Mendelian Genetics Flashcards

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1
Q

What is Mendel’s first law?

A

Alternative versions of a gene account for variations in inherited characters

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2
Q

What is Mendel’s second law?

A

Each character is independently inherited during gamete formation - each pair of alleles of a given gene are independently inherited from alleles at a different gene locus

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3
Q

Causes of deviations from Mendelian ratios

A
Epistasis
Incomplete dominance
Co-dominance
Co-dominance and multiple alleles
Lethal alleles
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4
Q

What is the difference between co-dominance and incomplete dominance?

A

In co-dominance heterozygote expressed in both forms - offspring looks like both parents at once
Incomplete dominance the heterozygote forms an intermediate phenotype - looks like a blend of both parents

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5
Q

What is pleiotropy?

A

When one gene influences 2 or more phenotypic traits

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6
Q

What is allelic heterogeneity?

A

A similar phenotype produced by different alleles of the same gene

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7
Q

What is locus heterogeneity?

A

A similar phenotype is produced by mutations at different gene loci

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8
Q

What is incomplete penetrance?

A

Not all individuals carrying a deleterious gene express the associated trait

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9
Q

What is linkage?

A

When particular gene loci are inherited jointly

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10
Q

Who discovered linkage?

A

Bateson and Punnet

Soon after 1900

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11
Q

What is recombination frequency?

A

A measure of how often recombination occurs between genes, measured as the fraction of offspring that inherit recombinant proteins

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12
Q

What is recombination frequency measured in?

A

centiMorgans (cM)

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13
Q

How do recombination frequencies determine where genes are relative to each other on a chromosome?

A

Recombination is less likely between genes that are closer, because there is less DNA between them

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14
Q

Why don’t gene mapping recombination frequencies always add up to 100%?

A

Double crossing over can occur

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15
Q

What is another name for a sex chromosome?

A

Allosome

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16
Q

What is X inactivation?

A

The inactivation of one of the two copies of the X chromosome in all female mammals. Happens during embryonic development

17
Q

What does the inactivated X chromosome become?

A

It condenses into a compact object called a Barr body. Most of its genes aren’t expressed and it lies alongside the nuclear envelope

18
Q

Why does X-inactivation not cause colourblindness?

A

The X chromosome is inactivated on a cell-by-cell basis - any daughter cell from one of the original embryonic cells will have the same X chromosome inactivated. As the eye comes from several different cells, some will have one X chromosome inactivated whilst others will have the other one inactivated

19
Q

How is mitochondrial DNA transcribed?

A

Like in prokaryotic cells with the production of polycistronic RNA (multiple genes on a single RNA molecule)