Exam 2 Flashcards
In a DNA double helix:
A. purines pair with purines B. the 2 DNA strands run parallel C. the 2 DNA strands are identical D. the 2 DNA strands run antiparallel E. thymine pairs with cytosine
D. the 2 DNA strands run antiparallel
The Central Dogma specifies that the information in:
A. DNA is copied directly into a protein.
B. DNA is copied into an RNA molecule during transcription, and the information in that RNA molecule is used to make a protein during translation.
C. RNA is copied into a DNA molecule during transcription, and the information in that DNA molecule is used to make a protein during translation.
D. DNA is copied into an RNA molecule during translation, and the information in that RNA molecule is used to make a protein during transcription.
E. Protein is copied into an RNA molecule during translation, and the information in that RNA molecule is used to make DNA during transcription.
B. DNA is copied into an RNA molecule during transcription, and the information in that RNA molecule is used to make a protein during translation.
Which of the following chemical groups is NOT used to construct a DNA molecule?
A. nitrogen-containing base B. five-carbon sugar C. all of the above D. phosphate E. six-carbon sugar
E. six-carbon sugar
The DNA from 2 different species can often be distinguished by a difference in the
A. ratio of A + T to G + C B. none of the above C. ratio of A + G to C + T D. presence of bases other than A, G, C, and T E. ratio of sugar to phosphate
A. ratio of A + T to G + C
If 30% of the nitrogenous bases in a sample of DNA (double-stranded) from Drew, your PAL tutor, are cytosine, what percentage should be thymine?
20%
For a science fair project, Aleena and Barrett decided to repeat teh Hershey and Chase experiment, with modifications. They decided to radioactively label the nitrogen of the DNA, rather than the phosphate. They reasoned that each nucleotide has only one phosphate and 2:5 nitrogen atoms. Thus, labeling the nitrogen atoms would provide a stronger signal than labeling the phosphates. Why won’t this experiment work?
A. Amino acids (and thus proteins) also have nitrogen atoms; thus, the radioactivity would not distinguish between DNA and proteins.
B. Radioactive nitrogen has a half-life of 100,000 years, and the material would be too dangerous for too long.
C. Although there are more nitrogen’s in a nucleotide, labeled phosphates actually have 16 extra neutrons; therefore, they are a more radioactive.
D. The science fair is to blame.
E. There is no radioactive isotope of nitrogen.
A. Amino acids (and thus proteins) also have nitrogen atoms; thus, the radioactivity would not distinguish between DNA and proteins.
A world-renowned pathologist, Claire Ward, studies 2 strains of Streptococcus pneumonia, one that causes a lethal infection when injected into mice, and a second that is harmless. She observes that pathogenic bacteria that have been killed by heating can no longer cause an infection. But when these heat-killed bacteria are mixed with live, harmless bacteria, this mixture is capable of infecting and killing a mouse. what would Claire conclude from her experiment?
A. The infectious strain cannot be killed by heating.
B. The mice had lost their immunity to infection with S. pneumoniae.
C. The heat-killed pathogenic bacteria “transformed” the harmless strain into a lethal one.
D. I am Claire. I made this question and forgot.
E. The harmless strain somehow revived the heat-killed pathogenic bacteria.
C. The heat-killed pathogenic bacteria “transformed” the harmless strain into a lethal one.
The human genome is a diploid genome. However, when germ-line cells produce gametes, these specialized cells are haploid. What is the total number of chromosomes found in each of the gametes (egg or sperm) in your body?
A. 46 B. 23 C. 22 D. 23 + X or Y E. 44
B. 23
Which statement is true about the association of histone proteins & DNA?
A. Each histone protein has a deep groove into which a DNA double helix tightly fits.
B. Histone proteins have a high proportion of positively charged amino acids, which bind tightly to the negatively charged DNA backbone.
C. Histone proteins from hydrogen bonds with the nucleotide bases of DNA.
D. Histone proteins have a high proportion of negatively charged amino acids, which bind tightly to the positively charged DNA backbone.
E. Histone proteins insert themselves into the major groove of DNA.
B. Histone proteins have a high proportion of positively charged amino acids, which bind tightly to the negatively charged DNA backbone.
Which of the following statements is NOT true?
A. A cell will temporarily decondense its chromatin to give proteins rapid. localized access to specific DNA sequences.
B. When a cell divides, its chromatin structures will typically be inherited by its daughter cells.
C. A cell will temporarily decondense it chromatin to silence genes during differentiation.
D. A cell can permanently condense and silence an entire chromosome during development.
E. A cell will temporarily decondense its chromatin to allow access to specific DNA sequences for replication, repair or gene expression.
