BSCI222 Extensions to Inheritance

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38 Terms

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how to tell if a trait is Mendelian or not?

use Chi square analysis

= Sum of (O - E)^2/E

- do for all possible genotypes and sum them up

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complete dominance

heterozygotes have same phenotype as homozygotes (Mendelian)

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wildtype allele

most common allele variant in a population

- denoted as __+

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non-wildtype allele

least common allele variant in a population

- denoted as __-

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Incomplete dominance

heterozygotes display intermediate phenotype

1:2:1 phenotypic ratio

- example: mix of colors

<p>heterozygotes display intermediate phenotype</p><p>1:2:1 phenotypic ratio</p><p>- example: mix of colors</p>
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Codominance

heterozygotes show both phenotypes at once

- example: colors or blood type

<p>heterozygotes show both phenotypes at once</p><p>- example: colors or blood type</p>
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Pleiotropy

single gene determines multiple distinct and sometimes unrelated phenotypes; ONE GENE CODES FOR MANY THINGS

- example: albinism causes loss of pigmentation in many areas

<p>single gene determines multiple distinct and sometimes unrelated phenotypes; ONE GENE CODES FOR MANY THINGS</p><p>- example: albinism causes loss of pigmentation in many areas</p>
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can pleiotropy alleles be recessive or dominant?

they can be both regarding specific genes

Example: achondroplasia, allele is dominant; if two dominant alleles are inherited, makes it lethal (so recessive for lethality)

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Lethal allele

allele that causes death early in development

- anyone in progeny with lethal allele are not observed in offspring ratios

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More than two alleles

multiple variants of alleles are present in a population, each individual still only has 2, but there is greater selection

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penetrance

the percentage if individuals having a particular genotype that express the expected phenotype

- observed/expected

<p>the percentage if individuals having a particular genotype that express the expected phenotype</p><p>- observed/expected</p>
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expressivity

degree to which a phenotype is expressed from the same genotype (not based on heterozygous genotype like in incomplete dominance)

<p>degree to which a phenotype is expressed from the same genotype (not based on heterozygous genotype like in incomplete dominance)</p>
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sex-influence traits

for same genotype, phenotype is expressed more or more fully in one sex

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sex-limited traits

phenotype is expressed only in one sex, occurs despite being autosomal trait

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phenotype expression affected by environment

phenotype expression or prevalence is affected by an environmental condition

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conditional phenotype

plays into environmental expression: allele/genotype determines susceptibility to developing a particular phenotype

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relationship/difference between gene expression and penetrance

penetrance is how many express it, expression is how much it is expressed

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ways that alleles for more than one gene affect phenotypes

1. heterogenetic traits

2. polygenetic traits

3. novel phenotypes

4. epistasis

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heterogenetic traits

traits for which non-wildtype phenotypes can be caused by many genes due to dominance variation at different loci

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complementation test

used to determine the location of recessive, non-wildtype alleles occur at the same locus or are coded by 2 separate alleles at 2 different loci

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what are the two hypotheses for complementation test?

1. alleles a and b both encode for the gene and occur on separate loci

2. alleles a and b both encode the gene but occur on the same loci

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how to test hypothesis 1 of complementation test?

cross two individuals who have two recessive, non-wild type alleles and two wild type alleles at different loci and observe gamete outcomes

example: ab+/ab+ X a+b/a+b = a+ab+b gametes

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how to tell if hypothesis 1 of complementation test is correct?

wildtype phenotype is produced, then alleles are complementary (occur at different loci)

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how to test hypothesis 2 of complementation test?

cross two individuals who both have two different alleles for the same gene (more than 2 alleles) which occurs on the same loci

example: a/a X b/b = ab gametes

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how to tell if hypothesis 2 of complementation test is correct?

nonwild type phenotype is produced

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polygenetic traits

traits which phenotypes are encoded by genes at many locations, results in wide distribution of phenotypes

example- skin color, height

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novel phenotypes

two genes act independently of each other and when fusion of gametes occurs it results in novel (new) phenotypes

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epistasis

gene interaction where one gene masks or suppresses another gene at a different locus

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epistatic gene

does the affecting in epistasis

- in labs = ee locus affects coat color

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hypostatic gene

gets affected by the epistatic gene

- in labs = loci which does fur color can be controlled by another gene at a different locus

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dominant epistasis ratio and number of phenotypes

12:3:1 and 3 phenotypes

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Recessive epistasis ratio and number of phenotypes

9:3:4 and 3 phenotypes

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recessive epistasis

homozygous recessive genotype at the epistatic gene will cause masking of hypostatic gene

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dominant epistasis

dominant genotype at the epistatic gene will cause masking of hypostatic gene

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duplicate dominant epistasis

dominant allele at either of the two genes will hide the other gene

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duplicate recessive epistasis

homozygous recessive genotype at either gene will cause masking of the other gene

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duplicate dominant epistasis ratio and number of phenotypes

15:1 and 2

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duplicate recessive epistasis ratio and number of phenotypes

9:7 and 2