5.6

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

In deze les zitten 26 slides, met interactieve quizzen, tekstslides en 1 video.

Onderdelen in deze les

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

Slide 1 - Tekstslide

Let's repeat 5.5 first!

Slide 2 - Tekstslide

What is a mutation?

Slide 3 - Open vraag

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

Slide 4 - Quizvraag

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

Slide 5 - Quizvraag

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 - Quizvraag

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 - Quizvraag

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

Slide 8 - Quizvraag

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 - Tekstslide

One X of two X's

Slide 10 - Tekstslide

The y chromosome

Slide 11 - Tekstslide

Slide 12 - Tekstslide

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 - Tekstslide

Slide 15 - Tekstslide

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 - Tekstslide

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 - Tekstslide

Slide 18 - Tekstslide

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

Slide 19 - Open vraag

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

Slide 20 - Open vraag

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 - Tekstslide

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 - Tekstslide

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 - Quizvraag

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

Slide 24 - Quizvraag

Slide 25 - Video

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

Slide 26 - Tekstslide