Gene interaction Flashcards

1
Q

What is the difference between the molecular basis of dominance? (ie. Is there dominance or recessive terms)

A

The dominance of one allele over another is determined by the protein product of that allele: phenotypic
basis
- Overall phenotype is the consequence of the activities of the protein products of the alleles of the gene

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2
Q

Define and understand halpoinsufficient gene?

A

One wild type dose produces insufficient amounts of protein product for a normal phenotype.

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3
Q

What are wild type alleles? Are they usually recessive or dominant?

A
  • mutant allele dominant to wild type
  • When the mutant allele produces less of an enzyme, and on copy, of a wild-type allele is unable to produce normal function (haploinsufficient)
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4
Q

What are the two types of functional effects of mutant alleles?

A
  • Loss of function: significant decrease or complete loss of functional gene product
  • Gain of function: gene product acquires a new function or expresses increased wild-type activity
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5
Q

incomplete dominance genotypic and phenotypic

A

heterozygous individuals display intermediate phenotypes between either homozygous type, usually being more similar to one of the homozygous types
- Neither trait is dominant, each dose of wild-type adds more pigment
- Red flower + white flower = pink flower
- 1:2:1

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6
Q

codominance genotypic and phenotypic

A

leads to heterozygotes with a different phenotype than that of either homozygote
- Detectable expression of both alleles in heterozygotes, may exhibit either or both
- ABO blood type
- 1:2:1

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7
Q

In mice, the yellow allele is lethal when homozygous and dominant to the agouti allele in heterozygotes. In a cross between two yellow mice, what will the phenotype of the offspring be?

A

All yellow mice are heterozygous because it is a recessive embryonic lethal, A^yA^y will be lethal

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8
Q

Dominant lethal alleles are, in most cases, eliminated from populations. In which case can they persist in a population? Give an example

A

If they have a late stage of onset
- Ex: Huntington’s disease - autosomal dominant

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9
Q

Imagine that you are a Labrador breeder and you have a pair of dogs with known genotype for coat color: your male has the genotype (bbEe) and your female (BBee).
a. What are the colors of your two dogs?
b. Your friend wants to buy a chocolate Labrador and you offer him to sell one of the puppies from a cross between your dogs. Will your dogs be able to produce a
chocolate puppy? What is the name of this type of gene interaction?

A

a. Male is chocolate, Female is yellow
b. Recessive epistasis (1:1 black and yellow)

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10
Q

What is pleiotropy? Give an example.

A

It is the alteration of multiple distinct traits by a mutation in a single gene.
- Drosophila, juvenile hormone influences numerous attributes of development and reproduction
such as body size, development, sexual maturity, and others
- Sick cell disease, many red blood cells of people with this take on a sickle shape and cause
numerous physical problems and complications -> range of phenotypic consequences
- Deafness in blue eyed white cats
- Apaloosa coat color and night-blindness

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11
Q

Complementary Analysis: why is it important and what can it distinguish?

A

Cis-trans test determines whether two mutations associated with a specific phenotype represent two different forms of the same gene or are variations of two different genes

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12
Q

Define and understand haplosufficient

A

Both +/+ and +/m produce sufficient
amounts of protein product for a normal phenotype.

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13
Q

complete penetrance

A

If a given genotype always produces the same phenotype. The genes for a trait are expressed in all the population who have the gene

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14
Q

Penetrance

A

the percentage of individuals that show
at least some degree of expression of the mutant genotype in a population
- partial penetrance

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15
Q

Expressivity

A

The range (‘degree’) of expression of the mutant phenotype
- Can be the result of genetic background differences and/or
environmental effects

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16
Q

incomplete Penetrance

A

the genetic trait is expressed in only part of the population

17
Q

variable expressivity

A

individuals who carry the alleles for a trait show a phenotype but to a varying degree of severity or form of expression: the variation in phenotypic expression

18
Q

Epistasis

A

When an unrelated gene affects the phenotypic expression of another gene
- 9:3:3:1 is the expected ratio of an F2 dihybrid cross with no epistasis

19
Q

Complementary Epistasis

A

(9:7), when genes work in tandem to produce a single product

20
Q

Duplicate Epistasis

A

(15:1), Genes encode same product or encode products that have the same effect in a pathway or compensatory pathways
- dominant allele at either locus gives rise to a wild-type phenotype
- Redundant system

21
Q

Dominant epistasis

A

(12:3:1), The ability of a dominant allele at one locus to override or mask the interacting allele(s) of a second locus

21
Q

Recessive Suppressor

A

mutant allele (i.e. the suppressor) of one gene reverses the mutant effect at another gene, resulting in wild type or near wild type phenotype
-13:3

22
Q

Recessive epistasis

A

(9:3:4), Ability of a recessive allele at one locus to override or mask the interacting alleles of a second locus

23
Q

Dominant suppression Epistasis

A

(13:3), Suppressor dominant gene has no mutant phenotype, only acts as a suppressor to inhibit the effect of another dominant allele