ch 14 biology – Flashcards

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A chromosomal mutation where a segment breaks off, flips, and then reattaches itself is called a(n):
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duplication
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What is the difference between mismatch repair and nucleotide excision repair?
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In mismatch repair, one nucleotide is replaced, whereas in nucleotide excision repair several nucleotides are replaced.
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Sites in the genome that are more susceptible to mutations are called:
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hotspots
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True or false: DNA ligase is responsible for repairing thymine dimers caused by UV light.
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false
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True or false: A chromosomal mutation where a segment lacking a centromere breaks off is called a deletion.
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true
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True or false: Insertion of one nucleotide in a gene will lead to a frameshift mutation.
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true
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Which of the following mechanisms would most likely be involved in repairing a single point mutation?
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mismatch repair and or base excision repair
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When comparing DNA sequences of similar genes for proteins in related species, you see that some of the sequences are longer in one species compared to the other. Which of the following would most likely represent the extra number of bases that you would see?
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21
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Which of the following would describe the action of a chemical compound considered to be a mutagen?
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Most are reactive and add bulky side groups to DNA bases.
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The rates of evolutionary change in DNA:
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are highly variable among different gene families.
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A point mutation that causes a premature stop codon is called a:
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nonsense mutation
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DNA repair
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an involve excision of bases flanking a distortion in the helix
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Sickle-cell anemia is an example of what type of mutation?
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missense
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Which of the following mutations would most likely have the most severe consequence?
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frameshift
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Which of the following enzymes is responsible for initiating the proofreading repair mechanism?
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DNA polymerase
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True and false: Even though the chance of a mutation for one given nucleotide is rare, mutations are rather common when looking at the whole genome.
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true
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True or false: The use of antibiotics is creating the mutations in bacteria that make them resistant to these antibiotics.
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false
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True or false: Any deviation in normal gene dosage is lethal.
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false
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A person has a mutation in the gene for DNA uracil glycosylase. What is the most likely result of this mutation?
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an increase in mutations
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True or false: Movable DNA sequences that can "jump" from one spot in the genome to another are called transposable elements.
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true
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You are working in a lab studying a gene and notice that there are many other genes that code for similar traits.
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duplication and divergence
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Chronic myelogenous leukemia (CML) is caused when a segment of chromosome 9 and a segment of chromosome 22 both break off and switch places. How is this mutation classified?
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reciprocal translocation
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Which of the following would best describe the results seen in a flower whose sectors have different pigmentation?
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the result of transposable elements
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If DNA repair mechanisms were perfect, which of the following would most likely result?
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Evolution as we know it would stop because mutations are the only agent that gives us new genetic variation.
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What is one reason that RNA viruses and retroviruses have such a high rate of mutation?
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because RNA is more fragile than DNA and because viral polymerases lack a proofreading mechanism.
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Sites in the genome that are more susceptible to mutations are called:
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hotspots
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A chromosomal segment that breaks off and inserts into its homologous chromosome is what type of mutation?
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translocation
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True or false: Mutagens increase the amount of damage to DNA.
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true
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Mutations:
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can leave the protein sequence intact
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True or False: A point mutation is when a single nucleotide gets replaced by a different one.
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True
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A chromosomal mutation where a segment breaks off, flips, and then reattaches itself is called a(n) inversion. duplication. translocation. reciprocal translocation. deletion.
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Inversion
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True or False People with Xeroderma pigmentosum (XP) cannot properly execute base excision repair.
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False
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True or False The use of antibiotics is creating the mutations in bacteria that make them resistant to these antibiotics.
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False
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True or False Dosage refers to the number of copies of each gene in a chromosome.
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True
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The fact that humans have a relatively large number of mutations per genome per generation when compared to other organisms can be explained by: most of these mutations happen after reproduction, so they wouldn't be selected against. humans are so complex we have multiple proteins doing the same job. most of a human's DNA is noncoding, so most of the mutations are neutral. humans have multiple proteins doing the same job, and our cells don't divide as often as other those of other organisms. human cells don't divide as often as those of other organisms.
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most of a human's DNA is noncoding, so most of the mutations are neutral.
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True or False Any DNA "damage" is considered to be a mutation, even if it is immediately correct by the action of DNA polymerase.
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False
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True or False Loss of a pyrimidine base is one of the most common types of DNA damage.
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False
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Mutation rates (of nucleotides): are higher in organisms with larger genomes. are similar across all organisms. are lower in organisms with larger genomes. are highest in viruses. are highest in the bacteria.
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are highest in viruses.
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When comparing DNA sequences of similar genes for proteins in related species, you see that some of the sequences are longer in one species compared to the other. Which of the following would most likely represent the extra number of bases that you would see?
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21
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A gene that normally has the sequence CAGAGCCTATTAGGC is replicated as CAGAGCTGACGAGGC. Which of the following repair mechanisms would most likely be employed to fix this replication error? base excision repair nucleotide excision repair base excision repair and/or nucleotide excision repair DNA polymerase proofreading None of the answer options is correct.
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nucleotide excision repair
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Genetic risk factors? can increase the likelihood of somatic mutations. can increase the likelihood of germ-line mutations. can work synergistically with environmental risk factors. can be heritable. All of the answer options are correct.
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All of the answer options are correct.
