Replication Flashcards

1
Q

What are the components of a nucleotide?

A

A nucleotide is composed of three components: a sugar molecule (deoxyribose in DNA, ribose in RNA), a phosphate group, and a nitrogenous base.

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2
Q

What is the significance of the sequence of bases in a nucleic acid chain?

A

The sequence of bases along a nucleic acid chain carries genetic information. The specific order of the bases encodes the instructions for the synthesis of proteins and other cellular functions.

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3
Q

How does DNA replication occur?

A

DNA replication occurs through a process called semi-conservative replication. Each DNA strand serves as a template for the creation of a new complementary strand. The result is two identical DNA molecules, each containing one original strand and one newly synthesized strand.

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4
Q

How is protein synthesis related to DNA and RNA?

A

DNA itself is not directly involved in protein synthesis. Instead, DNA is transcribed into mRNA through a process called transcription. The mRNA molecules then serve as templates for protein synthesis

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5
Q

What is the role of messenger RNA (mRNA) in protein synthesis?

A

Messenger RNA (mRNA) is a type of RNA molecule that carries the genetic information from DNA to the cellular machinery responsible for protein synthesis. mRNA acts as an intermediary, conveying the instructions encoded in DNA to guide the synthesis of proteins.

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6
Q

What is the relationship between transcription and translation?

A

Transcription is the process where DNA is copied into mRNA, while translation is the process where mRNA is used as a template to synthesize proteins according to the genetic instructions encoded in the mRNA.

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7
Q

What is the genetic code, and what does it define?

A

The genetic code defines the relationship between the sequence of bases in DNA (or its mRNA transcript) and the sequence of amino acids in a protein. It is nearly the same in all organisms and consists of codons, which are sequences of three bases that specify a particular amino acid.

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8
Q

Why are naturally occurring DNA molecules long?

A

Naturally occurring DNA molecules are long because they need to carry the genetic information necessary for the functioning of organisms, even in the simplest ones

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9
Q

Can you provide examples of DNA lengths in different organisms?

A

Polyoma virus: Two intertwined strands, each 5100 nucleotides long.
E. coli: A single DNA molecule consisting of two chains, each with 4.6 million nucleotides.
Human genome: Approximately 3 billion nucleotides in each chain of DNA, divided among 23 distinct chromosomes of different sizes.
Indian muntjac: The genome is nearly as large as the human genome but distributed on only 3 chromosomes. The largest chromosome has two chains of over 1 billion nucleotides each.

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10
Q

How many nucleotides are present in each chain of the human genome?

A

Each chain of the human genome contains approximately 3 billion nucleotides.

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11
Q

What is the significance of codons in the genetic code?

A

Codons are sequences of three bases (nucleotides) in DNA or mRNA that code for specific amino acids or serve as start or stop signals in protein synthesis. The genetic code is degenerate, meaning that multiple codons can code for the same amino acid.

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12
Q

Can you explain the concept of gene expression and its relationship to DNA, RNA, and proteins?

A

Gene expression refers to the process by which information encoded in genes is used to create functional proteins or other cellular products. It involves the transcription of DNA into mRNA and the subsequent translation of mRNA into proteins. Gene expression is a fundamental process for the functioning and development of organisms.

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13
Q

What proteins are involved in DNA replication?

A

DNA polymerases, primase, DNA helicase, DNA ligase, single-stranded binding proteins, and various other proteins that assist in the initiation, elongation, and termination stages of replication

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14
Q

What is the role of DNA polymerases in DNA replication?

A

DNA polymerases play a crucial role in DNA replication. They promote the formation of bonds between individual units of the DNA molecule, called nucleotides, and add them step by step to build a new DNA chain.

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15
Q

What are the activated precursors required for DNA synthesis?

A

deoxynucleoside 5’-triphosphates (dATP, dGTP, dCTP, and TTP) along with the presence of magnesium ions (Mg2+).

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16
Q

How is the new DNA chain assembled during replication?

A

The new DNA chain is assembled directly on a preexisting DNA template. The DNA polymerases read the template DNA strand and add complementary nucleotides to the growing DNA chain, ensuring that the bases on the incoming nucleotides match the bases on the template strand.

