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Nucleotide excision repair is often employed when UV exposure causes the formation of what? a. phosphodiester bonds b. purine conjugates c. pyrimidine dimers d. tetrad disassembly

Short Answer

Expert verified
c. pyrimidine dimers

Step by step solution

01

- Identify the Question

Determine what the question is asking for. It is asking specifically what type of damage nucleotide excision repair is used to fix when caused by UV exposure.
02

- Understand the Options

Examine each of the provided options: a. phosphodiester bonds b. purine conjugates c. pyrimidine dimers d. tetrad disassembly
03

- Recall Knowledge about Nucleotide Excision Repair

Nucleotide excision repair is a mechanism used by cells to repair damage caused by UV light. This damage primarily leads to the formation of pyrimidine dimers, which include thymine or cytosine bases bonding together.
04

- Match the Correct Option

From the options, identify the one that correlates with the damage repaired by nucleotide excision repair. The correct answer is 'pyrimidine dimers' as UV light causes thymine or cytosine bases to dimerize.
05

- Confirm the Answer

Confirm that 'pyrimidine dimers' is the correct option for the damage repaired by nucleotide excision repair when caused by UV exposure.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Pyrimidine Dimers
Cells in our body work tirelessly to maintain the integrity of our genetic information. One major threat to this integrity is the formation of pyrimidine dimers. Pyrimidine dimers are formed when two adjacent pyrimidine bases in the DNA strand, usually thymine or cytosine, bond together. This abnormal bonding disrupts the normal pairing of DNA bases, leading to mutations during cell replication. This kind of damage makes it difficult for DNA polymerase to read the sequence correctly, which can result in incorrect bases being inserted and causes errors in the genetic code.
The consequence of pyrimidine dimer formation is significant, potentially leading to cancerous mutations. Hence, cellular mechanisms like nucleotide excision repair are crucial to detect and correct these mistakes, maintaining the fidelity of the DNA.
UV Damage
Ultraviolet (UV) light from the sun is a high-energy radiation that can damage the DNA in our cells. When skin is exposed to UV light, the DNA absorbs the energy from the UV rays. This can cause covalent bonds to form between adjacent thymine or cytosine bases, leading to the creation of pyrimidine dimers.
There are different types of UV light: UVA, UVB, and UVC, but UVB is most responsible for DNA damage in living organisms. UV damage can lead to mutations if not correctly repaired, and widespread DNA damage can initiate cancer.
Understanding UV damage has implications for public health. It underscores the importance of sunscreen and protective clothing to shield skin from excessive UV exposure, preventing the formation of these dangerous pyrimidine dimers.
DNA Repair Mechanisms
Our cells have evolved highly efficient DNA repair mechanisms to correct errors that occur due to UV exposure and other factors. One of the primary repair mechanisms for fixing pyrimidine dimers is nucleotide excision repair (NER).
In NER, the cell detects the distorted structure of the DNA helix caused by the dimer. Enzymes then cut out a short single-stranded segment of DNA containing the dimer. DNA polymerase fills in the gap with the correct nucleotides using the undamaged strand as a template. Finally, DNA ligase seals the newly synthesized patch into the existing strand, thus restoring the integrity of the DNA.
Without such effective DNA repair mechanisms, organisms would accumulate mutations leading to diseases like cancer. This highlights not only the remarkable resilience of biological systems but also the importance of understanding and protecting these processes.

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Most popular questions from this chapter

What are Okazaki fragments and how they are formed? a. Okazaki fragments are short stretches of DNA on the lagging strand, which is synthesized in the direction away from the replication fork. b. Okazaki fragments are long stretches of DNA on the lagging strand, which is synthesized in the direction of the replication fork. c. Okazaki fragments are long stretches of DNA on the leading strand, which is synthesized in the direction away from the replication fork. d. Okazaki fragments are short stretches of DNA on the leading strand, which is synthesized in the direction of the replication fork.

Prior to the work of Hershey and Chase, scientists thought that inheritance involved 鈥渘ucleoproteins.鈥 The amount of information to be transmitted between generations did not seem consistent with the chemical simplicity of the few nucleotides found in polymers of deoxyribonucleic acids in comparison to the diversity of protein polymers. Briefly explain: 鈥 the relationship between the structure of polymeric DNA and the information stored 鈥 the relationship between the interactions between base pairs on complementary strands of the double helix and Chargaff鈥檚 observation on the relative abundance of nucleotides in DNA 鈥 the meaning of the statement from the Nature publication on the structure of DNA by Watson and Crick: 鈥淚t has not escaped our notice that the specific pairing we have postulated immediately suggests a possible copying mechanism for the genetic material.鈥

Who was the first person to isolate the material that came to be known as nucleic acids? a. Frederick Griffith b. Friedrich Miescher c. James Watson d. Oswald Avery

A mutation has occurred in the DNA and in the mRNA for a gene. Discuss which would have a more significant effect on gene expression. Why? a. Both will result in the production of defective proteins. The DNA mutation, if not corrected, is permanent, while the mRNA mutation will only affect proteins made from that mRNA strand. Production of defective protein ceases when the mRNA strand deteriorates. b. Both will result in the production of defective proteins. The DNA mutation, if not corrected, is permanent, while the mRNA mutation will not affect proteins made from that mRNA strand. Production of defective protein continues when the mRNA strand deteriorates. c. Only DNA will result in the production of defective proteins. The DNA mutation, if not corrected, is permanent. Production of defective protein ceases when the DNA strand deteriorates. d. Only mRNA will result in the production of defective proteins. The mRNA mutation will only affect proteins made from that mRNA strand. Production of defective protein ceases when the mRNA strand deteriorates.

What are Autonomously Replicating Sequences (A R S)? a. areas of prokaryotic chromosomes that initiate copying b. portions of prokaryotic chromosomes that can be transferred from one organism to another c. areas of eukaryotic chromosomes that are equivalent to the origin of replication in E. coli d. portions of eukaryotic chromosomes that replicate independent of the parent chromosome

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