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Allele Frequency The first equation looks at the percentage of alleles in a population A + a = 1 ○ A is the percentage of dominant alleles ○ a is the percentage of recessive alleles
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There are 30 million people in Canada, so how many alleles for eye colour should there be? 60 million –two for each person If 38.9 million of those alleles are brown, what does that mean for the A and a values? A = 38.9/60 = 0.649 (64.9%) a = 21.1/60 = 0.351 (35.1%) So our equation A + a = 1 holds true (0.649 + 0.351 = 1) % dominant alleles + % recessive alleles = 100% **These are the allele frequencies
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Say in New Brunswick (population 750 000), the dominant allele frequency is 71.6% How many dominant alleles should there be? 0.716 x 1 500 000 = 1 074 000 Recessive alleles? A + a = 1 a = 1 – A = 1 – 0.716 = 0.284 (28.4%) 0.284 x 1 500 000 = 426 000
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How does this relate to population dynamics? Probability… If the dominant allele frequency is 64.9%, then we have a 64.9% chance of selecting that allele We would have a (0.649)(0.649) of selecting it twice -> (0.649)(0.649) = (0.649) 2 = 0.421 So, what is A 2 ? You may recognize it as AA -> homozygous dominant
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This means two things: 1. A random individual in Canada has a 42.1% chance of being homozygous dominant for brown eyes 2. 42.1% of individuals in Canada should be homozygous dominant This holds true for homozygous recessive a = 0.351 a 2 = (0.351) 2 = 0.123 12.3% of individuals should be homozygous recessive (blue eyes)
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What about the carriers (heterozygotes?) Aa = (0.649)(0.351) = 0.228 But, there are two ways to become heterozygous -> your father’s allele is dominant, your mother’s recessive OR you mother’s is dominant, your father’s recessive So, we multiply by 2 2Aa = 2(0.649)(0.351) = 0.456 45.6% are heterozygous
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These combine into the equation: A 2 + 2Aa + a 2 = 1 (look familiar?) This means percentage of individuals that are homozygous dominant plus heterozygous plus homozygous recessive equals 100% -> everyone! Please note that you’ll never use this equation as a whole ->you will always merely take out terms from it to do individual calculations Does it work backwards?
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Yes! If you know the percentage of people that are homozygous recessive (usually the easiest thing to identify), you can make assumptions about the allele frequency If 15.4% of people are homozygous recessive for PTC paper tasting ability, what percentage are homozygous dominant, and what percentage are carriers?
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a 2 = 0.154 a = (0.154) 0.5 (this means square root of 0.154, but I couldn’t show that on PPT ’07. Thanks Microsoft…) a = 0.392 A + a = 1 A = 1 – a = 1 – 0.392 = 0.608 With this info, the values are easy to calculate
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A 2 = (0.609) 2 = 0.370 37.0 % are homozygous dominant 2Aa = 2(0.609)(0.392) = 0.477 47.7 % are carriers All percentages add up to 100 (ok, 100.1, sig figs…)
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Example Batten disease is a rare recessive neurodegenerative disease, affecting 3 out of every 100 000 people in North America. Based on this knowledge, what percentage of people are carriers and could pass it onto their offspring?
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Answer We define the dominant, normal allele as B, and the recessive as b Since occurrence is 3 out of 100 000, b 2 =0.00003 So, frequency of recessive allele is b=√0.00003 = 0.005 The frequency of the dominant allele is B = 1-b = 1-0.005 = 0.995
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The frequency of carriers would be 2Bb=2(0.995)(0.005) = 0.0095 So, approximately 1% of the population are carriers for this disease
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Example (try on your own) It is believed that approximately 4% of Canadians of South American decent are carriers for the recessive condition sickle cell anemia. If 98% of the alleles in this population are dominant, what should the prevalence of sickle cell anemia be?
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