Inheritance Flashcards

1
Q

What is monohybrid inheritance?

A

Inheritance of a single characteristic, controlled by one gene

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2
Q

What is genetics?

A

The study of mechanisms by which an organism inherits characteristics from its parents.

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3
Q

Define gene

A

A length of DNA that codes for one polypeptide chain

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4
Q

Define allele

A

A version of a gene

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5
Q

Define locus

A

The position of a gene on a chromosome

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6
Q

Define a recessive allele

A

An allele that is only expressed in the phenotype if there is no dominant allele present

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7
Q

Define a dominant allele

A

An allele that is always expressed in the phenotype if present

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8
Q

Define codominant alleles

A

Both alleles are expressed in the phenotype of a heterozygote

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9
Q

Define phenotype

A

The characteristics of an organism resulting from both genotype and the environment

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10
Q

Define genotype

A

The alleles possessed by an organism

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11
Q

What do homozygous and heterozygous mean?

A

Homozygous means having two of the same alleles, heterozygous means having two different alleles

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12
Q

What are the sex chromosomes and what are autosomes?

A

The sex chromosomes are X and Y. Biological females are XX, males are XY. Autosomes are any of the other 22 pairs of chromosomes

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13
Q

What is a test cross and why are they done?

A

A test cross is done to identify the genotype of an individual that shows the dominant characteristic. They are crossed with a homozygous recessive individual

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14
Q

Why are males more likely to have sex linked recessive diseases?

A

Sex linked diseases have their loci on the X chromosome. Males only have one copy of the X chromosome, so if they inherit the recessive allele they will express it. Females must inherit two copies to express it.

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15
Q

What does a chi squared test show?

A

If there is a significant difference between observed and expected results

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16
Q

What are the differences between a chi squared test and a t test?

A

In chi squared data is categorical T it is continuous. In chi squared data is not normally distributed, in T it is. They both determine if there is a significant difference, but chi squared is between observed and expected, T test is between the means of two sets of data.

17
Q

What is the null hypothesis in a chi squared test?

A

That there is no significant difference between observed and expected results

18
Q

When would you reject the null hypothesis of a chi squared test?

A

When the calculated chi squared value is higher than the critical value found in the probability table for the correct degrees of freedom

19
Q

What are multiple alleles?

A

When there are more than two alleles of a gene that can code for a characteristic, such as blood types

20
Q

What is dihybrid inheritance?

A

The inheritance of two characteristics coded for by two separate genes. We assume these are on different chromosomes

21
Q

What is autosomal linkage?

A

When the genes in a dihybrid cross are both on the same chromosome, so cannot assort independently at metaphase of meiosis. This is the explanation if observed results do not match expected results in a dihybrid inheritance question

22
Q

If two genes are autosomally linked, how could you still get phenotypic combinations that are not the parental combinations?

A

By crossing over of non parental chromosomes in prophase 1 of meiosis to produce recombinants

23
Q

When do most gene (point) mutations occur in meiosis and mitosis?

A

Interphase, when the DNA is replicated

24
Q

When do most chromosome mutations occur?

A

During crossing over in prophase 1, or non-disjunction in anaphase 1 or 2 (where the chromosomes/chromatids do not separate correctly)

25
Q

Give one example of a gene (point) mutation and one example of a chromosome mutation

A

Sickle cell anaemia is a gene mutation. Down’s syndrome is a chromosome mutation

26
Q

What are silent mutations?

A

Mutations that have no effect on the phenotype

27
Q

What is a mutagen?

A

A factor that can increase the rate of mutation, such as ionising radiation. A mutagen that causes cancer is a carcinogen

28
Q

Which genes can mutate to cause uncontrolled cell division leading to cancer?

A

Either tumour suppressor genes, that normally decrease cell division. Or proto-oncogenes, which mutate to form oncogenes and increase cell division

29
Q

What is epigenetics?

A

Control of gene expression by addition or removal of tags from the DNA, without changing the DNA sequence

30
Q

What is the effect of adding methyl groups to the DNA?

A

The DNA becomes more tightly coiled around histone proteins, meaning it is transcribed less and less of the polypeptide chain is produced. The gene is silenced

31
Q

What phenotypic ratio would you see in the offspring when two heterozygotes are crossed in a simple monohybrid cross

A

0.12569444444444455

32
Q

What phenotypic ratio would you see in the offspring when two heterozygotes are crossed in a monohybrid cross with codominance

A

0.043067129629629664

33
Q

What phenotypic ratio would you see in the offspring when two heterozygotes are crossed in a dihybrid cross?