Modern Biology Flashcards - L4_ Genetics

(65 cards)

1
Q

field of biology devoted to understanding how characteristics are transmitted from parents to offspring.

A

Genetics

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2
Q

science of HEREDITY and VARIATION.

A

Genetics

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3
Q

The passing down of traits in the form of genes from parents to their children

A

Heredity

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4
Q

It is the difference in genes between individuals or groups of individuals.

A

Variation

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5
Q

a specific characteristic that varies from one individual to another.

A

Trait

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6
Q

different possibilities for a given trait.

A

Alleles

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7
Q

Every trait has at least how many alleles?

A

2

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8
Q

sequence of DNA that codes for a protein and thus determines a trait.

A

Gene

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9
Q

Father of Genetics

A

Gregor Mendel

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10
Q

He Identified specific traits in the garden pea and studied them from one generation to another.

A

Gregor Mendel

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11
Q

3 Laws of Mendel

A

Law of Dominance, Law of Segregation, Law of Independent Assortment

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12
Q

In this law, Hybrid offspring will only inherit the dominant trait in the phenotype.

A

Law of Dominance

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13
Q

In this law, two alleles for each trait separate when gametes form, and parents pass only one allele for each trait to each offspring.

A

Law of Segregation

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14
Q

It is when the two parent differ from one another by ONE trait

A

Monohybrid Cross

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15
Q

states that the alleles of different genes are inherited independently within the organisms that reproduce sexually.”

A

law of independent assortment

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16
Q

Independent assortment takes place during the process of ___

A

Meiosis

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17
Q

states that during a haploid. DIHYBRID CROSS (crossing of two pairs of traits), an assortment of each pair of traits is independent of the other.

A

law of independent assortment

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18
Q

The genetic make up of an organism

A

Genotype

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19
Q

The gene combination an organism has

A

Genotype

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20
Q

The way an organism looks

A

Phenotype

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21
Q

The physical characteristics of an organism

A

Phenotype

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22
Q

term used to refer to an organism that has two identical alleles for a particular trait

A

homozygous

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23
Q

term used to refer to an organism that has two different alleles for the same trait

A

heterozygous

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24
Q

When one allele is NOT completely dominant over another (they blend)

A

Incomplete Dominance

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25
It is when both alleles are expressed
Codominance
26
determines body traits
autosomes
27
Inability to distinguish between certain colors.
colorblindedness
28
A condition wherein blood won't clot
hemophilia
29
Graphic representation of how a trait is passed from parents to offspring
Pedigree
30
In a pedigree, what shape represents female?
Circle
31
In a pedigree, what shape represents male?
Square
32
In a pedigree, horizontal lines connecting a male and a female represent a ____
marriage
33
In a pedigree, this indicates a person has the trait
shaded circle or square
34
In a pedigree, partial shade represents a ____
carrier
35
When one gene mutation results in two or more seemingly unrelated observable traits.
Pleiotropy
36
describes a certain relationship between genes, where an allele of one gene hides or masks the visible output, or phenotype, of another gene.
Epistasis
37
It can be seen in the coat color of Labrador retrievers.
Epistasis
38
a picture of an individual's chromosomes. It can be used to diagnose chromosomal disorders.
Karyotype
39
a chromosome that is directly involved in determining the sex of the individual.
sex chromosome
40
47 chromosomes, extra chromosome at pair #21
Down syndrome
41
47 chromosomes, extra X chromosomes (XXY) that mainly affects boys, having low testosterone levels, underdeveloped muscles, sparse facial hair
Klinefelter's syndrome
42
only 45 chromosomes, missing a sex chromosome (X), Girls affected - short, slow growth, heart problems
Turner's syndrome
43
a stable, heritable change in the genetic material.
Mutation
44
Any change in the sequence of nitrogenous bases in the DNA, any mistake in the transcription of genetic information from DNA to RNA or pairing of codon and anticodon
Mutation
45
In this type of mutation, one base is incorrectly added during replication and replaces the pair in the corresponding position on the complementary strand.
Point mutation or single base pair substitution
46
an example of genetic disorder that illustrates a dramatic malfunction due to a change in just a single nucleotide in the DNA.
Sickle Cell Anemia
47
In this type of mutation, extra nucleotides are inserted into replicating DNA, often resulting in a frameshift.
Frameshift mutation by insertion
48
One or more nucleotides is "skipped" during replication or otherwise excised, often resulting in a frameshift.
Frameshift mutation by deletion
49
These are associated with random changes that cause errors when DNA is produced in the cell.
Spontaneous Mutation
50
Mutations may also be induced by environmental factors called ____
Mutagens
51
It may be in the form of radiation, chemicals, and microbial infection.
Mutagen
52
This gene mutation involves red blood cells being sickle shaped instead of round and cannot carry enough oxygen to the body tissues - heterozygous condition protects people from malaria
Sickle cell anemia
53
mucous builds up in the lungs
Cystic Fibrosis
54
deterioration of the nervous system - early death
Tay-Sachs Disease
55
an amino acid common in milk cannot be broken down and as it builds up it causes mental retardation - newborns are tested for this
Phenylketonuria (PKU)
56
gradual deterioration of brain tissue, shows up in middle age and is fatal
Huntington's Disease
57
variety of skeletal abnormalities
Dwarfism
58
In this process, a very few parent plants are chosen for breeding from a great number of individuals.
mass selection
59
may be the oldest form of plant breeding.
mass selection
60
crossing of two different but closely related strains.
Hybridization
61
the opposite of hybridization.
Inbreeding
62
Instead of crossing two parent plants, this involves self- pollination of a single parent.
Inbreeding
63
a condition, in which more than twice the haploid number of chromosomes are present,
polyploidy
64
Human diseases linked to point mutation/single base pair substitution
Albinism, Sickle Cell Anemia
65
Human Diseases linked to Frameshift mutation by insertion
One form of beta thalassemia