Homologous recombination in \(E .\) coli leads to the formation of regions of heteroduplex DNA. By definition, such regions contain mismatched bases. Why doesn't the mismatch repair system of \(E .\) coli eliminate these mismatches?

Short Answer

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The mismatch repair system of E. coli doesn't eliminate the mismatches in the heteroduplex DNA because during homologous recombination, the resulting heteroduplex regions contain DNA from two different parental molecules, both of which are fully methylated. The mismatch repair system cannot distinguish which strand to correct since both strands appear to the system to be 'correct'.

Step by step solution

01

Understanding Homologous Recombination

Homologous recombination is a type of genetic recombination in which nucleotide sequences are exchanged between two similar or identical molecules of DNA. In E. coli, this process generates regions of heteroduplex DNA.
02

Understanding Heteroduplex DNA

Heteroduplex DNA is DNA consisting of two strands, each of which is from a different one of two homologous chromosomes. It is formed during recombination and can contain mismatched bases.
03

Understanding Mismatch Repair System

The mismatch repair system is a system for recognizing and repairing erroneous insertion, deletion and mis-incorporation of bases that can arise during DNA replication and recombination. It ensures the fidelity of replication.
04

Why Mismatches Are Not Corrected by Mismatch Repair System

Specifically in the context of E. coli, the mismatch correction system works preferentially on newly synthesized (daughter) DNA strands, can distinguish between original (mother) and newly synthesized strands based on the degree of methylated adenine. Immediately after replication, the daughter strand is not yet fully methylated. Hence, the mismatch repair system can detect which strand contains the error. However, the regions of heteroduplex DNA formed during recombination contain strands from two different parental DNA molecules, and so both are fully methylated. Therefore, the repair system has no way of knowing which strand contains the 'correct' sequence and which strand contains the 'error', thus the mismatches in these regions are not repaired.

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Key Concepts

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

Heteroduplex DNA
During the fascinating dance of genetic recombination, a special form of DNA known as heteroduplex DNA arises. Picture this: two DNA helices, each from different parents, intertwine and swap segments, resulting in a hybrid molecule. This molecule is a heteroduplex because it's composed of two different, yet related, DNA strands.

Imagine a zipper joining two mismatched pieces of fabric, and you'll have a vivid metaphor for heteroduplex DNA. Occurring naturally during processes such as meiosis or in microbes like E. coli during homologous recombination, heteroduplex DNA may contain base pairs that do not match – these are the mismatches that can create diversity, but also potential errors.

For students grappling with this concept, consider heteroduplex DNA as an intermediate step toward genetic variation. It is the proof that life's genetic code is nimble, able to adapt and evolve through complex molecular shuffles.
Mismatch Repair System
The mismatch repair system is a crucial proofreading mechanism, which ensures that our genetic information is copied accurately. It's like an eagle-eyed editor scanning a manuscript for typos after the first draft (the DNA replication) is finished.

This system diligently corrects mispaired bases that sneak past the initial replication process. Without it, we'd accumulate errors faster than a faulty calculator, potentially leading to dire consequences like cancer. In E. coli, this system is quite sophisticated; it distinguishes between the old and new strands based on methylation patterns.

Understanding the Methylation Cue

Here's a crucial point for students: in E. coli, immediately after DNA replication, the parental strand is methylated, while the daughter strand is not. This difference guides the mismatch repair enzymes to the newly synthesized strand, where errors are most likely to occur. This nuanced mechanism showcases the ingenuity of our cellular processes and their role in safeguarding our genetic integrity.
Genetic Recombination
Genetic recombination is nature's way of shuffling the genetic deck. It adds variety to the biological game by allowing genes from different chromosomes to mix and match, creating unique combinations. This process not only generates diversity within a population but also drives evolution and adaptation.

In organisms like E. coli, this exchange occurs through precise mechanisms, ensuring that despite the reshuffling, vital genomic information remains intact. For students, think of genetic recombination as a careful exchange of genetic gifts between neighboring DNA molecules, fostering the emergence of new traits while preserving essential functions.

Homologous Versus Non-Homologous Recombination

Within the broader category of genetic recombination, homologous recombination deals with the exchange between sequences that are similar or identical. This partner dance ensures that the genetic information can blend without creating chaos, a stark contrast to the more unpredictable non-homologous recombination.
DNA Replication Fidelity
DNA replication fidelity is the precision with which our genetic code is copied during cell division. Think of it as a meticulous scribe who must transcribe an ancient text without introducing errors. This level of accuracy is critical; even the smallest mistake could result in malfunctioning proteins or even disease.

The replication machinery, including various enzymes like DNA polymerases, has evolved to perform this task with remarkable exactitude. It incorporates the correct nucleotides, proofreads each addition, and calls upon the mismatch repair system to fix any errors that escape the initial screening.

For students, it's essential to understand that while near-perfect, the system isn't infallible. Occasional slips lead to mutations, which can be harmful, beneficial, or neutral. This delicate balance between fidelity and mutation drives the diversity of life and enables species to adapt over time, highlighting how precision and slight imperfection work hand in hand within the biological world.

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Most popular questions from this chapter

If \(^{15} \mathrm{N}\) -labeled \(E .\) coli DNA has a density of \(1.724 \mathrm{g} / \mathrm{mL},^{14} \mathrm{N}\) -labeled DNA has a density of \(1.710 \mathrm{g} / \mathrm{mL}\), and \(E\). coli cells grown for many generations on \(^{14} \mathrm{NH}_{4}^{+}\) as a nitrogen source are transferred to media containing \(^{15} \mathrm{NH}_{4}^{+}\) as the sole N source, (a) what will be the density of the DNA after one generation, assuming replication is semiconservative? (b) Supposing replication took place by a dispersive mechanism, what would be the density of DNA after one generation? (c) Design an experiment to distinguish between semiconservative and dispersive modes of replication.

How do DNA gyrases and helicases differ in their respective functions and modes of action?

Asako Furukohri, Myron F. Goodman, and Hisaji Maki wanted to discover how the translesion DNA polymerase IV takes over from DNA polymerase III at a stalled replication fork (see Journal of Biological Chemistry \(283: 11260-11269,2008\) ). They showed that DNA polymerase IV could displace DNA polymerase III from a stalled replication fork formed in an in vitro system containing DNA, DNA polymerase III, the \(\beta\) -clamp, and SSB. Devise your own experiment to show how such displacement might be demonstrated. (Hint: Assume that you have protein identification tools that allow you to distinguish easily between DNA polymerase III and DNA polymerase IV.

Transposons are mutagenic agents. Why?

(a) What are the respective roles of the 5 '-exonuclease and \(3^{\prime}\) exonuclease activities of DNA polymerase I? (b) What might be a feature of an \(E .\) coli strain that lacked DNA polymerase I 3 '-exonuclease activity?

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