Topic 4: Genetic Diversity Flashcards

(40 cards)

1
Q

define meiosis

A

A type of nuclear division that produces 4 daughter cells, each with half (haploid) the number of chromosomes of the parent cell

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2
Q

Purpose of meiosis

A

Produces genetically different daughter cells
Sexual reproduction results in genetic diversity in offspring
Survival advantage when environmental conditions change so individuals are more likely to survive

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3
Q

What are gametes?

A

They are haploid and 2 fuse together to produce an offspring with diploid number of chromosomes

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4
Q

Why are the chromosomes in homologous pairs similar?

A

One is from the male and one is from the female
They carry the same genes for the same polypeptides in the same positions (locus)

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5
Q

What are produced in meiosis?

A

4 daughter cells that aren’t identical, they are genetically different and form gametes

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6
Q

What is independent segregation?

A

It is a process of genetic variation
When homologous pairs line up on the equator , it is completely random as to which chromosomes from each pair end up together in daughter cells

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7
Q

what is the result of independent segregation?

A

New combinations of paternal and maternal chromosomes in gametes

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8
Q

When do independent segregation and crossing over occur?

A

During meiosis 1 when the homologous pairs line up

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9
Q

What is crossing over?

A

When homologous pairs line up and become twisted to form a bivalent. The bivalent causes sections of the chromatids to be swapped- so alleles were swapped.
Produces recombinant chromatids

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10
Q

define Chiasmata

A

Point where chromatids cross, break and rejoin

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11
Q

Calculation for the possible combinations of chromosomes following meiosis

A

2^n

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12
Q

2^n

A

How to calculate the possible combinations following meiosis

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13
Q

How to calculate the possible combinations after random fertilisation of 2 gametes?

A

(2^n)2

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14
Q

(2^n)2

A

How to calculate the possible combinations after random fertilisation of 2 gametes

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15
Q

Life cycle exam questions

A
  • may get given the life cycle of an unknown organism
  • meiosis will be where a diploid has divided and become haploid
    Haploid to diploid is fertilisation
    If it stays the same= mitosis
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16
Q

How many divisions are in meiosis?

A

2

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17
Q

Describe prophase 1

A

Chromosomes are visible because they have condensed

18
Q

Describe metaphase 1

A

Homologous chromosomes line up at the equator, how they line up is random

19
Q

Describe anaphase 1

A

Homologous chromosomes are pulled to opposite poles

20
Q

Telophase 1

A

Cell prepares for first cell division

21
Q

Metaphase 2

A

Individual chromosomes line up at the equator

22
Q

Anaphase 2

A

Sister chromatids are separated to opposite poles

23
Q

Telophase 2

A

Each daughter cell is haploid

24
Q

What are chromosomes mutations?

A

Changes in structure or number of chromosomes

25
What do chromosome mutations lead to?
Inherited conditions because errors are present in the gametes
26
Polyploidy
Changes in whole sets of chromosomes- all homologous chromosomes fail to seperate properly A diploid gamete is fertilised by a haploid gamete to give an organism 3 sets of chromosomes May occur in plants
27
Non-disjunction
Changes in the number of individual chromosomes- sometimes individual homologous chromosomes fail to seperate during meiosis
28
What happens as a result of non-disjunction?
The resulting gamete has one more or one fewer chromosomes than it should If a normal gamete fuses with this gamete, all resulting body cells will have the same number of chromosomes This occurs in Down’s syndrome
29
When is a mutation inherited?
They occur randomly, they are inherited if they occur in gametes but not if in somatic cells
30
what are the causes of mutations?
They can occur randomly, but substances called mutagens can increase the natural mutation rate Mutagens e.g ionising radiation, UV light, tobacco tar, mustard gas
31
Are all mutations harmful?
No They can be helpful by producing new alleles, and increasing variation in a population
32
3 types of mutation
Addition Deletion Substitution
33
What are addition and deletion known as?why?
Frameshift mutations Because they can significantly alter the resulting polypeptide chain
34
Addition
An extra nucleotide base is added
35
Deletion
A nucleotide is removed
36
Substitution
A nucleotide is replaced by one with a different base
37
Why aren’t all base substitutions bad?
The degenerate nature of the genetic code means that not all base substitutions cause a change in sequence of encoded amino acids
38
What is the effect of a mutation?
-The mutation causes a change in the sequence of bases in the dna -this leads to a change in the mRNA This leads to a change in the amino acid sequence in the polypeptide chain This causes a change in the function of a protein because it has a different tertiary structure
39
Give one example of a substitution mutation
Sickle cell anemia Caused by a substitution of one dna base which alters one amino acid and changes the structure & function of haemoglobin
40
What can mutations result in?
Differences in base sequences of alleles of a single gene may result in non-functional proteins, including non-functional enzymes