20.1 - Gene Expression Flashcards

(10 cards)

1
Q

What is a mutation

A

Any change to the quantity or the structure of the DNA of an organism, or any change to one or more nucleotide bases or their arrangement

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2
Q

Name the three main types of base substitution consequences

A
  1. Formation of a stop codon (premature termination)
  2. Formation of a codon for a different amino acid (missense)
  3. Formation of a codon for the same amino acid (silent)
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3
Q

What is a frame shift mutation, and which two types of mutation typically cause it

A

A shift in the reading frame of the DNA, caused by the addition or deletion of a single base, which alters every subsequent triplet and changes the amino acid sequence

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4
Q

How does an inversion of bases mutation differ from a deletion or addition

A

A group of bases is separated from the sequence, reversed (put int he inverse order), and reinserted at the same position

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5
Q

What human disease is given as an example of a consequence of a base substitution mutation

A

Sickle cell anaemia, caused by a change in the protein structure that effects its shape and function

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6
Q

Name the two general categories of factors that cause mutations

A
  1. Spontaneous mutations (occurs during DNA replication)
  2. Induced mutations (caused by outside factors/mutagens)
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7
Q

Name two types of mutagenic agents (mutagens)

A
  1. High energy ionising radiation (e.g X rays, UV light)
  2. Chemicals (e.g Benzopyrene in tobacco smoke)
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8
Q

What is the main benefit of mutations

A

They produce the genetic diversity necessary for natural selection and speciation

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9
Q

What happens when a mutation occurs in a body cell (somatic cell) rather than in a gamete

A

It can disrupt normal cellular activities like cell division, which can lead to diseases such as cancer

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10
Q

Why is the formation of a different codon for the same amino acid known as a silent mutation

A

Because the genetic code is degenerate, and the resulting polypeptide is unaffected

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