Module 4 - Genetic diversity can arise as a result of mutation or during meiosis Flashcards

1
Q

Simply explain how DNA is passed from one generation to another.

A

A haploid sperm and a haploid come together during fertilisation making a diploid cell (zygote). Fertilisation is random meaning different zygotes are produced which have different combinations of chromosomes

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2
Q

What is a homologous pair?

A

This is a pair of chromosomes - one maternal and one paternal - that are genetically identical but they can have different alleles

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3
Q

What happens before meiosis takes place?

A

DNA unravels and replicates so there are two copies of each chromosome called chromatids. DNA condenses to form double-armed chromosomes. Chromatids joined by the centromere

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4
Q

Briefly explain each part of meiosis?

A

In meiosis 1, chromosomes arrange themselves in homologous pairs. These pairs separate and half the chromosomes number. 2 diploid cells are produced. In meiosis 2, pairs of sister chromatids split producing 4 haploid cells

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5
Q

What are 2 ways in which meiosis increases genetic diversity?

A

Crossing over and independent segregation

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6
Q

What happens in crossing over?

A

This is when homologous pairs come together and a section of one chromatid per chromosome swap sections of DNA. They have the same genes but different combinations of alleles.

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7
Q

What is meant by the independent segregation of chromosomes

A

When a chromosome from each homologous pair moves into each daughter cell, the process is completely random so the 4 haploid cells produced have completely different combinations of alleles which then leads to complete genetic variation

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8
Q

3 differences between mitosis and meiosi

A
  • Mitosis produces 2 daughter cells whereas meiosis produces 4
  • mitosis produces diploid cells whereas meiosis produces haploid cells
  • mitosis produces genetically identical cells whereas meiosis produces genetically different cells.
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9
Q

Haploid and diploid difference

A

Haploid 2n
Diploid n

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10
Q

What is a chromosome mutation? What can it lead to?

A

An error created during meiosis. Leads to inherited conditions because errors are present in gametes.

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11
Q

What is meant by non-disjunction?

A

This is the failure of chromosomes to separate properly

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12
Q

What are 2 types of mutations?

A

Deletion and Substitution

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13
Q

What is meant by deletion?

A

This is when one base is remove from a sequence which causes a frameshift of base triplets therefore the DNA sequence after the deletion will create a change in the polypeptide

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14
Q

What is meant by substitiution?

A

This is when one base is substituted for another base

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15
Q

Why might substitution mutations not impact the protein being made?

A

Some base triplets are degenerate which means that multiple DNA triplets code for the same amino acid therefore the mutation may code for the same amino acid.

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16
Q

What is a mutagenic agent?

A

This is something that increases the rate of mutation

17
Q

What are some examples of a mutagenic agent?

A

Ultraviolet radiation, ionising radiation and some chemicals can increase the rate of mutations which impacts protein formation