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17
Q

What is the function of primase in DNA replication?

A

Primase is an enzyme involved in DNA replication that initiates the synthesis of RNA primers. These primers provide a starting point for DNA polymerases to begin synthesizing a new DNA strand.

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18
Q

How is the accuracy of DNA replication maintained?

A

The accuracy of DNA replication is maintained through a multilayered system. Accurate DNA synthesis itself has a certain error rate, but it is reduced by proofreading processes during DNA synthesis. Additionally, postreplication mismatch repair further reduces errors by detecting and correcting mistakes after replication.

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19
Q

What is the error rate required to replicate the human genome without mistakes?

A

To replicate the human genome without mistakes, an error rate of less than 1 error per 3x10^9 base pairs must be achieved.

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20
Q

What are the different layers of the system that ensure accurate DNA synthesis?

A

The system that ensures accurate DNA synthesis involves multiple layers. It includes accurate DNA synthesis itself, which has an error rate of approximately 1 error per 10^3 to 10^4 inserted bases. There are also proofreading mechanisms during DNA synthesis that reduce the error rate to about 1 error per 10^6 to 10^7 base pairs.
Furthermore, postreplication mismatch repair processes further reduce the error rate to around 1 error per 10^9 to 10^10 base pairs.

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21
Q

How does postreplication mismatch repair reduce the error rate in DNA replication?

A

Postreplication mismatch repair is a mechanism that detects and corrects errors after DNA replication. It helps reduce the error rate in DNA replication to approximately 1 error per 10^9 to 10^10 base pairs.

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22
Q

How does primase initiate synthesis without a primer, and what is its role in DNA replication?

A

Primase initiates synthesis without a primer by synthesizing a short RNA primer complementary to the DNA template. The RNA primer provides a starting point for DNA polymerases to bind and begin DNA synthesis.

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23
Q

How does the presence of magnesium ions (Mg2+) contribute to the DNA synthesis reaction?

A

Magnesium ions (Mg2+) play a crucial role in DNA synthesis. They stabilize the negatively charged phosphate groups of the dNTPs, facilitating the bonding reaction between the incoming nucleotide and the growing DNA chain. Mg2+ ions also help in the proper positioning of the dNTP within the active site of DNA polymerases.

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24
Q

What are the specific proofreading mechanisms employed by DNA polymerases during DNA synthesis?

A

DNA polymerases employ proofreading mechanisms to ensure accuracy during DNA synthesis. These mechanisms include exonuclease activity, where the polymerase can remove mismatched nucleotides from the growing DNA chain and replace them with the correct ones.

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25
Q

What are the specific functions of each protein in the DNA Replicase system or Replisomes?

A

DNA polymerases: Catalyze the synthesis of new DNA strands by adding nucleotides.
Primase: Initiates the synthesis of RNA primers.
DNA helicase: Unwinds the double-stranded DNA to create a replication fork.
DNA ligase: Joins the Okazaki fragments on the lagging strand during DNA replication.
Single-stranded binding proteins: Stabilize and protect the single-stranded DNA regions during replication.

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26
Q

How does the catalytic activity of DNA polymerases promote the formation of bonds in the DNA backbone?

A

DNA polymerases have an active site that can catalyze the formation of phosphodiester bonds between nucleotides. They use the energy from the incoming deoxynucleoside 5’-triphosphate (dNTP) to join the 3’-hydroxyl group of the growing DNA chain with the 5’-phosphate group of the incoming nucleotide, thereby forming the bond in the DNA backbone.

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27
Q

What’s the site of DNA replication

A

Replication fork
It is formed by the newly synthesized daughter helices and resembles a two-pronged fork.

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28
Q

How are the leading and lagging strands synthesized during DNA replication?

A

The leading strand is synthesized continuously during DNA replication, while the lagging strand is synthesized in small fragments called Okazaki fragments.

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29
Q

What is the direction of DNA synthesis by DNA polymerases?

A

DNA polymerases synthesize DNA in the 5’ to 3’ direction. They cannot synthesize DNA in the opposite direction (3’ to 5’).

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30
Q

How are Okazaki fragments joined together during replication?

A

together during replication by an enzyme called DNA ligase. DNA ligase catalyzes the formation of covalent bonds between the fragments, resulting in a continuous daughter strand.

