Meiosis and mutations Flashcards

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1
Q

Compare and contrast meiosis and mitosis

A

Comparison=
- In both, DNA is replicated at the start
- In both the daughter cells produced can be haploid

Contrast=
- In meiosis there are 2 divisions but in mitosis there’s only 1 division
- In meiosis 4 daughter cells are produced whereas in mitosis only 2 are produced
- In meiosis, crossing over and independent segregation occur whereas they don’t in mitosis
- The daughter cells are genetically identical in mitosis whereas in meiosis they are genetically different
- In meiosis homologous chromosomes separate whereas they don’t in mitosis

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2
Q

State another way genetic variation increases (not crossing over or Independent seg.)

A

Random fertilisation of gametes happens after meiosis. Each gamete is fertilised with different alleles

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3
Q

Describe what happens during Independent segregation and explain how it creates genetic variation

A

When homologus pairs line up at the equator of the cell maternal and paternal chromosomes can form different combinations

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4
Q

Describe what happens during crossing over and explain how it increases genetic variation

A
  • Homologus pairs of chromosomes associate to form a bivalent
  • Chiasmata form
  • Equal lengths of non- sister chromatids and alleles are exchanged
  • This produces new combinations of alleles in the gametes
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5
Q

What is meant by haploid?

A

A haploid cell is a cell containing one of each type of chromosome e.g. a gamete
It is represented by n

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6
Q

What is meant by diploid?

A

A diploid cell is a cell containing 2 of each type of chromosome e.g. a normal body cell
It is represented by 2n

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7
Q

What is chromosome non-disjuction?

A

A spontaneous mutation that can occur in meiosis is called chromosome non- disjunction

Homologus chromosomes (1st division) or sister chromatids (2nd division) aren’t separate forming gametes with 1 more/ 1 less chromosome.
It can lead to genetic diseases like Down syndrome

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8
Q

What are homologus chromosomes?

A

Homologus chromosomes are a pair of chromosomes which have the same genes at the same gene loci but many have different alleles

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9
Q

What is a mutation and how does it arise?

A

A gene mutation is a change in the DNA base sequence of a chromosome which leads to the formation of a new allele.

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10
Q

A mutation can lead to the production of a non- functional enzyme. Explain how (7)

A
  • mutation is a change in the DNA base sequence
  • changes the amino acid sequence of a polypeptide
  • changes the position of the hydrogen, ionic and disulphide bonds between amino acids
  • changes the tertiary structure
  • active site changes shape
  • so active site isn’t complementary to the substrate
  • no enzyme- substrate complexes form
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11
Q

Describe how a mutation can create a non- functional protein

A
  • change in the DNA base sequence
  • changes the amino acid sequences of the polypeptide
  • changes the position of the hydrogen, ionic and disulphide bonds between amino acids
  • changes the tertiary structure
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12
Q

Name some possible mutagenic agents

A
  • High energy environments- X-rays, UV radiation
  • Chemicals- benzene, asbestos
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13
Q

What is a deletion mutation?

A

when one base is removed from the DNA

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14
Q

Describe and explain the possible effect of a substitution mutation on a protein

A

Substitution mutations don’t always result in a change to the amino acid sequence. This is because the genetic code is degenerate so some amino acids are coded for by more than 1 triplet

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15
Q

What is a substitution mutation?

A

when one base is swapped for another base

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16
Q

Describe and explain the effect of the deletion mutation on a protein

A

Deletion mutations always result in a change to the amino acid sequence. This is because deletion mutations result in a frame shift so that all triplet codes and amino acids from the point of mutation change.