Topic 8 Flashcards

1
Q

In crossing over Bits of maternal and paternal chromatids join together at the

A

Chiasmata

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2
Q

What does crossing over give rise to

A

Genetic variation, making new combinations of alleles on chromosomes.

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3
Q

What are the 3 types of mutation

A
  1. Point mutation - substitution, insertion , deletion
  2. Chromosomal mutation translocation - part of chromosome breaks off and attaches on a different chromosome
  3. Chromosome mutation polysomy
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4
Q

Changing one base for another may not affect the primary structure of a protein why’s this

A

Substitution may code for the same amino acid
Due degenerate nature of the genetic code

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5
Q

What’s polygenic

A

Many genes

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6
Q

What’s autosomal gene linkage

A

Both genes found on the same homologous chromosome pair

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7
Q

When linked genes are located close to each other
on the chromosome …

A

recombination events eg crossing over) during mieosis will rarelt occur
Recombination takes place in mieosis 1

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8
Q

If genes are located further apart from each other
on a chromosome (loosely linked)

A

The number of
recombination events will be higher.

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9
Q

In unlinked genes the same 2 genes
on separate
chromosomes in different homologous pairs

A

the genes
from each
chromosome are
not linked at all so the
characteristics are
inherited independently

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10
Q

whats a dihybrid cross

A

the inheritance of 2 genes is considered at the same time

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11
Q

when will u get the ratio 9:3:3:1

A

in a dyhibrid cross if 2 heterozygous parents for both genes are crossed you get that ratio

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12
Q

however you may not get the 9:3:3:1 ratio if..

A

theres autosomal linkage or crossing over in mieosis u will get 3:1 instead (most the time)

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13
Q

crossing over DURING MIESOSIS RESULTS IN

A

new combinations of alleles in the gametes, so the predicted gametes in ur punnet square may differ

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14
Q

What is the chi squared test used for?

A

Is the difference between observed and expected data significant or due to chance?

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15
Q

When will mendellian genetics not occir

A

If the patterns. R sex linked

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16
Q

What’s a sex linked disorder

A

A genetic condition caused by a mutation in a gene located on a sex chromosome, These disorders are often associated with the X chromosome because it carries more genes than the Y

17
Q

Haemophilia is

A

A sex linked disorder caused by Mutations in the gene responsible for producing clotting factors found on the X chromosome , it affects the bloods ability to clot properly , excessive bleeding

18
Q

What’s the inheritance of haemophilia

A

Males have XY so if the X chromosome carries the faulty gene the male will have haemophilia

Females have XX the female must inherit two faulty genes one from each parent to have haemophilia, females with one faulty gene are carriers

19
Q

What’s the hardy weinberg equation?
What does each letter represent ?

A

p2 + 2pq + q2 = 1
p+q=1

p2 = frequency of homozygous dominant genotype (AA)
2pq = frequency of heterozygous genotype (Aa)
q2 = frequency of homozygous recessive genotype (aa)

20
Q

What’s hardy weinberg equation used for

A

to calculate and predict the allele frequencies in a population’s gene pool under certain conditions

21
Q

What are these conditions needed for the hardy Weinberg to be applied ? Theoretically stable

A

-no mutations ,
- The population is large
-no selection pressure

22
Q

how does mieosis give rise to genetic variation in gametes

A

crossing over, swapping of sections of choromsomes

23
Q

What is population bottleneck

A

The effect of a catastrophic event that dramatically reduces the size of a population by more than 50% and causes a severe decrease in the gene pool of a population , results in large changes in allele frequency

24
Q

When there’s very low allele freq the animals ..

A

Have little genetic diversity and Are very vulnerable to environmental change

25
Q

What’s the founder effect

A

the loss of genetic variation
that occurs when a small number of individuals leave
the main population and set up a new population,
-
LESS RESISTANCE TO ENVIRONMENTAL CHANGE

26
Q

If some of the founders are carrying lots of mutations then the main population

A

Will have reduced allele frequency

27
Q

What’s the difference between a bottleneck and founder effect

A

Founder effect is voluntary whereas bottle neck is forced

28
Q

What is stabilising

A

It reduces variation in the population , conserves phenotypes already present , selects against extreme phenotypes

29
Q

What’s directional natural selection

A

Shows a change from one phenotype to another , which is more advantageous to the environment, a selection pressure is applied

30
Q

What is disruptive selection

A

Disruptive selection favours extreme traits over the average, increasing genetic diversity and potentially leading to speciation

31
Q

What’s Genetic drift

A

Genetic drift is the random change in allele frequencies in a population due to chance, especially in small populations. It can lead to the loss of genetic variation over time.

Example: The founder effect

32
Q

Compare and contrast stabilising and disruptive selection

A

Both change frequency of alleles
Both select against some phenotypes

Disruptive select againsts the middle phenotype
Stabilising selects against extremes

33
Q

The allele for one defect in cone cells is recessive and carried on the X chromosome , why are more men than women colour blind

A

Females inherit 2 X chromosomes
So if they inherit one recessive and one dominant allele the recessive allele won’t be expressed