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31
Q

What is the difference between the leading and lagging strands?

A

The leading strand is synthesized continuously in the same direction as the replication fork, while the lagging strand is synthesized discontinuously in the opposite direction. The leading strand is synthesized without interruption, while the lagging strand is synthesized in fragments.

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32
Q

How does the discontinuous assembly of the lagging strand

A

The discontinuous assembly of the lagging strand enables overall growth because the fragments are still synthesized in the 5’ to 3’ direction at the nucleotide level. When the fragments are joined together, they form a continuous strand.

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33
Q

What is the role of DNA ligase in DNA replication?

A

DNA ligase plays a crucial role in DNA replication by sealing breaks in double-stranded DNA molecules. It catalyzes the formation of phosphodiester bonds between the 3’-hydroxyl group of one DNA chain and the 5’-phosphoryl group of the other, resulting in the connection of DNA fragments.

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34
Q

What energy source drives the bond formation catalyzed by DNA ligase in different organisms?

A

ATP is typically used as the energy source, while in bacteria, NAD+ is commonly utilized.

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35
Q

What can DNA ligase seal in double-stranded DNA molecules?

A

DNA ligase can seal breaks in double-stranded DNA molecules. It is not able to link two molecules of single-stranded DNA or circularize single-stranded DNA. Its main function is to join the ends of DNA strands during replication or repair processes.

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36
Q

Can you explain the mechanism of DNA ligase in joining Okazaki fragments during DNA replication?

A

DNA ligase joins Okazaki fragments during DNA replication by catalyzing the formation of phosphodiester bonds between the adjacent fragments. It seals the nicks (unjoined ends) in the DNA backbone, resulting in the formation of a continuous daughter strand.

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37
Q

Can you explain the role of single-stranded binding proteins (SSBs) in DNA replication?

A

Single-stranded binding proteins (SSBs) stabilize and protect single-stranded DNA regions during DNA replication. They bind to the exposed single-stranded DNA, preventing it from forming secondary structures and being degraded by nucleases. SSBs also help to keep the DNA strands separated, allowing for efficient replication.

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38
Q

What are the functions of helicase in DNA replication, and how does it contribute to the unwinding of the DNA double helix?

A

Helicase plays a crucial role in DNA replication by unwinding the double-stranded DNA at the replication fork. It uses energy from ATP hydrolysis to break the hydrogen bonds between the base pairs, separating the DNA strands and creating the single-stranded DNA templates needed for DNA synthesis.

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39
Q

What is the function of topoisomerases in DNA replication, and how do they relieve torsional stress during replication?

A

Topoisomerases are enzymes involved in DNA replication that help relieve torsional stress and prevent DNA supercoiling. They achieve this by cutting and rejoining the DNA strands, allowing for controlled rotation of the DNA during replication.

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40
Q

What are topoisomerases and what role do they play in DNA processes?

A

Topoisomerases are enzymes that are involved in DNA processes such as replication, transcription, and recombination. They help regulate the degree of supercoiling in DNA, which is the twisting and winding of the DNA strands.

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41
Q

What is the difference between negative and positive supercoiling of DNA?

A

Negative supercoiling refers to the underwinding of DNA, which prepares it for processes like replication. Positive supercoiling, on the other hand, condenses DNA but makes strand separation more difficult.

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42
Q

How do Type I and Type II topoisomerases differ in their actions on DNA?

A

Type I topoisomerases cleave one strand of DNA and relax supercoiled DNA. Type II topoisomerases cleave both strands of DNA and utilize ATP energy to introduce negative supercoils into DNA.

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43
Q

What are some antibiotics that target bacterial topoisomerase II (DNA gyrase)?

A

Antibiotics such as novobiocin, nalidixic acid, and ciprofloxacin target bacterial topoisomerase II (DNA gyrase). Novobiocin blocks the binding of ATP to gyrase, while nalidixic acid and ciprofloxacin interfere with the breakage and rejoining of DNA chains.

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44
Q

How does camptothecin inhibit human topoisomerase I and what effect does it have on DNA?

