Mutation and Mutagens Overview

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Questions and Answers

What characteristic of the Murray breed led to its popularity among farmers?

  • Higher milk yield
  • Better flavor of meat
  • Higher productivity of calves (correct)
  • Improved disease resistance

Which beneficial trait was developed in wheat through gene manipulation?

  • Enhanced aroma
  • Amber seed color (correct)
  • Longer shelf life
  • Increased starch content

What was a significant outcome of the gamma irradiation in rice?

  • Development of disease-resistant strains
  • Increased yield variability
  • Enhanced grain size
  • Reduction in crop duration (correct)

Why cannot some japonica strains of rice be grown in India?

<p>Poor grain quality (D)</p> Signup and view all the answers

What mutation in rice could allow japonica strains to be cultivated in India?

<p>Induced mutations for indica type grains (D)</p> Signup and view all the answers

What is aneuploidy?

<p>The condition of having an abnormal number of chromosomes. (C)</p> Signup and view all the answers

Which of the following describes trisomy?

<p>A genetic condition resulting from having an extra chromosome. (A)</p> Signup and view all the answers

Which syndrome is associated with trisomy of chromosome 18?

<p>Edwards syndrome (D)</p> Signup and view all the answers

What clinical feature is common to both Patau syndrome and Edwards syndrome?

<p>Rocker-bottom feet (B)</p> Signup and view all the answers

Which of the following features is associated with Down syndrome?

<p>Single palmar crease (A)</p> Signup and view all the answers

What is not a characteristic feature of Klinefelter syndrome?

<p>Rocker-bottom feet (C)</p> Signup and view all the answers

What is a typical life expectancy for individuals with Patau syndrome?

<p>Less than one year (C)</p> Signup and view all the answers

Which genetic condition is characterized by an extra X chromosome in females?

<p>Triple X syndrome (D)</p> Signup and view all the answers

What is a mutation?

<p>An alteration in the sequence of nucleotides in DNA. (B)</p> Signup and view all the answers

Which of the following is NOT a type of mutagen?

<p>Active transport (A)</p> Signup and view all the answers

Which type of mutation is inherited and present in every cell of the body?

<p>Hereditary mutation (D)</p> Signup and view all the answers

What distinguishes somatic mutations from hereditary mutations?

<p>Hereditary mutations occur in every cell of the body. (B)</p> Signup and view all the answers

How do spontaneous mutations primarily occur?

<p>From errors during DNA replication or transcription. (B)</p> Signup and view all the answers

Which of the following is a characteristic of induced mutations?

<p>They are generally more frequent than spontaneous mutations. (A)</p> Signup and view all the answers

Which type of mutagen can be classified as biological?

<p>Bacteria (A)</p> Signup and view all the answers

What effect can somatic mutations have on cells?

<p>They can damage or make cells cancerous. (C)</p> Signup and view all the answers

What is the primary cause of induced mutations?

<p>Exposure to mutagens (D)</p> Signup and view all the answers

Which type of mutation occurs when one DNA base is replaced with another?

<p>Point mutation (A)</p> Signup and view all the answers

What result does a missense mutation produce?

<p>An altered protein with a different amino acid (A)</p> Signup and view all the answers

In what situation does a silent mutation occur?

<p>When a nucleotide change does not alter the amino acid (D)</p> Signup and view all the answers

Which type of point mutation results in a stop codon?

<p>Nonsense mutation (D)</p> Signup and view all the answers

What defines a transversion mutation?

<p>Replacement of a purine with a pyrimidine (B)</p> Signup and view all the answers

Which type of mutation does NOT affect the function of the protein?

<p>Silent mutation (A)</p> Signup and view all the answers

What is the effect of a non-functional protein caused by a mutation?

<p>It disrupts cellular metabolic processes (A)</p> Signup and view all the answers

What is the primary clinical characteristic of Turner Syndrome?

<p>Unusually short stature (D)</p> Signup and view all the answers

Which chromosomal abnormality is associated with 3.XYY syndrome?

<p>Extra Y chromosome (A)</p> Signup and view all the answers

What type of mutation in nylon bacteria allows them to consume nylon?

<p>Frameshift mutation (D)</p> Signup and view all the answers

What is one of the benefits of mutation breeding in crops?

<p>Production of traits not found in nature (B)</p> Signup and view all the answers

How does allopolyploidy occur in plant breeding?

<p>Through interspecific hybridization followed by chromosome doubling (C)</p> Signup and view all the answers

What characteristic distinguishes the non-bitter almond species from their wild counterparts?

<p>Absence of amygdalin (C)</p> Signup and view all the answers

What is a common outcome of chromosome number changes at the genome level in crops?

<p>New crop varieties with desirable traits (B)</p> Signup and view all the answers

What is a known limitation of 3.XYY syndrome in clinical terms?

<p>Most cases remain undiagnosed (C)</p> Signup and view all the answers

What is the primary consequence of a frameshift mutation?

<p>Complete alteration of the reading frame of mRNA (B)</p> Signup and view all the answers

Which type of mutation entails the removal of a portion of the chromosome?

