stranded DNA molecule. Your project is to define the number and location of the origin(s) of replication and to determine whether replication proceeds in one (unidirectional) or both (bidirectional) directions away from an origin. To accomplish this, you isolate many identical strands of DNA that have already been partially replicated. You cleave each piece of DNA exactly once with a restriction enzyme. You then observe the cut pieces of DNA using an electron microscope. Below is a schematic representation of what you observe. Remember that each line represents a different piece of DNA, and not a fragment of a larger piece. Using this data, answer the following questions: A) How many origins of replication do you think the viral genome has, and why do you think this? 30: F2 #3 *** E D 80 F3 54 $ 4 F4 R LL % 5 F5 T G B) Do your data support…
- Question 6 1 pts You are assembling the genome sequence of a newly discovered bacterium by aligning a set of BAC clones. Correct assembly requires O spacer regions O repeated sequences O overlapping sequencesQuestion 4 About endonucleases: A Restriction endonucleases always cut double-stranded DNA and are endo- deoxyribonucleases. B Once the DNA sequence is recognized, they cleave the bond between the desoxyri- bose and the nitrogenous base. |C| they are proteins that are necessary for the replication of DNA. they act on single-stranded DNAS, RNAS, and double-stranded DNAS. E they are enzymes whose substrate is a double-stranded sequence of nucleic acids, DNA or RNA, or hybrid DNA-RNA.QUESTION 5 If you ran the amplicon from the previous question (so it's about 3.7k basepairs long), on a gel, what would you want your gel to look like after you stain it with ethidium bromide and look at it under UV, assuming you ran it next to a 1kb DNA ladder? O A. A lot of lighter bands below the 4kb band O B. A very bright band at the bottom of the gel, and a lighter band in the middle of the gel. O C.A bright smear O D. one bright band that lines up between the 3kb and 4kb ladder band. Should be above the 3kb band (closer to the wells). O E. one bright band that lines up below the 3kb ladder band (further from the wells)
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