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Which of the following would best describe the results seen in a flower whose sectors have different pigmentation? the result of the plant being triploid the result of the plant being tetraploid the result of a germ-line mutation the result of transposable elements the result of a deletion
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the result of transposable elements
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Which of the following statements concerning cancer and mutations is correct? Cancer can only occur with a mutation in a somatic cell. Cancer can only occur with a mutation in a germ cell. Usually multiple mutations are required in different genes to cause cancer. Usually a single mutation is all that is required to cause cancer. None of the answer options is correct.
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Usually multiple mutations are required in different genes to cause cancer.
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Which of the following statements is true concerning the work of the Esther and Joshua Lederberg? Their work demonstrated that mutations are determined by an organism's "needs." Their work demonstrated that mutations cannot occur randomly within organisms. Their work relied on a technique of bacterial culture known as "replica-plating," and demonstrated that mutations occur randomly within organisms. Their work relied on a technique of bacterial culture known as "replica-plating." Their work demonstrated that mutations in organisms arise in response to environmental conditions.
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Their work relied on a technique of bacterial culture known as "replica-plating," and demonstrated that mutations occur randomly within organisms.
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The amount of new mutations in living organisms following a round of genome replication: generally increases with larger genomes. generally decreases with larger genomes. is similar independent of genome size. is highest in the bacteria. None of the answer options is correct.
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generally increases with larger genomes.
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True or False Spontaneous mutations that occur in somatic cells will be transmitted to offspring.
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False
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What is one reason that RNA viruses and retroviruses have such a high rate of mutation? because RNA viruses and retroviruses initially cause mutations during replication because RNA replication is much more prone to mistakes because they lack a proofreading mechanism because RNA is more fragile than DNA and therefore more likely to be damaged because RNA is more fragile than DNA and because viral polymerases lack a proofreading mechanism.
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because RNA is more fragile than DNA and because viral polymerases lack a proofreading mechanism.
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Normally in corn, genes for waxy and virescent kernel appearance are linked. In a certain stock, however, it was found that these two genes assort independently. Which chromosomal aberration would explain this? translocation inversion duplication deletion None of the answer options is correct.
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Translocation
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Sickle-cell anemia is an example of what type of mutation? missense frameshift silent nonsense base pair deletion
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Missense
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The amount of new mutations in living organisms following a round of genome replication: generally increases with larger genomes. generally decreases with larger genomes. is similar independent of genome size. is highest in the bacteria. None of the answer options is correct.
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Generally increases with larger genomes
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_____ is the process where new genes evolve from duplicates of old ones. Reciprocal translocation Inversion Duplication and divergence Deletion Centromere dosage
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Duplication and divergence
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Which of the following would you expect to have the lowest nucleotide mutation rate? DNA viruses bacteria fruit flies humans RNA viruses
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Humans
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A trinucleotide of 5'CTC3' or 5'TTC3' is transcribed and then translated into the amino acid glutamic acid. A trinucleotide of 5'CAA3' or 5'TAC3' is transcribed and then translated into valine. In sickle-cell hemoglobin, valine is present instead of glutamic acid. Assuming a single base pair substitution has occurred, what is the mRNA code for valine in the affected mutant? GAA CUU GAG GUA
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GUA
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____ are locations in the genome where the sequence is incorrectly synthesized.
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Mutations
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_____ are cells of the body. We want low mutation rates in the cells of the body to preserve cellular integrity.
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Somatic cells
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_____ are produced by germ cells. Mutations in the germ cells can produce a heritable trait in the offspring.
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Gametes
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True or False: Mutation is quit common.
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True
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True or False: Lots of mutations don't actually cause disease, they just increase your risk.
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True
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ONE of the genes that controls the cell cycle does not by itself cause cancer, but it does substantially increase your risk of developing cancer. Instead of three subsequent mutation to the same cell line, it will only take _______ to result in cancer.
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2
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_____ change a single nucleotide
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Point mutations
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_____ occur either in non-coding DNA, or do not impact the amino acid coded for by the codon.
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Silent mutations
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Silent mutations are also known as a _______ mutation.
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synonymous mutation.
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_____ mutations are when an incorrect amino acid is incorporated into the protein. An example is sickle cell anemia.
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Missense
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Missense mutations are also known as a ____mutation.
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non-synonomous
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_______ mutation results when a stop codon is accidentally created. This causes protein synthesis to terminate pre-maturely.
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A nonsense
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A single point mutation results in incorrect _____ that results in red blood cells unable to carry oxygen.
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protein folding
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_____ elements are genes or gene fragments that can move throughout the genome. _____ can interfere with gene expression.
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Transposable , Transposons
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_____ mutations can result in the loss or gain of the genetic material.
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Chromosomal
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______ can result in offspring with two copies of a gene, or no copies of a gene. This is often how gene families develop. The mutated form of the gene may evolve a different function or may be turned on at different times.
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Duplication and deletion
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With ______ - there is a back up copy!
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gene function
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______is when a section of a chromosome is inserted in the reverse direction.
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Inversion
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A _____ translocation is when segments of non-homologous chromosomes switch places.
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reciprocal
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_____ can correct for incorrect base pairing, but requires deletion of several base pairs to excise the incorrect nucleotide.
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Mismatch repair
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______ excision repair excises and replaces a single incorrect or damaged nucleotide.
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Base
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_____ exision repair removes an entire segment of damaged DNA.
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Nucleotide
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______ are altered forms of base pairs.
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Tautomeres
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(TAUTOMERES) These damaged base pairs need to be removed through either _____ repair or ______repair.
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Base excision or nucleotide excision
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