A

Camptothecin inhibits human topoisomerase I by stabilizing the form of the enzyme covalently linked to DNA. This prevents DNA re-ligation and leads to DNA damage, ultimately causing apoptosis (programmed cell death).

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45
Q

What are autonomously replicating sequences (ARS) or replicators, and where have they been extensively studied?

A

Autonomously replicating sequences (ARS) or replicators are specific sequences in DNA that act as origins of replication. They have been extensively studied in eukaryotes, particularly in yeast

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46
Q

What is the function of the origin recognition complex (ORC) in initiating DNA replication?

A

The origin recognition complex (ORC) is a multisubunit protein complex that plays a crucial role in initiating DNA replication. It binds to several sequences within the replicator and helps recruit other proteins involved in replication.

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47
Q

How does the rate of replication fork movement differ between eukaryotes and E. coli?

A

The rate of replication fork movement in eukaryotes is slower compared to E. coli. Eukaryotes replicate at a rate of approximately 50 nucleotides per second, which is only one-twentieth of the rate observed in E. coli.

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48
Q

How long would it take to replicate an average human chromosome from a single origin at the rate observed in eukaryotes?

A

Replicating an average human chromosome from a single origin at the rate observed in eukaryotes (~50 nucleotides per second)

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49
Q

What are some potential applications or implications of understanding the mechanisms of topoisomerases and DNA replication?

A

Understanding the mechanisms of topoisomerases and DNA replication has several implications and applications. It helps in understanding genetic processes, developing antibiotics that target bacterial topoisomerases, studying diseases related to DNA replication errors, and exploring potential therapeutic strategies for cancer treatment. Additionally, knowledge of DNA replication is crucial for advancements in genetic engineering, biotechnology, and synthetic biology

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50
Q

What are the specific mechanisms by which Type I and Type II topoisomerases cleave and reseal DNA strands?

A

Type I topoisomerases cleave one strand of the DNA, forming a transient covalent bond between the enzyme and the DNA. The DNA strand is then passed through the break, and the enzyme reseals the nicked DNA strand.
Type II topoisomerases cleave both strands of the DNA, creating a double-stranded break. They form a covalent protein-DNA intermediate, allowing them to pass another segment of DNA through the break. Finally, the enzyme reseals the double-stranded break.

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51
Q

What are some of the key sequences recognized by the origin recognition complex (ORC) during DNA replication initiation in eukaryotes?

A

The origin recognition complex (ORC) recognizes specific sequences within the replicator during DNA replication initiation in eukaryotes. These sequences, known as origin recognition sites, vary among species but generally contain conserved DNA motifs that serve as binding sites for ORC.

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52
Q

How do different types of autonomously replicating sequences (ARS) or replicators function, and what factors determine their efficiency and specificity?

A

The slower rate of replication fork movement in eukaryotes compared to E. coli can be attributed to multiple factors, such as the larger size and complexity of eukaryotic genomes, the need for coordination with chromatin structure, and the requirement for more complex protein-protein interactions during replication.

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53
Q

What are the potential long-term consequences of DNA replication errors caused by topoisomerase dysfunction?

A

DNA replication errors caused by topoisomerase dysfunction can have various long-term consequences. They can lead to mutations, genomic instability, and the development of genetic diseases or predisposition to certain cancers. Additionally, errors in DNA replication can result in impaired cellular function and contribute to aging processes.

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54
Q

How does replication of human chromosomes occur?(direction)

A

Replication of human chromosomes occurs bidirectionally from multiple origins, with each origin initiating the replication process in both directions.

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55
Q

Why are multiple origins of replication necessary in eukaryotic cells?

A

Multiple origins of replication are necessary in eukaryotic cells because eukaryotic chromosomes are larger than bacterial chromosomes. Having multiple origins allows for simultaneous replication of different regions of the chromosome, making the replication process more efficient and faster.

56
Q

What are the different types of DNA polymerases found in eukaryotes?

A

DNA polymerases found in eukaryotes include α, β, γ, δ, and ɛ.

57
Q

Which DNA polymerase is responsible for chromosome replication in mammalian cells?

A

DNA polymerase α is responsible for chromosome replication in mammalian cells.

58
Q

What is the speed of polymerization of DNA polymerase α compared to bacterial enzymes?

