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Explain why half of DNA is replicated in a discontinuous fashion. a. Replication of the lagging strand occurs in the direction away from the replication fork in short stretches of DNA, since access to the DNA is always from the 5’ end. This results in pieces of DNA being replicated in a discontinuous fashion. b. Replication of the leading strand occurs in the direction away from the replication fork in short stretches of DNA, since access to the DNA is always from the 5’ end. This results in pieces of DNA being replicated in a discontinuous fashion. c. Replication of the lagging strand occurs in the direction of the replication fork in short stretches of DNA, since access to the DNA is always from the 5’ end. This results in pieces of DNA being replicated in a discontinuous fashion. d. Replication of the lagging strand occurs in the direction away from the replication fork in short stretches of DNA, since access to the DNA is always from the 3’ end. This results in pieces of DNA being replicated in a discontinuous fashion.

Short Answer

Expert verified
Option a.

Step by step solution

01

Understand DNA Replication

DNA replication involves unwinding the double helix and synthesizing new strands from each of the original strands. Each new strand is built in the 5’ to 3’ direction.
02

Leading and Lagging Strands

The leading strand is synthesized continuously in the direction of the replication fork (5' to 3'). The lagging strand, however, is synthesized in short stretches in the direction away from the replication fork.
03

Directionality Constraints

DNA polymerase can only add nucleotides to the 3' end of a primer. This means that replication on the lagging strand must happen in short, discontinuous segments known as Okazaki fragments, because the polymerase has to work away from the replication fork.
04

Identify the Correct Answer

Option a. correctly states that replication of the lagging strand occurs in the direction away from the replication fork in short stretches of DNA, since access to the DNA is always from the 5’ end. This results in DNA being replicated discontinuously.

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Key Concepts

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

lagging strand
In the process of DNA replication, the lagging strand is synthesized discontinuously. This is because DNA polymerase can only add new nucleotides in a 5’ to 3’ direction. The replication fork unwinds the DNA, separating the strands. The lagging strand must elongate away from the replication fork. Therefore, it is built in short segments called Okazaki fragments. These fragments are later connected by the enzyme DNA ligase to create a continuous strand.

Here are key points to remember about the lagging strand:
  • It is synthesized discontinuously in short sections known as Okazaki fragments.
  • The replication process moves away from the replication fork.
  • DNA ligase is needed to join the Okazaki fragments together.
  • It replicates in a 5' to 3' direction, but opposite to the unwinding direction of the fork.
leading strand
Unlike the lagging strand, the leading strand is synthesized continuously during DNA replication. It grows in the same direction as the replication fork, which allows it to be made in one continuous piece. This continuous synthesis makes it much simpler compared to the lagging strand, which is built in fragments.

Some important details about the leading strand include:
  • It is synthesized in a continuous manner.
  • The direction of synthesis is the same as the movement of the replication fork.
  • Like the lagging strand, it also extends in a 5’ to 3’ direction.

Since the template strand for the leading strand runs in a 3' to 5' direction, DNA polymerase can function smoothly without interruptions.
Okazaki fragments
Okazaki fragments are short sequences of DNA nucleotides which are synthesized discontinuously. They occur on the lagging strand during DNA replication. These fragments are essential because DNA polymerase can only synthesize new DNA in a 5’ to 3’ direction. During replication:
  • The lagging strand template, which reads from 3’ to 5’, necessitates the creation of these fragments.
  • RNA primers provide starting points for DNA polymerase to begin synthesis of each fragment.
  • Once multiple Okazaki fragments are synthesized, they are joined together by DNA ligase to form a continuous strand.

By filling in the gaps between individual fragments, the replication machinery ensures that the lagging strand is accurately copied and completed in a fragmented yet effective manner.

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Most popular questions from this chapter

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.

Explain why patients with Xeroderma Pigmentosa are more prone to cancer than the rest of the population a. Xeroderma Pigmentosa patients cannot employ the nucleotide excision repair mechanism. When these patients are exposed to UV light, thymine dimers are formed and they are not able to repair this defect. These dimers distort the structure of DNA and cause them to have a high risk of contracting skin cancer. b. Xeroderma Pigmentosa patients can employ the nucleotide excision repair mechanism. When these patients are exposed to UV light, the thymine dimers are formed and they are able to repair this defect. These dimers do not distort the structure of DNA and they have moderate risk of contracting skin cancer. c. Xeroderma Pigmentosa patients cannot employ the nucleotide excision repair mechanism. When these patients are exposed to UV light, the adjacent adenine forms dimers and they are not able to repair this defect. These dimers distort the structure of DNA and they have high risk of contracting skin cancer. d. Xeroderma Pigmentosa patients cannot employ the nucleotide excision repair mechanism. When these patients are exposed to UV light, the adjacent thymine cannot form thymine dimers and they are not able to repair this defect. The non-formation of dimers distorts the structure of DNA and they have high risk of contracting skin cancer.

