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Combined_Final__v6_no_keyBiology 101 – Midterm 1 –Spring 2024

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Biology 101 – Midterm 1 –Spring 2024 Dr. Betley, Dr. Wagner Your signature below certifies that you have complied with the Code of Academic Integrity of the University of Pennsylvania in taking this exam. This code will be strictly enforced! Signature Your Name (print): Check the name of your lab instructor and circle your lab section: Arielle Levine 108 Staver Bezhani 101 102 103 104 105 • DO NOT OPEN YOUR EXAM UNTIL YOU ARE TOLD TO DO SO. • Please print your first and last name on EVERY page of the exam. • This is a closed book exam. You will have 110 minutes to complete the exam. • Make sure you have a complete exam (13 pages). • You must use a pen to complete this exam. Do not use red ink, pencil or white-out on the exam. • No calculators or smartphones may be used during the exam. Phones must be turned off or silenced and put away during the exam. If you are found using a smartphone or calculator during the exam, you will be reported to the Office of Student Conduct. • Please be sure to budget your time so that you can complete the entire exam. To answer the multiple choice questions, circle the letter of the single best answer and write the letter of that answer in the space provided. • If a question appears ambiguous, ask a proctor; proctors will answer questions only if they feel that your question reveals a genuine ambiguity in the wording of the question. Page Questions Possible Points Points Received 2 3 4-13 Score total for 100 point value of exam: ________ Score total for 90 class points:___________ Question 1. (7.5 points) Genetics. Crossover happens between genes far away on the same chromosome, and one crossover event yields recombinant chromosomes out of the 4 final chromosomes generated by meiosis. Two genes close to each other on the same chromosome that yield fewer than the expected number of recombinants are called genes. Such genes do not follow Mendel’s second law, the law of . A chromatid is a chromosome that has undergone DNA , resulting in two double stranded DNA helices. The error rate of copying the DNA in S phase is very low, hence the two chromatids have the DNA sequence. Question 2. (10 points) Mutations A. Which of these mutations is likely to destroy function of a protein? Circle all that are correct. B. Which of them might give rise to a dominant mutation? Write D next to all that apply. a. frameshift b. small deletion in the coding region c. deletion of the entire gene d. point mutation at a wobble base that does not change the primary amino-acid sequence e. mutation in the enhancer that leads to more binding of a transcriptional activator f. point mutation in the coding region that enhances activity of the protein g. small insertion in the coding region h. mutation in the active site that allows the protein to bind an additional substrate i. mutation in a splice donor site that leads to failure to splice out an intron Question 3 (6 points). All of the statements below have one error in them. Please correct the error by changing (adding, removing or replacing) one word. Splicing is carried about by an RNA/protein complex, the spliceosome. After the 5’ donor site of the intron is cleaved, it is transferred to the branch site. After a cut is made at the 3’ intron splice acceptor site, the 3’ end of the first exon is fused to the 5’ end of the second exon, completing exon removal. A charged tRNA, a ribosome with ribosomal RNA, and mRNA are required for translation. The aminoacyl synthase charges the tRNA with the amino acid that matches its anticodon. The release factor (a protein that matches the stop codon) terminates the polypeptide chain, and sigma factors plus a special Methionine tRNA start translation. After mRNA production, splicing, 3’ polyadenylation and 5’ capping occurs. The capping involves a ligation of a nucleotide, a G, at the 5’ position of its ribose to the 3’ end of the mRNA. Polyadenylation involves a new enzyme, polyA polymerase, which adds A’s to the end of the mRNA after the transcription termination signal. .................................................continued.............................................

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Name:


Biology 101 – Midterm 1 –Spring 2024 Dr. Betley, Dr. Wagner

Your signature below certifies that you have complied with the Code of Academic Integrity of the
University of Pennsylvania in taking this exam. This code will be strictly enforced!

Signature

Your Name (print):

Check the name of your lab instructor and circle your lab section:


Arielle Levine 108

Staver Bezhani 101 102 103 104 105

• DO NOT OPEN YOUR EXAM UNTIL YOU ARE TOLD TO DO SO.

• Please print your first and last name on EVERY page of the exam.

• This is a closed book exam. You will have 110 minutes to complete the exam.

• Make sure you have a complete exam (13 pages).

• You must use a pen to complete this exam. Do not use red ink, pencil or white-out on the exam.

• No calculators or smartphones may be used during the exam. Phones must be turned off or silenced
and put away during the exam. If you are found using a smartphone or calculator during the exam,
you will be reported to the Office of Student Conduct.

• Please be sure to budget your time so that you can complete the entire exam.

To answer the multiple choice questions, circle the letter of the single best answer and write the letter
of that answer in the space provided.

• If a question appears ambiguous, ask a proctor; proctors will answer questions only if they feel
that your question reveals a genuine ambiguity in the wording of the question.
Page Questions Possible Points Points Received
2 1-11 15
3 12-15 21
4-13 MC 1-32 64
Total 100




Score total for 100 point value of exam: ________ Score total for 90 class points:___________

1

, Name:



Question 1. (7.5 points) Genetics. Crossover happens between genes far away on the same

chromosome, and one crossover event yields recombinant chromosomes out

of the 4 final chromosomes generated by meiosis. Two genes close to each other on the same

chromosome that yield fewer than the expected number of recombinants are called

genes. Such genes do not follow Mendel’s second law, the law of

. A chromatid is a chromosome that has undergone DNA

, resulting in two double stranded DNA helices. The error rate of

copying the DNA in S phase is very low, hence the two chromatids have the

DNA sequence.



Question 2. (10 points) Mutations

A. Which of these mutations is likely to destroy function of a protein? Circle all that are correct.

B. Which of them might give rise to a dominant mutation? Write D next to all that apply.

a. frameshift
b. small deletion in the coding region
c. deletion of the entire gene
d. point mutation at a wobble base that does not change the primary amino-acid sequence
e. mutation in the enhancer that leads to more binding of a transcriptional activator
f. point mutation in the coding region that enhances activity of the protein
g. small insertion in the coding region
h. mutation in the active site that allows the protein to bind an additional substrate
i. mutation in a splice donor site that leads to failure to splice out an intron




Question 3 (6 points).



2

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