5.6

It runs in the family
5.6 The difference of being a boy or girl
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Slide 1: Slide
BiologieMiddelbare schoolhavo, vwoLeerjaar 3

This lesson contains 26 slides, with interactive quizzes, text slides and 1 video.

Items in this lesson

It runs in the family
5.6 The difference of being a boy or girl

Slide 1 - Slide

Let's repeat 5.5 first!

Slide 2 - Slide

What is a mutation?

Slide 3 - Open question

True or false:
A mutation usually doesn't have an effect in the phenotype
A
True
B
False

Slide 4 - Quiz

Are mutations always negative?
A
yes
B
no
C
no idea

Slide 5 - Quiz

In what type of cells do mutations have the greatest effect on our body?
A
red blood cell
B
egg cell
C
brain cell
D
white blood cell

Slide 6 - Quiz

A man has a mutation in his body cells that causes him to have superpowers. The gene is located only on one chromosome. What is the chance that his child will have his superpowers?
A
0%
B
25%
C
50%
D
100%

Slide 7 - Quiz

True or false:
cancer can be the result of a mutation
A
True
B
False

Slide 8 - Quiz

Goals
- Why do certain inherited diseases occur more often in boys than in girls?
- Given a certain combination of parents, how can you determine the genotypes and phenotypes of sex-linked inherited characteristics in the off spring?



Slide 9 - Slide

One X of two X's

Slide 10 - Slide

The y chromosome

Slide 11 - Slide

Slide 12 - Slide

Could you see all the numbers?
Yes
Nothing
Not all of them

Slide 13 - Poll

Do you remember?
A recessive allele has to occur twice (on each chromosome) in order to be expressed. If a recessive allele is accompanied by a dominant allele on the other chromosome, the dominant allele will be expressed instead.

Slide 14 - Slide

Slide 15 - Slide

Take colour-blindness for example. This characteristic is caused by a recessive allele on the X chromosome. A boy with this allele on his X chromosome is colour-blind. A girl needs not one, but two recessive alleles to be colour-blind.



Slide 16 - Slide

Color-blindness
XB stands for normal vision
Xb stands for colour-blindness
The mother is a carrier for colour-blindness: XB Xb
The father is not colour-blind: XB Y

Slide 17 - Slide

Slide 18 - Slide

What do you think the genotypes of the parents should be in order to have a daughter who is colour-blind?

Slide 19 - Open question

Can boys be carriers too for color blindness? Explain why/why not?

Slide 20 - Open question

It runs in the family
The last royal Russian couple (who lived at the beginning of the 20th century) were Tsar Nicholas Romanov and Tsarina Alexandra, who was a carrier for haemophilia. Although their four daughters, Olga, Tatiana, Maria and Anastasia, did not have haemophilia (some of them may have been carriers), the only son and heir to the throne, little prince Alexei unfortunately did.

Slide 21 - Slide

Question
What are the chances that one of Alexei’s sisters was a carrier of haemophilia? Would Tsar Nicholas and Tsarina Alexandra always produce sons with haemophilia? Why or why not?

Slide 22 - Slide

What are the chances that one of Alexei’s sisters was a carrier of haemophilia?
A
0%
B
25%
C
50%
D
100%

Slide 23 - Quiz

Would Tsar Nicholas and Tsarina Alexandra always produce sons with haemophilia?
A
Yes
B
No

Slide 24 - Quiz

Slide 25 - Video

Get to work with the bikini bottom genetics. Done? Make 5.6 

Slide 26 - Slide