A

The speed of polymerization of DNA polymerase α is slower compared to bacterial enzymes. It can polymerize about 100 nucleotides per second, whereas bacterial enzymes can polymerize about 10 times faster.

59
Q

What are the subunits of mammalian DNA polymerase α and what are their functions?

A

Mammalian DNA polymerase α consists of four subunits. One subunit has a primase activity, and the largest subunit (with a molecular weight of approximately 180,000) contains the polymerization activity.

60
Q

Why is DNA polymerase α not suitable for high-fidelity DNA replication?

A

DNA polymerase α lacks proofreading exonuclease activity, which means it cannot correct errors during DNA replication. This makes it unsuitable for high-fidelity DNA replication.

61
Q

What is the role of proliferating cell nuclear antigen (PCNA) in DNA replication?

A

Proliferating cell nuclear antigen (PCNA) is a protein that associates with DNA polymerase α and stimulates its activity during DNA replication.

62
Q

Which DNA polymerase is involved in extending the primers synthesized by DNA polymerase α? And it’s function

A

The primers synthesized by DNA polymerase α are extended by the multi-subunit DNA polymerase δ.
δ is the main enzyme responsible for synthesizing the lagging strand during DNA replication. It participates in both leading and lagging strand synthesis and possesses 3’ to 5’ exonuclease proofreading activity.

63
Q

What are the specific functions of DNA polymerases β, γ, and ɛ in mammalian cells?

A

DNA polymerase β is involved in DNA repair processes, DNA polymerase γ is responsible for mitochondrial DNA synthesis, and DNA polymerase ɛ is primarily used for leading strand synthesis.
It has high fidelity and proofreading capabilities. Pol ε also participates in DNA repair processes.

64
Q

In what situations does DNA polymerase ɛ replace DNA polymerase δ?

A

DNA polymerase ɛ can replace DNA polymerase δ in some situations, such as during DNA repair processes.

65
Q

How does DNA polymerase δ contribute to both leading and lagging strand synthesis?

A

DNA polymerase δ contributes to both leading and lagging strand synthesis in a complex comparable to the dimeric bacterial DNA polymerase III.

66
Q

How does the replication machinery in eukaryotes compare to that of bacteria?

A

The replication machinery in eukaryotes is similar to that of bacteria, but there are some differences due to the larger size and complexity of eukaryotic genomes.

67
Q

What are the differences between DNA polymerase α and DNA polymerase III in bacteria?

A

DNA polymerase α and DNA polymerase III in bacteria have different subunit compositions and functions, with DNA polymerase α being responsible for priming and DNA polymerase III being the main enzyme involved in DNA synthesis.

68
Q

Which DNA polymerase is involved in DNA repair processes?

A

DNA polymerase β is involved in DNA repair processes.

69
Q

What is the role of DNA polymerase γ in eukaryotic cells?

A

DNA polymerase γ is specifically involved in mitochondrial DNA synthesis.

70
Q

How does DNA polymerase δ proofread and correct errors during DNA synthesis?

A

DNA polymerase δ has a proofreading exonuclease activity, which allows it to remove mismatched nucleotides and correct errors during DNA synthesis.

71
Q

In mammalian cells, there are ____ DNA polymerases: namely

A

five
α, β, γ, δ, and ɛ.

72
Q

What’s the feature of DNA polymerase α

A

DNA polymerase α is the major enzyme responsible for chromosome replication but has lower speed and lacks proofreading activity.
DNA polymerase α synthesizes short primers for Okazaki fragments on the lagging & leading strand and is stimulated by proliferating cell nuclear antigen (PCNA).
Polymerase about 100 neuclotide per second (in bacteria is about×10)

73
Q

Features of DNA polymerase δ

A

DNA polymerase δ, which has proofreading activity, extends the primers synthesized by DNA polymerase α and carries out both leading and lagging strand synthesis.

74
Q

Features of DNA polymerase β, DNA polymerase γ, and DNA polymerase ɛ

A

DNA polymerase β is involved in DNA repair, DNA polymerase γ is responsible for mitochondrial DNA synthesis, and DNA polymerase ɛ is used for leading strand and may function at the replication fork, similar to bacterial DNA polymerase I, by removing the primers of Okazaki fragments on the lagging strand.

