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Chapter 5: Problem 89

What is a mutation? List and briefly explain the two major classes of mutations.

Short Answer

Expert verified
A mutation is a change in the DNA sequence of an organism that can result from errors during DNA replication or exposure to external factors. There are two major classes of mutations: gene mutations and chromosomal mutations. Gene mutations occur within a single gene and include point mutations (changes in a single nucleotide) and frameshift mutations (insertion or deletion of nucleotides that shifts the reading frame). Chromosomal mutations affect the structure or number of chromosomes and include deletions, duplications, inversions, translocations, and aneuploidy.

Step by step solution

01

Definition of Mutation

A mutation is a change in the DNA sequence of an organism, either through errors during DNA replication or as a result of exposure to certain external factors, such as chemicals or radiation. Mutations can have various effects on the organism's traits and often play an essential role in evolution.
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Major Class of Mutation 1: Gene Mutations

Gene mutations take place on a small scale within the DNA sequence of a single gene. They can occur in two ways: point mutations and frameshift mutations. 1. Point mutations: These mutations involve changes to a single nucleotide, or DNA building block, in the gene. There are three types of point mutations: silent mutations, which do not affect the protein produced; missense mutations, which changes one amino acid in the protein, potentially altering its function; and nonsense mutations, which create a premature stop codon in the mRNA leading to a truncated, usually nonfunctional protein. 2. Frameshift mutations: These mutations occur when one or more nucleotides are inserted or deleted from the DNA sequence, causing the reading frame of the genetic code to shift. The result of a frameshift mutation is typically a nonfunctional protein, as every amino acid downstream of the mutation site is changed.
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Major Class of Mutation 2: Chromosomal Mutations

Chromosomal mutations affect the structure or number of chromosomes in a cell. These mutations can happen during cell division, through errors in chromosome replication, or as a result of exposure to mutagens. There are several types of chromosomal mutations, including: 1. Deletion: A section of the chromosome is lost, potentially leading to the loss of one or more genes. 2. Duplication: A section of the chromosome is duplicated, resulting in extra copies of some genes. 3. Inversion: A section of the chromosome is reversed, leading to the alteration of gene order. 4. Translocation: A section of the chromosome is relocated to a different chromosome, causing the disruption of gene function. 5. Aneuploidy: An organism has an abnormal number of chromosomes, often due to errors during cell division.

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Key Concepts

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

Gene Mutations
Gene mutations are alterations in the DNA sequence that impact just a single gene. These changes can mess with the instructions used to make proteins, which can sometimes cause problems for the organism. Gene mutations mainly happen in two forms: point mutations and frameshift mutations.

These mutations are small-scale and only concern the sequence of nucleotides in a particular gene. This means that while their scope is limited, the effects can be significant if the affected gene serves a crucial function. Gene mutations are an essential concept in genetics because they illustrate how small DNA sequence changes can trigger big effects.
Chromosomal Mutations
Chromosomal mutations involve a bigger chunk of DNA and consequently, have a wider impact. These mutations either disrupt the structure or alter the number of entire chromosomes within a cell.

There are several ongoing ways they occur, such as through deletions or duplications of sections of the chromosome, inversions, translocations, or even changes in the number of chromosomes themselves (aneuploidy). Such mutations can cause major issues, including genetic disorders.
  • Deletion can cause the loss of vital genes.
  • Duplications might result in excess production of certain proteins.
  • Inversions can cause rearrangements within genes, possibly mucking up their functions.
Though chromosomal mutations are rarer than gene mutations, their consequences on the organism tend to be more profound, often influencing multiple traits.
DNA Sequence Changes
DNA sequence changes are the basis of mutations. These changes can occur naturally during cell division but might also result from environmental factors like radiation or chemicals. Changes in DNA can have various effects depending on where in the genome they occur. DNA sequence alterations can lead to either beneficial adaptations, harmful conditions, or sometimes no noticeable impact at all.

The kind of change in the DNA sequence defines the class of mutation鈥攚hether it's a simple switch of one nucleotide in a point mutation or a large alteration in a chromosomal mutation. Understanding DNA sequence changes helps scientists determine mutation causes and their impacts.
Point Mutations
Point mutations happen when a single nucleotide in the DNA sequence is altered. These represent the most basic type of mutation. There are three subtypes of point mutations: silent, missense, and nonsense.

Silent mutations do not affect the resulting protein, missense mutations change a single amino acid in the protein, and nonsense mutations cause a stop codon to appear prematurely, leading to a shorter, often nonfunctional protein.
  • Silent: No change in protein function.
  • Missense: Can alter protein function by changing one amino acid.
  • Nonsense: Typically produces a nonfunctional protein.
Despite their small scale, point mutations can significantly alter an organism's traits or health.
Frameshift Mutations
Frameshift mutations may sound straightforward, but they have a big impact. They occur when nucleotides, the building blocks of DNA, are either inserted or deleted. When this happens, it changes the reading frame of the gene by shifting it, resulting in a completely altered protein sequence downstream of the mutation site.

These kinds of mutations usually lead to proteins that are nonfunctional because every amino acid after the mutation gets jumbled due to the frame shift. Frameshift mutations illustrate the critical importance of maintaining the right nucleotide sequence. One tiny insertion or deletion can throw the entire sequence out of whack.

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Most popular questions from this chapter

Distinguish between penetrance and expressivity.

Consider the ABO blood group locus in humans, which has \(\operatorname{six}(6)\) alleles reported for it, of which three are most prominent, \(\mathrm{I}^{\mathrm{A}}, \mathrm{I}^{\mathrm{B}}\) and i. The \(\mathrm{I}^{\mathrm{A}}\) and \(\mathrm{I}^{\mathrm{B}}\) alleles are both dominant to \(\mathrm{i}\) and codominant to each other. A woman of blood group \(\mathrm{O}\) marries a man who has blood group B. There are four children in the family: a son and daughter of blood group \(\mathrm{O} ;\) a daughter who has A blood type; and a son who has \(B\) blood type. One of the children is adopted. Which child is the adopted child?

A bacterial culture is divided into two halves, \(\mathrm{A}\) and \(\mathrm{B}\), and both halves receive large but equal amounts of ultraviolet light. Culture \(B\) is then wrapped in brown paper to isolate it from any light. Culture \(\mathrm{A}\) is left unprotected from the incident visible light. After 24 hours the cultures are examined. Culture A shows much more growth than culture \(B\). Explain.

How are frameshift mutations produced?

What are multiple alleles and how do they originate?
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