<p>Chromosomal deletion (D)</p> Signup and view all the answers

How do chromosomal mutations generally occur?

<p>During mitosis or meiosis processes (D)</p> Signup and view all the answers

What happens during chromosomal inversion?

<p>Portions are switched or oriented in reverse (D)</p> Signup and view all the answers

Which statement accurately describes a result of chromosomal translocation?

<p>It can create chimeric chromosomes with mixed genetic material (C)</p> Signup and view all the answers

What kind of mutation is described as an insertion of extra base pairs?

<p>Frameshift mutation (C)</p> Signup and view all the answers

What would be the effect of deleting three base pairs from a DNA sequence?

<p>It removes a complete codon without changing the reading frame (B)</p> Signup and view all the answers

Which option best describes chromosomal duplication?

<p>A segment is copied, resulting in additional genetic material (D)</p> Signup and view all the answers

Flashcards

Nondisjunction

Failure of chromosomes to separate during cell division (mitosis or meiosis), resulting in abnormal chromosome numbers.

Aneuploidy

A condition where a cell or organism has an abnormal number of chromosomes.

Monosomy

A condition characterized by the absence of one chromosome (n-1).

Trisomy

A condition characterized by the presence of one extra chromosome (n+1).

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Patau Syndrome

A genetic disorder caused by trisomy 13, characterized by severe birth defects and a shortened life expectancy.

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Edwards Syndrome

A genetic disorder caused by trisomy 18, characterized by severe birth defects and a shortened life expectancy.

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Down Syndrome

A genetic disorder caused by trisomy 21, characterized by distinct physical features and varying degrees of intellectual disability.

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Klinefelter Syndrome

A genetic disorder in males caused by an extra X chromosome (47, XXY), characterized by specific physical traits.

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Mutation

A change in DNA's nucleotide sequence

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Mutagens

Substances that increase mutation rate

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Hereditary Mutation

Passed from parent to offspring

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Somatic Mutation

Mutation in body cells, not passed to offspring

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Spontaneous Mutation

Naturally occurring DNA errors, often from replication or transcription

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Induced Mutation

Mutation caused by external factors.

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Physical Mutagen

Radiation or energy causing DNA damage

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Chemical Mutagen

Chemicals that damage DNA

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Induced Mutation

A mutation caused by external factors like mutagens, not a natural error.

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Gene Mutation

Changes in the DNA's nucleotide sequence, potentially altering the protein produced.

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Point Mutation

A gene mutation where one DNA base is replaced by another, changing the codon.

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Transition (Point Mutation)

A point mutation where a purine replaces a purine or a pyrimidine replaces a pyrimidine.

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Transversion (Point Mutation)

A point mutation where a purine replaces a pyrimidine or vice versa.

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Missense Mutation

A gene mutation where a changed codon codes for a different amino acid, potentially affecting the protein's function.

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Silent Mutation

A gene mutation where a changed codon codes for the same amino acid, no effect on the protein.

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Nonsense Mutation

A gene mutation where a changed codon becomes a stop codon, resulting in an incomplete, non-functional protein.

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Wheat breeding example

Scientists used mutations in wheat to develop varieties with traits like branched ears, lodging resistance, high protein, and specific seed colors. This led to varieties like Sharbati Sonora.

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Rice mutation example

Mutations in rice, like those induced by gamma irradiation, have resulted in varieties like Reimei (high yielding) and others with improved protein content and faster growth.

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Mutation impact on animals

Selective breeding of cows led to higher productivity in their calves, showing advantageous mutations can improve animal characteristics.

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Mutation's benefit

Mutations can be helpful when they lead to qualities or characteristics that enhance fitness or traits that are desirable to humans, such as high yield, disease resistance, or specific colors.

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Mutation's harm

Mutations can be harmful if they weaken an organism's ability to survive or reproduce or if they cause negative changes, such as diseases.

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Frameshift Mutation

A mutation caused by adding or deleting nucleotides in a DNA sequence, shifting the reading frame of the mRNA, resulting in significant phenotypic changes.

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point mutation vs frameshift mutation

Point mutations change a single nucleotide, while frameshift mutations change the entire reading frame (all subsequent codons) due to insertion/deletion of nucleotides not in multiples of three. Frameshift mutations cause much greater phenotypic changes.

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Chromosomal Deletion

A mutation where part of a chromosome is lost.

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Chromosomal Duplication

A mutation where a segment of a chromosome is repeated.

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Chromosomal Inversion

A mutation where a segment of a chromosome is flipped to the opposite orientation.

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Chromosomal Translocation

A mutation where a segment of one chromosome breaks off and attaches to a different chromosome.

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Insertion Mutation

A type of frameshift mutation that adds nucleotides to the DNA sequence.

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Deletion Mutation

A type of frameshift mutation that removes nucleotides from the DNA sequence.

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Turner Syndrome

A genetic condition in females caused by missing a X chromosome, leading to specific physical characteristics.

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XYY Syndrome

A genetic condition in males caused by an extra Y chromosome, often with no visible symptoms except possible tall stature.