75
Q

DNA polymerase δ is replaced by DNA polymerase___ in certain situations, such as

A

DNA polymerase δ is replaced by DNA polymerase ɛ in certain situations, such as during DNA repair processes.

76
Q

______ is a compound that inhibits the DNA polymerase of the herpes simplex virus. And how

A

Acyclovir
It is phosphorylated by a virally encoded thymidine kinase and binds to the viral enzyme with high affinity.

77
Q

___ is used to treat herpes simplex

A

Acyclovir is a compound that was developed by a scientist named Gertrude Elion

78
Q

Acyclovir is made up of a molecule called _____, which is a building block of DNA, attached to an incomplete ____
. This structure allows acyclovir to be recognized and modified by a specific enzyme called _______ which is produced by the herpes virus.

A

guanine
ribose ring.
thymidine kinase,

79
Q

When acyclovir enters a virus-infected cell, the viral thymidine kinase enzyme attaches a phosphate group to it, forming a modified version called acyclo-GMP. This modified molecule is then further modified by cellular enzymes into acyclo-GTP.

A

Acyclo-GTP has a higher affinity or attraction to the viral thymidine kinase enzyme compared to the cellular thymidine kinase. This means that it mainly gets converted into acyclo-GTP in the virus-infected cells

80
Q

Acyclo-GTP acts in two ways to inhibit the herpes DNA polymerase. They are?

A

First, it competes with the normal building blocks of DNA, called nucleotides, when they try to bind to the DNA polymerase. This competition makes it difficult for the herpes DNA polymerase to continue replicating the viral DNA.
Second, acyclo-GTP lacks a specific chemical group called a 3’ hydroxyl, which is needed for adding more nucleotides to the growing DNA chain. Without this hydroxyl group, acyclo-GTP acts as a “chain terminator”

81
Q

After replication there’s a process called DNA methylation whats it

A

After DNA replication, there is a process called DNA methylation that occurs. This process involves adding a chemical modification called a methyl group to the DNA molecule at a specific position called C5 of cytosine.

82
Q

This methylation process is catalyzed or facilitated by an enzyme called

A

DNA methyltransferase (abbreviated as Dam).

83
Q

Whats Gene silencing

A

DNA methylation is a common mechanism associated with gene silencing, which means it turns off or reduces the activity of certain genes.

84
Q

Transcriptional regulation of tissue specific genes during cellular differentiation also results from

A

DNA methylation.

85
Q

Function of DNA methylation

A

DNA methylation helps regulate the activity of tissue-specific genes, ensuring that the right genes are expressed in the right cells at the right time.

86
Q

example is X-chromosomal inactivation, which happens in female mammals to balance the gene expression between the two X chromosomes. It also contributes to genomic imprinting, which is the selective silencing of either the maternal or paternal alleles (gene copies).

A
87
Q

Methylation occurs in

A

CG rich areas in the promoter region
The promoter region is a region of DNA near the beginning of a gene that helps control its expression or activity.

88
Q

The changes in gene expression that result from methylation can be passed down from one generation to another, but sometimes these inherited marks or imprints can be erased and rewritten during the process.

A
89
Q

Epigenetic information refers

A

to these inherited marks or modifications that can change how genes are expressed. They are often described as “writings with nature’s pencil”

90
Q

What’s ROS and how it affects methylation

A

Reactive oxygen species (ROS), which are molecules that can cause damage to cells
ROS can lead to a process called hypermethylation, which involves excessive methylation of certain areas of the DNA

91
Q

Methylation is influenced by factors such as

A

Methylation is influenced by factors like cancer, reactive oxygen species, cellular senescence, and can have implications for age-related diseases like type 2 diabetes

92
Q

Unrepaired DNA damage is known as a

A

lesion

93
Q

Most serious lesion is

A

change in base sequence of DNA
It could be replicated and become permanent

94
Q

What’s mutation

A

Mutation is the permanent change in DNA base sequence
It could be addition, substitutions or deletion

95
Q

What’s silent mutation

A

Silent mutation is when it affects non essential DNA or has negligible effect on gene function

96
Q

 In mammals accumulation of mutation is strongly correlated with .

