Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Leading and Lagging Strands Prepare a table that lists the names and compares the functions of the precursors, enzymes, and other proteins needed to make the leading strand versus the lagging strand during DNA replication in \(E\). coli.

Short Answer

Expert verified
The leading strand is synthesized continuously with few RNA primers, while the lagging strand forms Okazaki fragments needing multiple primers and ligase to join fragments.

Step by step solution

01

Identify the Purpose of the Exercise

The task requires us to create a table comparing the leading and lagging strands during DNA replication in \( E. coli \). We need to list and compare the precursors, enzymes, and other proteins involved for each strand.
02

Understand DNA Replication Process

During DNA replication, the double-stranded DNA is unwound to create two single strands, which serve as templates for new strands. These templates are the leading and lagging strands, which replicate differently due to their orientation.
03

Define the Leading Strand Components

In the leading strand, DNA replication occurs continuously towards the replication fork. Key components include: a DNA template strand, DNA polymerase III for synthesizing DNA, and a primer synthesized by primase.
04

Define the Lagging Strand Components

In the lagging strand, replication occurs discontinuously away from the replication fork, forming Okazaki fragments. Important components include: multiple RNA primers made by primase, DNA polymerase III for fragment synthesis, and DNA ligase for joining fragments.
05

Compare and Compile Information into a Table

Create a table with two columns labeled "Leading Strand" and "Lagging Strand." List and compare the components such as DNA templates, DNA polymerases, primers, primase, Okazaki fragments, and DNA ligase usage in each column. Highlight that the leading strand is synthesized continuously, while the lagging strand is synthesized in fragments.
06

Review and Present the Table

Verify the table for accuracy in portrayal of the DNA replication process in \( E. coli \). Ensure that all key components and differences such as continuous vs. discontinuous synthesis are clearly described.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

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

Leading Strand
The leading strand is synthesized continuously during DNA replication. This strand is oriented in the 5' to 3' direction toward the replication fork. This means it can be replicated in one continuous motion as the DNA unwinds.
Some key points about the leading strand include:
  • Replication occurs in the same direction as the movement of the replication fork.
  • DNA polymerase III is the enzyme responsible for adding nucleotides to the growing DNA chain.
  • The process requires an initial RNA primer, synthesized by the enzyme primase, to provide a starting point for DNA polymerase III.
The leading strand provides a seamless, ongoing template facilitating efficient replication. This efficiency is a primary reason why DNA replication is as fast as it is in organisms like E. coli.
Lagging Strand
In contrast, the lagging strand is synthesized discontinuously. It goes in the opposite direction of the unwinding double helix, which is 3' to 5'. This results in a more complex, stop-and-start synthesis process.
Important aspects of the lagging strand include:
  • Its synthesis occurs in short segments called Okazaki fragments.
  • Each fragment starts with an RNA primer provided by primase.
  • DNA polymerase III then extends these primers, adding DNA nucleotides to synthesize each fragment.
  • Finally, DNA ligase connects the Okazaki fragments to form a continuous DNA strand.
Understanding this intricacy reveals why DNA replication needs to be meticulously coordinated, as each step relies on specific enzymes and timing.
E. coli Replication
E. coli serves as a model organism for studying DNA replication due to its relatively simple and efficient replication process. This bacterium's replication is both rapid and precise, making it an ideal subject for understanding basic genetic mechanisms.
Some noteworthy points about E. coli replication include:
  • The process is initiated at a specific location on the DNA molecule called the origin of replication.
  • It's remarkably fast, allowing the cell to replicate every 20 to 30 minutes under optimal conditions.
  • Efficient replication mechanisms help maintain genetic fidelity across generations in bacteria.
The balance between the leading and lagging strand synthesis is crucial for the high-speed and low-error rate of E. coli replication, emphasizing the intricate coordination involved in DNA replication.
Okazaki Fragments
Okazaki fragments are short sequences of DNA nucleotides, synthesized discontinuously on the lagging strand. These fragments are essential for lagging strand replication because the DNA polymerase can only add nucleotides in the 5' to 3' direction.
A few critical details about Okazaki fragments:
  • Each fragment begins with a small RNA primer, which is eventually replaced with DNA.
  • Multiple Okazaki fragments are synthesized simultaneously as the lagging strand is copied.
  • DNA ligase is responsible for joining these fragments into a cohesive DNA strand.
Okazaki fragments highlight the elegance and complexity of the DNA replication process, ensuring that even the lagging strand is accurately and efficiently replicated.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

DNA Replication Kornberg and his colleagues incubated soluble extracts of \(E\). coli with a mixture of dATP, dTTP, dGTP, and dCTP, all labeled with \({ }^{32} \mathrm{P}\) in the \(a\)-phosphate group. After a time, they treated the incubation mixture with trichloroacetic acid, which precipitates the DNA but not the nucleotide precursors. They then collected the precipitate and determined the extent of precursor incorporation into DNA from the amount of radioactivity present in the precipitate. a. If any one of the four nucleotide precursors were omitted from the incubation mixture, would radioactivity be found in the precipitate? Explain. b. Would \({ }^{32} \mathrm{P}\) be incorporated into the DNA if only dTTP were labeled? Explain. c. Would radioactivity be found in the precipitate if \({ }^{32} \mathrm{P}\) labeled the \(\beta\) phosphate or \(\gamma\) phosphate rather than the \(a\) phosphate of the deoxyribonucleotides? Explain.

The Ames Test In a nutrient medium that lacks histidine, a thin layer of agar containing \(\sim 10^{9}\) Salmonella typhimurium histidine auxotrophs (mutant cells that require histidine to survive) produces \(\sim 13\) colonies over a two-day incubation period at \(37^{\circ} \mathrm{C}\) (see Eig \(25-19\) ). How do these colonies arise in the absence of histidine? When investigators repeat the experiment in the presence of \(0.4 \mu \mathrm{g}\) of 2 -aminoanthracene, the number of colonies produced over two days exceeds 10,000 . What does this indicate about 2-aminoanthracene? What can you surmise about its carcinogenicity?

Strand Invasion in Recombination A key step in many homologous recombination reactions is strand invasion (see step 2 in Fig. 25-29). In almost every case, strand invasion proceeds with a single strand that has a free \(3^{\prime}\) end rather than a \(5^{\prime}\) end. What DNA metabolic advantage is inherent with the use of a free 3 ' end for strand invasion?

DNA Repair and Cancer Many pharmaceuticals used for tumor chemotherapy are DNA damaging agents. What is the rationale behind actively damaging DNA to address tumors? Why do such treatments often have a greater effect on a tumor than on healthy tissue?

The Chemistry of DNA Replication All DNA polymerases synthesize new DNA strands in the \(5^{\prime} \rightarrow 3^{\prime}\) direction. In some respects, replication of the antiparallel strands of duplex DNA would be simpler if there were also a second type of polymerase, one that synthesized DNA in the \(3^{\prime} \rightarrow 5^{\prime}\) direction. The two types of polymerase could, in principle, coordinate DNA synthesis without the complicated mechanics required for lagging strand replication. However, no such \(3^{\prime} \rightarrow 5^{\prime}\)-synthesizing enzyme has been found. Suggest two possible mechanisms for \(3^{\prime} \rightarrow 5^{\prime}\) DNA synthesis. Pyrophosphate should be one product of both proposed reactions. Could one or both mechanisms be supported in a cell? Why or why not? (Hint: You may suggest the use of DNA precursors not actually present in extant cells.)

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free