4.3 Genetic Diversity: Mutations & Meiosis Flashcards

1
Q

What is a substitution mutation?

A

When one base is changed for another

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2
Q

What is an insertion/addition mutation?

A

When one or more nucleotides are added into the DNA

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3
Q

What is a deletion mutation?

A

When one or more nucleotides are deleted from DNA

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4
Q

What is a point mutation?

A

When a single base pair is altered

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5
Q

What is a frameshift?

A

A knock on effect causing every amino acid after to be incorrect

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6
Q

Why are frameshifts caused?

A

Bases are read 3 at a time in a non-overlapping frame

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7
Q

What is the result of a frameshift?

A

The bonds will form in different places and the tertiary structure of the protein will be incorrect

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8
Q

What is meant by a silent mutation?

A

No change has been made to the primary structure

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9
Q

How can a mutation be silent?

A

Degenerate code means multiple codons can code for the same amino acid

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10
Q

What is a mutagen?

A

Something that increase chances of a mutation

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11
Q

What is in cells to help prevent mutations?

A

Enzymes that check the DNA after replication

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12
Q

What will happen to the cell of a healthy person if there is a mistake in DNA?

A

Apoptosis - programmed cell death
OR
There are enzymes that can fix small mistakes

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13
Q

What is apoptosis?

A

Programmed cell death

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14
Q

What is the consequence of cancer patients who don’t have the working enzymes to cause programmed cell death?

A

Cell will not undergo apoptosis
Means uncontrolled cell division and tumour growth

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15
Q

Give examples of mutagens.

A

Alcohol
Benzene
UV light
x-rays

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16
Q

What is the role of meiosis?

A

Create gametes

17
Q

What is started with in meiosis?

A

Germ line cells

18
Q

How many chromosomes do germ line cells have?

A

46

19
Q

What is a homologous pair of chromosomes?

A

Chromosomes that code for the same gene

20
Q

Where does each chromosome in an homologous pair come from?

A

One from each parent

21
Q

Are homologous chromosomes identical?

A

No they can contain different alleles (different versions of the same gene)

22
Q

How do chromosomes line up during the first division of meiosis?

A

In their homologous pairs down the centre of the cell

23
Q

Why is it important homologous pairs line up the centre of the cell during the first stage of meiosis?

A

As one from each pair needs to end up in a daughter cell

24
Q

What process can occur when homologous pairs are lined up in pairs during the first stage of meiosis?

A

Crossing over when chromosomes in homologous pairs can swap one or more alleles

25
Q

Why does crossing over increase variation?

A

Creates new combinations of alleles

26
Q

What has happened by the end of division one in meiosis?

A

DNA chromosomes have been halved from 46 to 23

27
Q

How does the amount of gametes produced in parents create increased variation?

A

Random fertilisation

28
Q

What is random segregation?

A

The allocation of gene copies is random with one of two gene copies being distributed to each gamete