Topic 3: Alleles and Inheritance (g-i)

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Define a gene

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37 Terms

1

Define a gene

A section of DNA that codes for the production of a protein

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2

Define an allele

Different form of the same gene

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3

Define phenotype

The feature that results from a genotype (the observable characteristic)

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4

Define a genotype

The allele each cell has for a certain feature

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5

Homozygous meaning

Two copies of the same allele (e.g TT or tt)

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6

Heterozygous meaning

Two different alleles (e.g Tt)

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7

Dominant meaning

The allele that is always expressed, even in a heterozygous state and is represented by a capital letter

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8

Recessive meaning

Is only expressed when there are two copies of the allele present, shown as lower case of the same letter

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9

Define a gamate

A haploid sex cell

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10

What is a zygote?

The cell formed when gamete’s fuze together in fertilisation

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11

Codominant meaning

When two alleles are expressed in the same phenotype

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12

What are all our features controlled by?

Genes which are found on chromosomes

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13

When two different alleles are in the same cell, which one is expressed?

The dominant one

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14

What is monohybrid inheritance?

  • This is the inheritance of a single characteristic.

  • It can be represented in a single diagram, called a punnet square

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15

What is a punnet square?

It shows a first generation/ set of offspring or second generation of offspring, where two individuals from the first generation are bred together

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16

Question: Pea plants can be tall or dwarf. The tall allele is dominant to the dwarf. A homozygous tall plant is crowded with a homozygous dwarf plant. Using a diagram, predict the percentage of offspring showing the different characteristics

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17

Question: Draw out a punnet square to show the offspring produced if the first generation (all tall and heterozygous- Tt) is allowed to self-fertilise to produce the second generation

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18

What are pedigree charts?

diagrams which show how genotypes and their resulting phenotypes are inherited in families

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19
<p>What is the genotype of the affected boy’s father?</p>

What is the genotype of the affected boy’s father?

Aa

<p>Aa </p>
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20

What is sex determination?

  • Sex is not controlled by a single gene, but by the presence or absence of the Y chromosome. Males have XY chromosomes, females have XX chromosomes

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21

What are the sex chromosomes of males?

Males are XY, female are XX

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22
<p>Complete the punnet square to show the sex determination in humans</p>

Complete the punnet square to show the sex determination in humans

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23

What is codominance?

If two alleles are expressed in the same phenotype, they are called codominant.

  • A letter is chosen to represent the gene and then superscript letters are used to illustrate the alleles

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24

What are the 3 alleles for the gene for blood groups?

I^A, I^B, i^O

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25

Which of the blog group alleles are dominant?

I^A and I^B

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26

Which of the alleles for blood groups is recessive?

I^O

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27
<p>Complete this table with the possible phenotypes and genotypes of the 3 alleles</p>

Complete this table with the possible phenotypes and genotypes of the 3 alleles

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28

What is meant by sex-linked gened?

Genes/ alleles that are present of the X (or Y) chromosome

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29
<p></p>

<p></p>
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30

Because males only have one copy of the X-chromosomes, how many copies of the sex-linked genes will they normally have?

One genotype: X^B Y, X^b Y

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31

If a recessive condition is caused by a gene on the X chromosome, then which sex is most likely to be affected?

Males, because females have a second recessive allele of the other X chromosome so the recessive condition is not expressed

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32

What is meant by a carrier of a disease?

How can females be carriers?

*When the condition is not shown in the phenotype but the excessive allele for the condition is on one of the X chromosomes , X^BX^b.

Females can be carrie because they have to X chromosomes so can express two different alleles. Therefore one may have the recessive condition and the other doesn’t, so they are a carrier as they have the allele for it but do not show it in their genotype

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33
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34

What is haemophilia?

A recessive, sex-linked condition carried on the X chromosome. It causes a longer than normal blood clotting time

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35
<p>A) Explain how diagram D provides evidence that haemophilia is a sex-linked disorder.</p><p>B) Explain why a female carrier of the haemophilia allele does not suffer from the disorder</p>

A) Explain how diagram D provides evidence that haemophilia is a sex-linked disorder.

B) Explain why a female carrier of the haemophilia allele does not suffer from the disorder

A) Because no female have the disorder, it is only in some males. Females are carriers

  • B) Because they have another X chromosome so the recessive condition is not expressed

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36

What is Testcross?

It is used to determine the genotype of the unknown organism.

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37

How can you use testcross to find out an unknown allele?

You cross the unknown with homozygous recessive alleles and if there is a recessive allele is in the offspring, the unknown was heterozygous

<p><span>You cross the unknown with homozygous recessive alleles and if there is a recessive allele is in the offspring, the unknown was heterozygous</span></p>
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