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Mutation Breeding

Using mutations to improve crop traits, like bigger size, color, or taste.

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Nylonase Bacteria

Bacteria that can break down nylon, potentially useful in waste treatment.

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Almond Seed Mutation

A natural mutation in almond trees that lost the bitter chemical, making them safe to eat.

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Allopolyploidy

A type of polyploidy involving combined genomes from different species.

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Murray Gray Cattle

A beef cattle breed developed through accidental mutations in traditional cattle.

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Gene mutation in almond trees

A change in the DNA sequence of almond trees that eliminates the production of amygdalin.

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Study Notes

Mutation

  • Occurs when the sequence of nucleotides in DNA changes.
  • Changes can be beneficial, harmful, or have no effect.
  • Small percentage of changes are beneficial.
  • Happens during replication or transcription when a different or incorrect nucleotide is incorporated.
  • Causes variation and new species.

Mutagens

  • Physical, chemical, or biological agents.
  • Cause direct change and damage to DNA replication.
  • Some mutagens affect replication mechanisms and chromosomal partitioning.

Types of Mutagens

  • Physical: Ionizing radiation (X-rays, gamma rays, alpha particles), ultraviolet radiation.
  • Chemical: Reactive chemicals, deaminating agents, bromine, benzene.
  • Biological: Viruses, bacteria.

Mutation: Hereditary or Somatic

  • Hereditary:
    • Inherited from a parent.
    • Present throughout a person's life.
    • Occurs in every cell of the body (germline).
    • Present in germ cells (egg or sperm).
    • Mutated gene is passed to the offspring.
  • Somatic:
    • Acquired during a person's life.
    • Occurs in specific cells.
    • Commonly caused by external factors (e.g. exposure to radioactivity, drugs, and alcohol).
    • Does not affect the egg and sperm cells.
    • Does not pass to offspring.

Spontaneous Mutation

  • Result of natural, random changes in DNA structure.
  • Undetected and unrepaired errors during DNA replication or transcription.
  • Happens due to errors in cellular enzymes such as DNA & RNA polymerases.
  • Average rate is approximately one in a million.
  • Low rate due to cellular repair mechanisms.

Induced Mutation

  • Happen with intervention of living or nonliving things (mutagens).
  • Exposure to mutagens causes induced mutations.
  • Can occur at gene, molecular or chromosomal level.

Types of Gene Mutation

  • Point Mutation: Replacement of one DNA base with another, changing the codon in RNA sequence.
    • Transition: Purine to purine (A to G or G to A) or pyrimidine to pyrimidine (C to T or T to C) change.
    • Transversion: Purine to pyrimidine or pyrimidine to purine change.
  • Missense Mutation: Mutated codon codes for a different amino acid, altering the protein.
  • Silent Mutation: Mutated codon codes for the same amino acid as the original codon, no effect on protein.
  • Nonsense Mutation: Mutated codon is a stop codon, causing premature termination of protein synthesis.

Frameshift Mutation

  • Results from addition or deletion of nucleotides in DNA sequence.
  • Shifts the reading frame of mRNA (codon reading sequence).
  • Insertion or deletion of nucleotides changes the entire frame.
  • Greater phenotypic change than point mutations.
    • Insertion: Addition of a base pair.
    • Deletion: Removal of a base pair.

Chromosomal Mutations

  • Changes in the chromosome structure affecting DNA sequence.
  • Occur during mitosis or meiosis.
  • Cell cycle processes like crossing-over and recombination may be affected.
  • Can cause abnormalities and malignancies.
    • Deletion: Portion of chromosome is deleted.
    • Duplication: Portion of chromosome is duplicated.
    • Inversion: Portions of chromosome are switched or inverted.
    • Translocation: Portion of one chromosome is transferred to another chromosome.

Nondisjunction

  • Failure of chromosomes to separate during cell division.
  • Creates daughter cells with abnormal chromosome numbers.
  • Can lead to monosomy (missing a chromosome) or trisomy (extra chromosome).

Genetic Disorders due to Nondisjunction

  • Autosomal Trisomies:
  • Patau Syndrome (Trisomy 13): Rocker-bottom feet, microphthalmia, and severe intellectual disability.
  • Edwards Syndrome (Trisomy 18): Rocker-bottom feet, low-set ears, and intellectual disability.
  • Down Syndrome (Trisomy 21): Single palmar crease, flat facial features, and intellectual disability.
  • Sex Chromosome Trisomies:
  • Klinefelter Syndrome (47, XXY): Male with extra X chromosome.
  • Triple X Syndrome (47, XXX): Female with extra X chromosome.
  • XYY Syndrome: Male with extra Y chromosome (normally not causing significant problems).

Benefits of Mutation

  • Mutation Breeding: Purposeful application in plant breeding to produce desirable traits like larger seeds/fruits, higher protein/lysine, or disease resistance.
  • Nylonase Bacteria: Bacteria mutated to eat nylon and used in wastewater treatment.
  • Almond Seeds: Mutation in wild almonds eliminated the poisonous amygdalin.

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