Gene Mutations Flashcards

1
Q

What is a mutation?

A

Any change to the quantity or structure of the DNA of an organism

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2
Q

What is a gene mutation?

A

Any change to one or more nucleotide bases, or any rearrangement of the bases in the DNA of an organism

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3
Q

Gene mutations might arise during

A

Replication of DNA

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4
Q

What is substitution of bases (substitution)?

A

Type of gene mutation in which a nucleotide in a section of a DNA molecule is replaced by another nucleotide that has a different base

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5
Q

What are 3 possible consequences of base substitution?

A

1- formation of 1 of 3 stop codons marks end of polypeptide chain = production of polypeptide coded for by the section of DNA would be stopped prematurely = final protein would almost certainly be significantly different and the protein could not perform its final function

2- formation of codon for a different amino acid = structure of polypeptide produced would differ in a single amino acid- the protein of which this polypeptide is a part may differ in shape and not function properly e.g. if enzyme, its active site may no longer fit the substrate and so enzyme-substrate complex cannot be formed and enzyme won’t catalyse reaction

3- the formation of a different codon but codes for the same amino acid as before due to genetic code’s degenerative nature = mutation has no effect on polypeptide produced = mutation has no effect

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6
Q

What is deletion of bases (deletion)?

A

Loss of a nucleotide base from a DNA sequence

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7
Q

Why is the effect of deletion on the phenotype often enormous?

A
  • one deleted base causes frame shift
  • because the reading frame that contains each three letters of the code has been shifted to the left by one letter
  • gene is now read in the wrong three-base groups and so the coded information is altered
  • mist triplets will then be different, as will the amino acids they code for
  • the polypeptides will be different and lead to the production of a non-functional protein that could considerably alter the phenotype
  • so ultimately, one deleted base at the very start of the sequence for example could alter every other triplet from that point in the sequence
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8
Q

What are other types of gene mutation?

A
  • addition of bases
  • duplication of bases
  • inversion of bases
  • translocation of bases
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9
Q

What is addition of bases?

A

Extra base becomes inserted into the sequence

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10
Q

What is usually the effect of base addition?

A
  • Usually similar effect as base deletion in that there is usually a frame shift and the whole sequence of triplets from the point of mutation becomes altered
  • if three extra bases are added, or any multiple of three bases, there will not be a frame shift- the resulting polypeptide will be different from the one produced from a non-mutant gene, but not to the same extent as if there were a frame shift
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11
Q

What is duplication of bases?

A

One or more bases are repeated

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12
Q

What is the effect of duplication of bases?

A

Frame shift to the right

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13
Q

What is inversion of bases?

A

A group of bases become separated from the DNA sequence and rejoin at the same position but in the inverse order (back to front) = effects amino acid sequence that results

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14
Q

What is translocation of bases?

A

A group of bases become separated from the DNA sequence on one chromosome and become inserted into the DNA sequence of a different chromosome

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15
Q

What is often the effect of translocation of bases?

A

Significant effects on gene expression leading to an abnormal phenotype- these effects include the development of certain forms of cancer and also reduced fertility

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16
Q

Gene mutations can arise spontaneously during DNA replication- spontaneous mutations are

A

Permanent changes in DNA that occur without any external influence

17
Q

Despite gene mutations being random occurrences, mutations occur with predictable frequency- the natural mutation rate varies from species to species, but is typically around

A

One or two mutations per 100,000 genes per generation

18
Q

The basic mutation rate can be increased by

A

Mutagenic agents

19
Q

Give some examples of mutagenic agents

A

1- high energy ionising radiation such as x-rays and UV light (these forms of radiation can disrupt the structure of DNA

2- chemicals such as Benzopyrene, a constituent of tobacco smoke, is a powerful mutagenic agent that inactivates a tumour-suppressor gene TP53 leading to cancer

20
Q

Mutations have both cost and benefits- what are some benefits?

A

provide genetic diversity necessary for natural selection and speciation

21
Q

Mutations have both cost and benefits- what are some costs?

A
  • almost always harmful and produce an organism that is less suited to its environment
  • mutations that occur in body cells rather than in gametes leads to the disruption of normal cellular activities such as cell division, for example, cancer
22
Q

A translocation mutation is, in effect, a combination of two other different types of gene mutation- deduce which two types of mutation these are

A

Deletion and addition as the bases have been deleted from one chromosome and added to a different one

23
Q

Explain why the effects of a single additional base in a sequence of DNA may have a considerable effect on the polypeptide produced

A
  • will cause a frame shift causing codons in a sequence to be read differently as each has been shifted to the right by one base
  • if the additional base is inserted early in the sequence, most codons will be changed and so will the amino acids they code for
  • resultant polypeptide will be very different from normal
24
Q

Explain why the effects of a single additional base in a sequence of DNA may have little effect on the polypeptide produced

A
  • if the additional base is inserted at the end of the sequence, few, if any codons, will be changed
  • few, if any, amino acids they code for will differ
  • resultant polypeptide will be normal or near normal
25
Q

A mutation causes three bases in the DNA of a gene to become duplicated. Explain how the effects of this mutation might differ if the duplicated bases are consecutive rather than in three separate locations on the DNA molecule

A
  • where the duplicated bases are consecutive, the frame shift is three bases long so the subsequent codons are not affected
  • polypeptide will have an additional amino acid but otherwise unchanged
  • if the bases are separate, the frame shift will initially be one base long, becoming two bases long after the second duplicate base is added
  • codons after both duplications will be changed and the polypeptide will have many different amino acids not necessarily all (degenerate code)
  • after the third duplicate base, the codons will be unchanged
26
Q

Suggest 2 reasons why the addition of a single base into a DNA sequence may not alter the amino acid sequence in the resultant polypeptide

A
  • some codons will be changed to ones that code for same amino acid (degenerate code)
  • frame shift might not alter some codons because the replacement bases are the same as the originals