topic 8.1 & 8.2 Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

what is genetic variation

A
  • new versions and combination of genes fro the survival and evolution of new species
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what re 3 ways that genetic variation occurs

A
  • meiosis
  • mutations
  • random fertilisation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

why are human traits difficult to control

A
  • humans are polygenic hence lots of genes are responsible for a trait - nature
  • due to the uterus environment where it grows - nurture
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

how does meiosis result in genetic variation

A
  • production of haploid gametes
  • when chromosomes align in pairs in metaphase 1 they can arrange with maternal and paternal on either side
  • independent assortment
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

how does crossing over act as a source of genetic variation

A
  • during prophase 1, an enzyme cuts and sticks parts of maternal and paternal chromosomes between the homologous pairs at the chiasmata
  • lots of new allele combination are created
  • results in genetic variation
  • potential source of mutation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how do mutations act as a source of genetic variation

A
  • there is a permanent change in the DNA
  • single codon changes which affects the proteins produced
  • gametes are formed (meiosis)
  • somatic cell division (mitosis)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

3 examples of genetic disorders

A
  • down syndrome
  • cystic fibrosis
  • sickle cell anaemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

3 types of mutation

A
  • point
  • chromosomal
  • chromosome
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

point mutation

A
  • change in one or a small number of nucleotides
  • includes deletion, insertion & substitution
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

chromosomal mutation

A
  • a change to the position of genes within a chromosome
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

chromosome mutation

A
  • when an entire chromosome is lost or gained
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

random fertilisation - egg

A
  • every month a selection of ova mature
  • random selection of 1 egg to be released
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

random fertilisation - sperm

A
  • ejaculation : 2-5cm^3 of sperm released
  • 20-150 million sperm per cm^3
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

genotype

A

all of the genetic information in an organism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

phenotype

A

the physical and biochemical characteristics of an organism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

homozygote

A

an individual where both the alleles coding for a particular characteristic are identical

17
Q

heterozygote

A

an individual where both the alleles coding for a particular characteristic are different

18
Q

dominance

A

when a phenotype shows dominance it is expressed whether the individual is homozygous for the characteristic or not

19
Q

recessive

A

when a phenotype is recessive it is only expressed when both alleles code for a recessive feature

20
Q

codminance

A

two versions of the same gene are expressed separately to yield different traits in an individual

21
Q

multiple alleles

A

cases where the population has more than two alleles of the same gene

22
Q

inheritance of two non-interacting genes

A
  • they will be inherited independently of each other
  • the expected ratios of offspring with each characteristic will be the same as if the genes were considered seperately
23
Q

what is the ratio is dihybrid inheritance

A

9 : 3 : 3 : 1

24
Q

9 : 3 : 3 : 1 ratio explained

A
  1. the four different gametes arise because the chromosomes arrange randomly during meiosis
    • AB ab Ab aB -> gametes
  2. the ratio is all combinations of two 3 : 1 ratios
    - (3P + 1p) (3T + 1t) = (PT + 3Pt + 3pT + pt
  3. probability of purple and tall is given by the probability of purple times probability of tall
    • 3/4 x 3/4 = 9/16
25
Q

what are autosomes

A

any chromosome that is not involved in inheritance of sex

26
Q

autosomal linkage

A
  • genes located on the same chromosome may be inherited together - autosomal linkage
27
Q

result of autosomal linkage

A
  • most gametes have the combination of alleles found in parents’ chromosomes
  • only when DNA is swapped between chromosomes in crossing over can recombinant gametes be produced
28
Q

how can meiosis bring about autosomal linkage

A
  • crossing over
  • new combinations of alleles can be produced in gametes as a result of crossing over
29
Q

linked genes

A
  • do not show independent assortment as the combinations of alleles passed down from parents will tend to stay together
30
Q

demonstrating linkage - Drosphila

A
  • flies normally have grey bodies & long wings
  • recessive alleles exist for black bodies & vestigial wings
  • G, L, g, l
31
Q

offspring produced by crossing

A

GL = 965
Gl = 206
gL = 185
gl= 944

not a 1: 1: 1: 1 ratio that was expected from this cross

32
Q

genotype
possible gametes
offspring
phenotype
probability

A
  • GL, gl, gl gl
  • GL gl gl
  • GL gl gl gl
  • grey long, black vestigial
  • 1/2, 1/2
33
Q

what does linkage do to the number of parental type offspring

A
  • the number of parental type offspring is higher than recombinants
34
Q

sex linkage

A
  • occurs when genes have their locus on the X chromosome
35
Q

e.g. of sex linkage

A

haemophilia

36
Q

what is haemophilia

A
  • a disorder caused by the recessive allele of a gene on the X chromosome
  • it is more common in males because the Y chromosome does not carry a copy of the gene
  • the allele on the one X chromosome will be expressed
37
Q

features of sex linkage in humans

A
  • males always have XY and females XX
  • males are more likely to be affected because they can’t be heterozygous
  • heterozygous females are carriers
38
Q
A