Chapter 9 - Genetic Diversity, Mutation And Meiosis Flashcards

1
Q

What are gametes

A

Haploid sex cells (sperm and eggs)

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2
Q

What is meant by haploid

A

A cell with a single set of unpaired chromosomes (one of each homologous pair)

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3
Q

What is meant by a diploid

A

A cell with 2 complete sets of chromosomes (homologous pairs, one from each parent)

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4
Q

What is meant by fertilisation

A

Fusion of 2 haploid gametes to form a zygote

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5
Q

What is the definition of meiosis

A

Cell division to form gametes

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6
Q

What is the definition of mitosis

A

Cell division for growth and repair

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7
Q

How many divisions are there for meiosis

A

2 divisions

Meiosis I and II

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8
Q

How many daughter cells are produced in Mitosis

A

2

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9
Q

How can daughter cells in mitosis be described

A

Genetically identical to each other and their parent cell

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10
Q

Why are daughter cells in meiosis genetically different from each other and their parent cell

A
  • Crossing over

- Independent segregation

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11
Q

What is meant by gene mutation

A

Change to base sequence of DNA during DNA replication

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12
Q

What is meant by crossing over

A

The exchange of alleles between homologous chromosomes, resulting in a different combination of alleles

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13
Q

When does crossing over occur

A

In metaphase I

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14
Q

Draw a representation of crossing over

A

In folder

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14
Q

What is meant by independent segregation

A

Formation of random combinations of chromosomes in metaphase I, instead of homologous pairs

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15
Q

What is a substitution mutation

A

Swapping one base for another

16
Q

What is meant by a nonsense substitution mutation

A

When swapping one base for another codes for a stop codon instead of an amino acids

17
Q

What is meant by a silent substitution mutation

A

Mutation that has no effect on amino acids and therefore phenotype

18
Q

What is meant by a deletion mutation

A

One base is removed causing a frameshift

19
Q

What is meant by a frameshift

A

When all following triplets/codons change due to deletion of one base

20
Q

How can gene mutations cause a non-functional protein

A
  • Change in DNA triplet during replication
  • Change in mRNA codon
  • Change in anticodon
  • Different amino acid
  • Change in primary structure
  • Different bonding (hydrogen and ionic)
  • Change in tertiary structure of protein
  • Change shape of active site/variable region
  • Unable to form enzyme-substrate or antigen-antibody complex
22
Q

Why may a gene mutation cause no change to primary structure

A
  • DNA is degenerate
  • Each amino acid is coded for by more than one codon
  • Change to DNA base but not change amino acid coded for
  • So no Change in primary structure
  • No change to bonding
  • No change to tertiary structure
  • Can still form complex
23
Q

What is an example of a chromosome mutation

A

Chromosome non-disjunction

24
Q

What is meant by chromosomes non-disjunction

A

When chromosomes don’t separate properly in Meiosis I or II

25
Q

What is the result of chromosomes non-disjunction

A

An uneven number of chromosomes in the gametes

26
Q

What is an example of a disease caused by chromosome non-disjunction

A

Down’s syndrome