Discuss the effects of point mutations on a DNA strand. a. Mutations can cause a single change in an amino acid. A nonsense mutation can stop the replication or reading of that strand. Insertion or deletion mutations can cause a frame shift. This can result in non-functional proteins. b. Mutations can cause a single change in amino acid. A missense mutation can stop the replication or reading of that strand. Insertion or deletion mutations can cause a frame shift. This can result in non-functional proteins. c. Mutations can cause a single change in amino acid. A nonsense mutation can stop the replication or reading of that strand. Substitution mutations can cause a frame shift. This can result in non-functional proteins. d. Mutations can cause a single change in amino acid. A nonsense mutation can stop the replication or reading of that strand. Insertion or deletion mutations can cause a frame shift. This can result in functional proteins.

Compare and contrast the similarities and differences between eukaryotic and prokaryotic DNA. a. Eukaryotes have a single, circular chromosome, while prokaryotes have multiple, linear chromosomes. Prokaryotes pack their chromosomes by super coiling, managed by DNA gyrase. Eukaryote chromosomes are wrapped around histone proteins that create heterochromatin and euchromatin, which is not present in prokaryotes. b. Prokaryotes have a single, circular chromosome, while eukaryotes have multiple, linear chromosomes. Prokaryotes pack their chromosomes by super coiling, managed by DNA gyrase. Eukaryote chromosomes are wrapped around histone proteins that could form heterochromatin, which is not present in prokaryotes. c. Prokaryotes have a single, circular chromosome, while eukaryotes have multiple, linear chromosomes. Eukaryotes pack their chromosomes by super coiling, managed by DNA gyrase. Prokaryotes chromosomes are wrapped around histone proteins that could form heterochromatin, which is not present in eukaryotes. d. Prokaryotes have a single, circular chromosome, while eukaryotes have multiple, linear chromosomes. Prokaryotes pack their chromosomes by super coiling, managed by DNA gyrase. Eukaryote chromosomes are wrapped around histone proteins that could form heterochromatin, which is present in prokaryotes.

Explain how the components of DNA fit together. a. DNA is composed of nucleotides, consisting of a 5 carbon sugar, a phosphate, and a nitrogenous base. DNA is a double helical structure in which complementary base pairing occurs. Adenine pairs with thymine and guanine pairs with cytosine. Adenine and thymine form two hydrogen bonds and cytosine and guanine form three hydrogen bonds. The two individual strands of DNA are held together by covalent bonds between the phosphate of one nucleotide and sugar of the next. The two strands run anti parallel to each other. b. DNA is composed of nucleotides, consisting of a 5 carbon sugar, a phosphate, and a nitrogenous base. DNA is a double helical structure in which complementary base pairing occurs. Adenine pairs with cytosine and guanine pairs with thymine. Adenine and cytosine form two hydrogen bonds and guanine and thymine form three hydrogen bonds. The two individual strands of DNA are held together by covalent bonds between the phosphate of one nucleotide and sugar of the next. The two strands run anti parallel to each other. c. DNA is composed of nucleotides, consisting of a 5 carbon sugar, a phosphate, and a nitrogenous base. DNA is a double helical structure in which complementary base pairing occurs. Adenine pairs with cytosine and guanine pairs with thymine. Adenine and cytosine form three hydrogen bonds and guanine and thymine form two hydrogen bonds. The two individual strands of DNA are held together by covalent bonds between the phosphate of one nucleotide and sugar of the next. The two strands run antiparallel to each other. d. DNA is composed of nucleotides, consisting of a 5 carbon sugar, a phosphate, and a nitrogenous base. DNA is a double helical structure in which complementary base pairing occurs. Adenine pairs with cytosine and guanine pairs with thymine. Adenine and cytosine form three hydrogen bonds and guanine and thymine form two hydrogen bonds. The two individual strands of DNA are held together by covalent bonds between the phosphate of one nucleotide and sugar of the next. The two strands run parallel to each other.

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