3.7.1 inheritance Flashcards

(52 cards)

1
Q

what is a gene?

A

a section of DNA that codes for a polypeptide/protein.

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2
Q

where is a gene located?

A

at a specific locus on a chromosome.

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3
Q

what is a chromosome?

A

contains many genes made of a long DNA molecule.

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4
Q

what is an allele?

A

a version of a gene, as genes can exists in different versions.

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5
Q

what is important about the location of alleles?

A

alleles of the same gene have slightly different base sequences but occupy the same locus.

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6
Q

what is a locus?

A

a section of a chromosome where a gene is located.

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7
Q

what’s the difference between a loci and locus?

A

locus is singular (a specific position of a gene on a chromosome) and loci is plural (multiple positions of genes on chromosomes).

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8
Q

how many sets of chromosomes does a diploid organism have and how many is in their gametes?

A

diploid organism has two sets of chromosomes (in homologous pairs) and therefore has two copies of each gene. they produce haploid gametes that only carry one copy of each gene.

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9
Q

what does homozygous mean?

A

individuals with identical/the same allele for a gene.

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10
Q

what does heterozygous mean?

A

individual with different alleles for a gene.

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11
Q

what is the genotype?

A

the genetic composition of an organism, all the alleles an organism possesses.

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12
Q

what is a phenotype?

A

the observable characteristics determined by genotype and the environment.

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13
Q

what is a dominant allele?

A

an allele that is always expressed in the phenotype: expressed in both homozygous and heterozygous individuals.

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14
Q

what is a recessive allele?

A

only expressed in the phenotype if no dominant allele is present: only expressed when present in a homozygous individual.

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15
Q

what is co dominance?

A

when both alleles in a heterozygous genotype are expressed: features of both alleles are expressed in the phenotype.

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16
Q

what is mendel’s first law linked to monohybrid crosses?

A

each organism has two alleles for a gene and these speerate during gametes formation (meiosis) so each gametes contains one allele. fertilisation restores the pair of alleles.

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17
Q

what is monohybrid inheritance?

A

the tracking the inheritance of one gene with two alleles.

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18
Q

what genetic diagram is used to present monohybrid crosses etc?

A

punnet square.

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19
Q

why may observed ratios in offspring differ from predictions?

A

due to random fertilisation of gametes.

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20
Q

what can you determine the genotype of an individual showing the dominant phenotype?

A

a test cross with a homozygous recessive.

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21
Q

what does a monohybrid test cross with all offspring showing the dominant phenotype tell you?

A

unknown genotype homozygous dominant.

22
Q

what does a monohybrid test cross with 50% dominant and 50% recessive tell you?

A

unknown genotype is heterozygous.

23
Q

what does a dihybrid test cross with no recessive phenotypes tell you?

A

unknown genotypes is homozygous dominant for both genes.

24
Q

what does a dihybrid test cross with at least one recessive phenotypes for one gene only tell you?

A

unknown genotype is heterozygous for one gene and homozygous dominant for the other.

25
what does a dihybrid test cross with at least one recessive phenotypes for both genes tell you?
unknown genotype is heterozygous for both genes.
26
what is linkage?
genes that are inherited together because they are on the same chromosome.
27
what are the two types of linkage?
sex linkage and autosomal linkage.
28
what is a women's sex chromosome?
two copies of the X chromosome: XX.
29
what is a man's sex chromosome?
one X chromosome and one shorter Y chromosome: XY.
30
which chromosome number is sex chromosomes?
23.
31
where are sex-linked genes located?
on the X chromosome (rarely on the Y).
32
why are males more likely to express recessive sex-linked traits?
as they only have one copy of X-linked genes.
33
why can females be carriers of sex-linked traits?
as they have two copies of X-linked genes.
34
what is a dihybrid cross?
tracks the inheritance of two genes simultaneously.
35
genetic diagrams of dihybrid crosses follow a similar structure but they include:
more genotype combinations and more phenotype combinations.
36
where does autosomal linkage occur?
in the autosomes.
37
what are autosomes?
any chromosome that is not a sex chromosome.
38
what is autosomal linkage?
two or more of the gens on the sea chromosome doe not assort independently during meiosis. these genes are linked and stay together ion the original parental combination: they will not dependently segregate during meiosis.
39
autosomal linkage: why is there sometimes unexpected phenotypes?
due to crossing over.
40
how can were work out how close together genes are on a chromosomes?
by the cross over value.
41
how do you work out the cross over value?
number of recombinant offspring/total number of offspring x 100
42
the larger the cross over value...
the more distant the genes.
43
autosomal linkage: why does crossing over sometimes not affect the genes?
as the genes are very close together on the chromosome.
44
what is epistasis?
when one gene affects the expression of another gene.
45
what is the purpose of the chi squared test?
to determine whether or not there is a significant difference between the observed and expected results in an experiment.
46
chi squared test: if difference in results are significantly different...
this suggests the presence of a factor that isn't being accounted for.
47
chi squared test: if difference in results is not significantly different...
only differences that are observed are due to chance alone.
48
what does the critical value depend on?
probability level (typically 0.05/5%) and the degrees of freedom.
49
how do you work out the degrees of freedom?
number of classes - 1
50
what criteria must be met for chi squared test?
1. large sample size. 2. data must be discrete values. 3. only raw counts, not percentages etc.
51
if chi squared value ≳ critical angle...
significant difference not due to chance, so reject null hypothesis.
52
if chi squared value < critical angle...
significant difference due to chance, so accept null hypothesis.