Chapter 14_DV Flashcards

(50 cards)

1
Q

What is the ‘blending’ hypothesis in genetics?

A

The idea that genetic material from the two parents blends together.

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2
Q

What contradicts the blending hypothesis?

A

Everyday predictions, breeding experiments, and reappearance of traits after skipping a generation.

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3
Q

What is the ‘particulate’ hypothesis?

A

The idea that parents pass on discrete heritable units (genes) that retain their separate identities in offspring.

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4
Q

Who documented the particulate mechanism through experiments?

A

Mendel documented it through his experiments with garden peas.

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5
Q

What was Mendel’s approach to studying heredity?

A

He used a scientific approach, conducting carefully planned breeding experiments.

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6
Q

What advantages do pea plants offer for genetic study?

A

Distinct heritable features, controlled mating, short generation time, and large number of offspring.

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7
Q

What does a heritable trait refer to?

A

A trait passed from parent to offspring.

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8
Q

What is hybridization in Mendel’s experiments?

A

The process of mating two contrasting, true-breeding varieties.

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9
Q

What is the parental generation in Mendel’s experiments called?

A

The P generation.

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10
Q

What are the offspring of the P generation called?

A

The F1 generation.

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11
Q

What was the ratio of purple to white flowers in the F2 generation?

A

Approximately three to one.

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12
Q

What did Mendel call the trait that was expressed in the F1 hybrids?

A

Dominant trait.

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13
Q

What is a recessive trait?

A

A trait that is masked in the presence of a dominant trait.

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14
Q

What is a gene according to Mendel’s findings?

A

What Mendel called a ‘heritable factor’ is now known as a gene.

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15
Q

What are alleles?

A

Alternative versions of genes that account for variations in inherited characters.

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16
Q

What does it mean for an organism to be homozygous?

A

It has two identical alleles for a character.

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17
Q

What does it mean for an organism to be heterozygous?

A

It has two different alleles for a gene.

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18
Q

What is the phenotype of an organism?

A

The physical appearance of an organism.

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19
Q

What is the genotype of an organism?

A

The genetic makeup of an organism.

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20
Q

What is a testcross?

A

Breeding a mystery individual with a homozygous recessive individual to determine its genotype.

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21
Q

What is the law of independent assortment?

A

The law stating that each pair of alleles segregates independently of each other pair during gamete formation.

22
Q

What is a monohybrid cross?

A

A cross between individuals heterozygous for one character.

23
Q

What is a dihybrid cross?

A

A cross between individuals heterozygous for two characters.

24
Q

What does the multiplication rule in genetics state?

A

The probability that two or more independent events will occur together is the product of their individual probabilities.

25
What does the addition rule in genetics state?
The probability that any one of two or more exclusive events will occur is calculated by adding together their individual probabilities.
26
What is the significance of Mendel’s laws of segregation and independent assortment?
They reflect the rules of probability in genetic inheritance.
27
What is the relationship between genotype and phenotype in inheritance?
It is often more complex than predicted by simple Mendelian genetics.
28
What is the relationship between genotype and phenotype in inheritance patterns?
The relationship is rarely as simple as in Mendelian genetics ## Footnote Many heritable characters are not determined by only one gene with two alleles
29
What are the basic principles that apply even to complex patterns of inheritance?
Segregation and independent assortment ## Footnote These principles are foundational in genetics
30
What can cause inheritance patterns of a single gene to deviate from simple Mendelian patterns?
The following situations: * Alleles are not completely dominant or recessive * A gene has more than two alleles * A gene produces multiple phenotypes
31
What occurs in complete dominance?
Phenotypes of the heterozygote and dominant homozygote are identical
32
Define incomplete dominance.
The phenotype of F1 hybrids is somewhere between the phenotypes of the two parental varieties
33
What is codominance?
Two dominant alleles affect the phenotype in separate, distinguishable ways ## Footnote Example: Human MN blood group
34
What is an example of incomplete dominance in plants?
Snapdragon color ## Footnote Red and white parents produce pink hybrids
35
How do dominance/recessiveness relationships of alleles depend?
On the level at which we examine the phenotype
36
What is pleiotropy?
Most genes have multiple phenotypic effects
37
What is epistasis?
A gene at one locus alters the phenotypic expression of a gene at a second locus
38
Give an example of a polygenic trait.
Skin color in humans
39
What is the norm of reaction?
The phenotypic range of a genotype influenced by the environment
40
What is a pedigree?
A family tree that describes the interrelationships of parents and children across generations
41
What are carriers in genetics?
Heterozygous individuals who carry the recessive allele but are phenotypically normal
42
What is cystic fibrosis?
The most common lethal genetic disease in the United States, caused by a defective chloride transport channel
43
What is sickle-cell disease?
A genetic disorder caused by the substitution of a single amino acid in hemoglobin
44
What is achondroplasia?
A form of dwarfism caused by a rare dominant allele
45
What is Huntington’s disease?
A degenerative disease of the nervous system that appears later in life
46
What is multifactorial inheritance?
Inheritance patterns influenced by both genetic and environmental factors
47
What is the purpose of genetic counseling?
To provide information to prospective parents concerned about a family history of specific diseases
48
What is amniocentesis?
A procedure that removes liquid that bathes the fetus for testing
49
What is chorionic villus sampling (CVS)?
A technique that removes a sample of the placenta for testing
50
What is newborn screening?
Tests performed at birth to detect some genetic disorders