A

cancer

97
Q

These DNA repair mechanisms are like a quality control system that ensures that only about 1 in every 1000 damaged DNA molecules becomes a permanent mutation or change in our genetic code.

A
98
Q

The replication process should be carried out with

A

High fidelity, otherwise the information is altered

99
Q

Stages of DNA repair

A

General repair
Proof reading
Exonucleolytic proof reading
Nucleotide Excision repair
Strand Directed Mismatch Repair

100
Q

What’s epigenome

A

The epigenome refers to the chemical modifications and proteins that can control the activity of genes without changing the underlying DNA sequence.

101
Q

Deregulation of epigenome has been recognized as a fundamental mechanism of carcinogenesi

A
102
Q

Hypermethylation of CG islands have been observed to silence

A

oncosuppressor genes. Stuffs that can prevent cancer

103
Q

Another type of deregulation involves changes in histone modifications, specifically _____&______

A

acetylation and methylation

104
Q

What are histones

A

Histones are proteins that help package and organize DNA in the nucleus of cells

105
Q

Inhibition of epigenetic regulators like ____&_____ are being looked upon as potential target for chemotherapy

A

DNA methyl transferase (DMT) and histone decaetylase
(HDAC)

106
Q

What’s exonucleolytic proofreading
What’s Exonucleases

A

mechanism ensures that mistakes in DNA replication, such as incorrect base pairing, are detected and corrected promptly.
DNA polymerase possesses a specific activity called 3’ to 5’ exonuclease activity. Exonucleases are enzymes that can remove nucleotides from the ends of DNA strands.

107
Q

_______ is a mechanism that cells use to prevent unwanted mutations in DNA caused by UV radiation

A

Nucleotide Excision Repair (NER)

108
Q

Eg of mutations caused by UV radiation is?

A

Thymine dimers are abnormal formations of two adjacent thymine bases in the DNA strand that can occur due to UV exposure.

109
Q

There are___major proteins involved in NER in mammalian cells

A

9
XPA, XPB, XPC, XPD, XPE, XPF, and XPG.
their names are based on the diseases associated with deficiencies in those proteins

110
Q

The names of NER is derived from

A

These names are derived from a genetic disorder called xeroderma pigmentosum, which is characterized by extreme sensitivity to UV radiation and a high risk of skin cancer.

111
Q

NER occurs alongside the replication process, ensuring the accurate repair of damaged DNA and reducing the risk of mutations.

A
112
Q

CSA and CSB are enzymes that are deficient in another genetic disorder called ____, which is associated with developmental and neurological abnormalities

A

Cockayne syndrome

113
Q

The original template DNA strand contains certain methylated residues, specifically

A

N6-methyl adenine and 5-methyl cytosine.

114
Q

while the newly synthesized DNA strand may initially be free of methylation, it can acquire methyl groups from the original template strand or undergo dynamic changes in methylation patterns during replication and other cellular processes.

A
115
Q

The wrong base is removed by the endonuclease activity of the ___
It removes _____to_____ nucleotides around the wrong base

A

XPG
24-32 nucleotides

116
Q

What’s Strand Directed Mismatch Repair
The detection & looping of E coli is removed by

A

When a miss match or mistake I identified a loop is made and the segment is removed
And correct one is added by ligase and SSB’s

MutS, MutC, MutH

117
Q

What’s Base Excision repair

A

Base Excision repair is the process by which cells fixes depurination damage
Depurination causes certain bases in DNA, specifically cytosine, adenine, and guanine, to change into different bases called uracil, hypoxanthine, and xanthine, respectively.

118
Q

How does Base Excision repair fix depurination

A

enzymes called N-glycosylases that can remove these abnormal bases from the DNA molecule. After the abnormal base is removed, there is a gap in the DNA where the sugar molecule used to be. To fill in this gap, another enzyme called apurinic endonuclease removes the sugar. Then, a repair DNA polymerase (DNAP) comes in and adds the correct base to fill the gap. Finally, a ligase enzyme seals the DNA strand back together.

119
Q

What’s Xeroderma Pigmentosum (XP)

A

is an inherited disease that affects the skin.

