Chapter 9 - Mendel's Experience and Inheritance Flashcards

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1
Q

Genetics

A

Study of genes and their transmission from 1 generation to the next.

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2
Q

Inheritance

A

the passing down of genetic traits from generation to generation

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3
Q

Gene

A

unit of DNA that encodes for a protein
-portion of DNA that determines traits
-responsible for the expression of traits
-no pair
-eye color, hair color

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4
Q

Allele

A

a specific form of gene
-responsible for the variations
-pairs (always 2/gene)
-blue eyes, straight hair

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5
Q

Genome

A

sum total of all of an individuals DNA

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6
Q

Gene Locus

A

the location of a specific gene or pair of genes on the chromosomes
-pair of genes: always one copy is maternal and one is paternal

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7
Q

Homozygous

A

when 2 alleles of same gene are identical

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8
Q

Heterozygous

A

when 2 alleles of same gene are different

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9
Q

Genotype

A

the set of all alleles

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10
Q

Phenotype

A

physical characteristics

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11
Q

ALL alleles of same gene encode the same type of ____.

A

Protein

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12
Q

Dominant Alleles

A

alleles that mask the expression of others

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13
Q

Recessive Alleles

A

alleles that are masked by dominant alleles

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14
Q

Punnet Squares

A

predict what genotypes the offspring of 2 individuals will have

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15
Q

Dihybrid Crosses

A

genes of different chromosomes segregate independently of one another during gamete formation

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16
Q

Polygenic Traits

A

phenotypes determined by more than one gene
-skin color, eye color, foot size, height

17
Q

Height Genes

A

each height gene has a “short” allele and a “tall” allele
-tall alleles are dominant
-ratio of tall to short dictates height

18
Q

Polygenic - Eye Color

A

eye color depends on multiple genes
-each allele represents a specific color
-final eye color is the ratio of all dominant color alleles to homozygous recessive color alleles

19
Q

Mutations

A

changes in the nucleotide bases (nitrogen base pair) of our DNA that are different from the original DNA sequence
-some do not alter the protein sequence and are harmless, called silent mutations
-other mutations can slightly change the proteins but do not cause disease or otherwise harm the organism in which they are expressed; contribute to various alleles for normal phenotypes
-mutations that can cause disease or otherwise harm the organisms are called deleterious

20
Q

Types of changes to the nucleotides in the DNA sequence can include:

A

-deletions
-substitutions
-insertions

21
Q

Deleterious Mutations

A

result in non-functional or dysfunctional protein products
- central dogma: DNA dictates protein creation
-normal (non-mutated) allele is called the wild-type allele
-mutant alleles either dominant or recessive compared to the wild-type allele

22
Q

Phenylketonuria (PKU)

A

Homozygous Recessive Disorder
-requires both alleles to have a deleterious mutation
-wild-type allele is dominant, mutant allele is recessive
-single gene disorder = only takes mutation in one gene to cause disease
-heterozygous persons = “carriers” of PKU but are not affected themselves.
-phe = essential AA, requires PHA enzyme to break down (phenylamine hydroxylase) to turn into tyr which is another essential AA
-when a person can’t make PHA enzyme, decrease in tyr (which can be found in food), but also increases phe (causes behavioral issues, mental issues, disease)