19 - Genetics Of Living Systems Flashcards

(31 cards)

1
Q

Define a mutation

A

A change in the sequences of bases in DNA

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2
Q

What causes the change in sequence in a mutation?

A

Deletion, substitution or insertion

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3
Q

What is it called if only one nucleotide is affected by a mutation?

A

A point mutation

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4
Q

The substitution of a single nucleotide causes what to occur?

A

Changes the codon, so a new a.a. is coded, changing the 1Y of the protein

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5
Q

How can substitution not actually affect the protein?

A

Due to degenerate nature of code, the new codon may still code for the same a.a.

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6
Q

What does the insertion or deletion of a nucleotide(s) cause!

A

Frameshift mutation

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7
Q

What is the reading frame of a sequence of bases?

A

The triplet code that transcribes consecutively in non-overlapping groups of 3

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8
Q

How many bases equals an amino acid?

A

3 bases

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9
Q

What does the addition or deletion of nucleoside do!

A

Shifts the reading frame of the sequence of bases, changing every successive codon from the point of mutation

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10
Q

In what circumstance would the reading frame not be changed in addition or deletion?

A

If the multiples of 3 correspond to fill codons

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11
Q

What does it mean if a mutation has no effect?

A

The phenotype isn’t changed and normal functioning proteins are synthesised

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12
Q

What does it mean if a mutation is damaging?

A

The phenotype of an organism is affected in a negative way which can interfere with essential processes

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13
Q

What does it mean if a mutation is beneficial?

A

The mutation provides a useful characteristic to improve survival

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14
Q

What is a mutagen?

A

A chemical, physical, or biological agent which causes mutations

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15
Q

How are mutations described?

A

As spontaneous

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16
Q

What does the mutation of an absence of a base lead to?

A

The insertion of an incorrect base through complementary base pairing during DNA replication

17
Q

What are free radicals?

A

Oxidising agents

18
Q

What can free radicals do to nucleotides?

A

Affect their structure and disrupt base pairing

19
Q

Why are antioxidants known as anti carcinogenic?

A

Due to their ability to negate the effects of free radicals

20
Q

What are silent mutations?

A

They have no effect on the phenotype of an organism

21
Q

What are nonsense mutations?

A

These reused in a codon becoming a STOP codon instead of an amino acod

22
Q

What are missense mutations?

A

This results in the incorrect amino acid in the 1Y

23
Q

Beneficial Mutations

Where is the ability to digest lactose most commonly found?

A

In European populations who are more likely to farm cattle

24
Q

Beneficial Mutations

The majority of mammals become lactose intolerant after they what?

A

Cease to suckle

25
Where do gene mutations occur?
In single genes or sections of DNA
26
Where do chromosome mutations affect?
The whole chromosome or number of chromosomes in a cell
27
What normally causes chromosome mutations?
Caused by mutagens normally in meiosis
28
Chromosome mutations How does deletion change chromosome structure?
Section of chromosomes breaks off and is lost
29
Chromosome mutations How does duplication affect?
Sections get duplicated on a chromosome
30
Chromosome mutations How does translocation affect chromosome structure?
A section of one chromosome breaks off and joins another non-homologous chromosome
31
Chromosome mutations How does inversion affect the chromosome structure?
A section breaks off, is reversed, and joins back onto the chromosome