120
Q

XP is caused by
And there are_____ XP genes

A

defects in the nucleotide excision repair (NER) mechanism, which is responsible for fixing DNA damage.
There are seven XP genes (A to G) involved in the NER mechanism.

Mutations in any one of these XP genes can lead to the development of XP.

Exposure to ultraviolet (UV) light, particularly sunlight, can cause the formation of thymine dimers in the DNA.

In XP patients, the repair mechanism is impaired, and these mutations accumulate, increasing the risk of cancer.

121
Q

XP patients are highly sensitive to UV rays and may experience skin problems like blisters when exposed to sunlight.
Avoiding sunlight and using sunscreen can be beneficial for XP patients.
XP patients have a significantly higher risk of developing skin cancer compared to normal individuals (1000-fold greater risk).

A
122
Q

XP is a genetic disease that affects the skin and is inherited in

A

an autosomal recessive manner.

123
Q

It is possible to diagnose XP before birth through

A

prenatal testing.

124
Q

What’s Ataxia Telangiectasia (AT)

A

Ataxia Telangiectasia (AT) is a genetic disease that’s caused by a change in a specific gene called ataxia telangiectasia mutated (ATM), which is found on chromosome 11q.

125
Q

What are the symptoms of Ataxia Telangiectasia

A

People with AT have an increased sensitivity to UV light, making their skin more prone to damage from the sun.
Cerebellar ataxia is a common symptom of AT, causing problems with balance and coordination.
Telangiectasia refers to small blood vessels that can be seen in the eyes and skin of individuals with AT.
People with AT have a higher risk of developing lympho-reticular neoplasms, which are cancers affecting the lymph nodes and immune system.

126
Q

AT affects approximately

A

1 in every 40,000 individuals.

127
Q

Replication is ________, each strand acting as template for a new daughter strand.

A

semiconservative

128
Q

Replication is carried out in three identifiable phases:

A

initiation, elongation, and termination

129
Q

The reaction starts at the origin and usually proceeds bidirectionally meaning

A

The reaction starts at the origin and usually proceeds bidirectionally.

DNA is synthesized in the 5’ to 3’ direction by DNA polymerases.

130
Q

The fidelity of DNA replication is maintained by (

A

1) base selection by the polymerase, (2) a
3’to 5’proofreading exonuclease activity that is part of most DNA polymerases,
(3)
specific repair systems for mismatches left behind after replication.

131
Q

DNA synthesis is done 5to 3 and proff reading is done 3 to5

A
132
Q

In E. coli, DNA polymerase _____ is the primary
replication enzyme.

A

III

133
Q

DNA polymerase 1 aid in replication, recombination and repair by?

A

DNA polymerase I synthesizes DNA in the 5’ to 3’ direction during replication.
It has a 3’ to 5’ exonuclease activity for proofreading and removing mismatched nucleotides.
The enzyme also exhibits a 5’ to 3’ exonuclease activity involved in nick translation during repair and recombination.
DNA polymerase I removes RNA primers synthesized by primase during replication and fills in the resulting gaps with DNA.
It plays a role in DNA repair, specifically base excision repair (BER), by filling in single-stranded gaps left after damaged bases are excised

134
Q

What’s Fanconi’s Anemia:

A

This condition is associated with defects in specific genes located on chromosomes 20q and 9q. It affects the repair of DNA cross-links, which can lead to an increased occurrence of cancer.

135
Q

What’s Bloom’s Syndrome: Bloom’s Syndrome

A

is caused by a gene located on chromosome 15q. It involves defects in DNA ligase or helicase, which are enzymes involved in DNA repair. Individuals with Bloom’s Syndrome have a higher risk of developing lymphoreticular malignancies.

136
Q

What’s Cockayne Syndrome:

A

Cockayne Syndrome is characterized by a defect in the NER mechanism, similar to XP. In this case, a specific transcription factor called TFIIH is defective. This condition is associated with stunted growth and mental retardation.

137
Q

What’s Hereditary Polyposis Colon Cancer (Lynch syndrome):

A

Lynch syndrome is caused by a defective gene on chromosome 2. The defect affects hMSH1 and hMSH2 genes, which are involved in mismatch repair. Individuals with Lynch syndrome have a higher risk of developing colon cancer due to problems in DNA repair.