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Biblioteka

POPULATION GENETICS, SELECTION, AND EVOLUTION

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Posljednje ažuriranje 2 months ago
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Pitanje 1
1.

Total number of alleles in population =

Pitanje 2
2.

Probability of dominant allele (decimal) =

Pitanje 3
3.

Probability of recessive allele (decimal) =

Pitanje 4
4.

Calculating Allele Frequencies - p + q = 1

Stavka koja se može prevućiarrow_right_altOdgovarajuća stavka

q =

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.25

p is the

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.75

p + q = 1

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1

q is the

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dominant allele

p + q =

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recessive allele

p =

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is used to figure out allele frequencies

Pitanje 5
5.

Calculating Genotypes Frequencies - p2 + 2pq + q2 = 1

Stavka koja se može prevućiarrow_right_altOdgovarajuća stavka

p2 = (percent)

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.0625

BB = (decimal)

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.563

p2 + 2pq + q2 = 1 is used to figure out...

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.376

q2 = (percent)

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6.25%

Bb = (decimal)

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37.6%

2pq = (percent)

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56.3%

bb = (decimal)

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genotype frequencies

Pitanje 6
6.

Hardy Weinberg Equilibrium - link - more help (Bozeman)

Pitanje 7
7.
Pitanje 8
8.
Pitanje 9
9.

Sickle Cell Disease - starting population = total = 60 people; 15 homozygous dominant (HbA/HbA), 30 heterozygous (HbA/HbS), 15 homozygous recessive (HbS/HbS). Check the data table below to make sure you understand the data.

Pitanje 10
10.

Go to https://www.biologysimulations.com/population-genetics. Set everything to what you see here... The red alleles is the A frequency and the Blue allele is the S frequency on the chart.

Simulation 1 - In this sim the allele frequencies are both .5, the starting population is as the data table above sets up and their is no selective advantage for any genotype. Run the sim 5x for 5 generations (the smallest possible), recording the final allele frequencies for each sim on your own separate data table. Take the mean of the 5 allele frequencies that you recorded and record in the 1.2 data table here

Pitanje 11
11.

For simulation 1, is evolution occuring? How do you know? If so, which of the five fingers is acting to cause evolutionary change? What would you have to do to bring this population into Hardy Weinberg equilibrium?

Pitanje 12
12.

Simulation 2 - 100% negative selection against sickle cell anemia - HbS/HbS - set up as you see below - then run the sim 5x for 5 generations (the smallest possible), recording the final allele frequencies for each sim on your own separate data table. Take the mean of the 5 allele frequencies that you recorded and record in the 2.1 data table here

Pitanje 13
13.

Sim 2 Generation 2 - Repeat the same 100% negative selection continuing from where you left off in table 2.1 - So type your 2.1 genotype frequencies into the sim and run the sim 5x for 5 generations (the smallest possible), recording the final allele frequencies for each sim on your own separate data table. Take the mean of the 5 allele frequencies that you recorded and record in the 2.2 data table here

Pitanje 14
14.

For simulation 2 (both parts), is evolution occuring? How do you know? If so, which of the five fingers is acting to cause evolutionary change? What would you have to do to bring this population into Hardy Weinberg equilibrium?

Pitanje 15
15.

Heterozygote Advantage - Sim 3 will model the heterozygote advantage - set the sim as you see below - run the sim 5x for 5 generations (the smallest possible), recording the final allele frequencies for each sim on your own separate data table. Take the mean of the 5 allele frequencies that you recorded and record in the 3.1 data table here

Pitanje 16
16.

Sim 3 Generation 2 - Repeat the same 100% negative selection ALONG WITH the 50% selections AGAINST AA (heterozygote advantage) continuing from where you left off in table 3.1 - So type your 3.1 genotype frequencies into the sim and run the sim 5x for 5 generations (the smallest possible), recording the final allele frequencies for each sim on your own separate data table. Take the mean of the 5 allele frequencies that you recorded and record in the 3.2 data table here

Pitanje 17
17.

For simulation 3 (both parts), is evolution occuring? How do you know? If so, which of the five fingers is acting to cause evolutionary change? What would you have to do to bring this population into Hardy Weinberg equilibrium?

Pitanje 18
18.

What simulation might represent a population of people of African descent living in the Minnesota OR a population of Africans living in the DRY highlands of Africa? Explain!

Pitanje 19
19.

What simulation might represent a population of people living in the moist lowlands of East Africa? Explain!

Question 20
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Question 21
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Question 22
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Question 23
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Question 24
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Question 25
06:24
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Question 26
07:16
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Question 27
07:34
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Question 28
09:01
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Question 29
10:48
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Pitanje 30
30.

Explain how CRISPR is being used to cure sickle cell anemia

Pitanje 20
20.

What is different about this new treatment for SCD?

Pitanje 21
21.

The discovery of CRISPR - Cas9 sequences in bacterial DNA represented the discovery of a type of bacterial ....

Pitanje 22
22.

If a bacterium survives a viral infection, it will ...

Pitanje 23
23.

If a bacterium has a CRISPR sequence that matches a new infection, it will

Pitanje 24
24.

What was different about this DNA cutting system?

Pitanje 25
25.

Not only can this system cut DNA specifically, but ....

Pitanje 26
26.

BCL11A is a gene that makes a transcription factor that ....

Pitanje 27
27.

What is done to the BCL11A gene?

Pitanje 28
28.

What were the results of this procedure?

Pitanje 29
29.

What is different about CRISPR compared to earlier gene therapy procedures?