C. A cell will temporarily decondense its chromatin to silence genes during development
You prepare bacterial extracts by lysing the (circular bacterial) cells and removing insoluble debris via centrifugation. These extracts provide the proteins required for DNA replication. Your DNA template is a small, double-stranded circular piece of DNA (a plasmid) with a single origin of replication and a single replication termination site. The termination site is on the opposite side of the plasmid from the origin. What part of the DNA replication process would most directly be affected if a strain of bacteria lacking helicase were used to make the cell extracts?
A. Okazaki fragment synthesis B. termination of DNA synthesis C. leading-strand elongation D. lagging-strand completion E. initiation of DNA synthesis
E. initiation of DNA synthesis
! Which statement is FALSE?
A. DNA helicase produces transient nicks in the DNA backbone to relieve the tension built up by the unwinding of DNA ahead of the DNA to poison erase.
B. Single-strand DNA -binding protein binds to single-stranded DNA exposed by DNA helicase, preventing base pairs from re-forming before the lagging strand can be replicated.
C. DNA ligase uses the energy of AT hydrolysis to join Okazaki fragments made on the lagging-strand template.
D. Sliding clamp keeps DNA polymerase attached to the template, allowing the enzyme to move along without falling off as it synthesizes new DNA.
E. Primate synthesizes RNA primers along the lagging-strand template.
A. DNA helicase produces transient nicks in the DNA backbone to relieve the tension built up by the unwinding of DNA ahead of the DNA to poison erase
NOT — Sliding clamp keeps DNA polymerase attached to the template, allowing the enzyme to move along without falling off as it synthesizes new DNA — whic is TRUE
Which of the following statements is NOT an accurate statement about thymine dimers?
A. Thymine dimers are covalent links between thymidines on opposite DNA strands.
B. Thymine dimers cannot be repaired.
C. Thymine dimers can cause the DNAr explication machinery to stall.
D. Prolonged exposure to sunlight causes thymine dimers to form.
E. Repair proteins recognize thymine dimers as a distortion in the DNA backbone.
A. Thymine dimers are covalent links between thymidines on opposite DNA strands.
Which statement is TRUE?
A. homologous recombination cannot occur in prokaryotic cells, because they are haploid, and therefore ahve no extra copy of the chromosome to use as a template for repair.
B. The DNA template used to repair the broken strand is the homologous chromosome inherited from the other parent.
C. After damaged DNA has been repaired, nicks in the phosphate backbone are maintained as a way to identify the strand that was repaired.
D. Nonhomologous end joining is a mechanism that ensures that DNA double-strand breaks are repaired with a high degree of fidelity to the original DNA sequence.
E. all of the above
E. all of teh above
Beki Gjyzeli and Lilliana Burton win No-Bell prize in 2021 for their discovery for the molecular mechanisms of DNA repair. Their discovery shows that double-strand DNA breaks caused by ionizing radiation often miss nucleotides at the broken ends. According to their discovery, what type of repair would likely be used, and what would be the result of repairing this type of damage?
A. Nonhomologous end joining would e used and would lead to properly repaired DNA.
B. If duplicated intact chromosomes are not available, nonhomologous end joining would be used to joint the DNA, but errors would still remain.
C. Direct repair would be used and would lead to properly repaired DNA.
D. DNA Mismatch repair would be used and would lead to properly repaired DNA.
E. Direct repair would be used to join the DNA, but errors would still remain.
B. If duplicated intact chromosomes are not available, nonhomologous end joining would be used to join gate DNA, but errors would still remain.
The energy for DNA polymerization is provided by the hydrolysis of which of the following?
A. incoming nucleoside triphosphates (releasing PPi)
B. the 3’ end of the growing stand (releasing H2O)
C. GTP (releasing Pi)
D. ATP (releasing Pi)
E. pyrophsophate (releasing Pi)
A. incoming nucleoside triphosphates (releasing PPi)
Which statement is true?
A. DNA synthesis in the 3’-to-5’ direction is chemically possible
B. In living systems, DNA synthesis in the 3’-to-5’ direction does not allow proofreading.
C. If DNA synthesis would occur in the 3’-to-5’ direction in living systems, there is no favorable hydrolysis reaction to drive the addition of new nucleotides once a mispaired nucleotide is removed.
D. The synthesis of DNA in living systems occurs in the 5’-to-3’ direction.
E. all of the above
E. all of the above
Which of the following statements from our classmates is true?
A. Regan: DNA synthesis begins near promoter regions called replication origins. G and C nucleotides are rich in these regions.
B. Katie: ribosomal RNAs are synthesized and combined with proteins to form ribosomes in the Er & Golgi.
C. Addie: Primase requires a proofreading function that ensures that there are no errors in the RNA primers used for DNA replication.
D. Kaci: The attachment of single-strand DNA-binding proteins to the lagging-strand template powers thea cation of helicase the replication fork, where it opens up the double helix.
E. Autumn: Primase is needed to initiate DNA replication on both the leading strand and the lagging strand.
E. Autumn: Primase is needed to initiate DNA replication on both the leading strand and the lagging strand.