Heredity Flashcards

(59 cards)

1
Q

Character

A

A heritable feature in an organism

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2
Q

Trait

A

Variants of a character

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3
Q

True-breeding

A

A scenario where self-pollination always produces the same organism

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4
Q

P generation

A

True-breeding parental generation

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5
Q

F1 generation

A

Direct hybrids of true-breeding generation

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6
Q

F2 generation

A

Self-pollination of F1 generation

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7
Q

Dominant trait

A

A trait that is expressed over the recessive trait

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8
Q

Alleles

A

Alternative version of genes

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9
Q

Somatic cell

A

Body cell (non-sex cell)

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10
Q

Law of segregation

A

Two alleles for a character segregate during meiosis and arrive at different gametes

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11
Q

Homozygous

A

Pair of identical alleles

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12
Q

Heterozygous

A

Pair of different alleles (dominant one is expressed)

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13
Q

Phenotype

A

Physical appearance of a gene

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14
Q

Genotype

A

The genetic makeup

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15
Q

Testcross

A

A cross between recessive and an unknown organism to determine if the genotype is homozygous dominant or heterozygous

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16
Q

Monohybrid cross

A

Cross of two organisms that are hybridized for one trait (3:1 phenotypic ratio)

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17
Q

Dihybrid cross

A

Cross of two organisms that are hybridized for two traits (9:3:3:1 phenotypic ratio)

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18
Q

Law of independent assortment

A

Pairs of allele segregates independently of other pairs during gamete formation

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19
Q

Complete dominance

A

Heterozygotes exhibit no phenotypic trace of the recessive allele

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20
Q

Incomplete dominance

A

Heterozygotes have a mixture, or blending, of both alleles

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21
Q

Codominance

A

Heterozygotes exhibit both alleles at once

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22
Q

Tay Sachs disease

A

Disease with improperly functioning enzymes that lead to lipid accumulation in the brain; requires two alleles to manifest, but just one allele produces mediocre enzymes

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23
Q

Blood types

A

A, B, AB, O (describing surface carbs of a blood cell)

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24
Q

Pleiotropy

A

A condition where a gene is affected by multiple phenotypes

25
Epistasis
Phenotypic expression of one gene alters expression of a second gene
26
Polygenic inheritance
Phenotype is influenced by multiple genes
27
Multifactorial genes
Character influenced by genetic and environmental factors
28
Pedigree
Family tree describing traits of parents and descendants
29
Carriers
Heterozygotes who carry recessive alleles for a condition without expressing them
30
Cystic fibrosis
A disease preventing proper chloride ion transport in certain cells, causing thick mucus buildup
31
Sickle cell disease
A condition resulting in warped blood cells which cannot hold oxygen well
32
Sickle cell trait
The heterozygotic condition of sickle cell disease; results in some sickled and some regular blood cells
33
Huntington's disease
A late-onset disease that is passed onto offspring well before it manifests
34
Amniocentesis
Fetal testing using cultured amniotic cluid
35
Chorionic villus sampling
Fetal testing using cultured placenta tissue
36
PKU
A disorder that prevents breakdown of phenylalanine
37
Benefits of Drosophila in experiments
Short generation time, plenty of offspring, four pairs of chromosomes
38
Sex-linked gene
A gene present on a sex chromosome
39
Systems of sex chromosomes
X-Y: gamete in sperm dictates sex Z-W: gamete in egg dictates sex X-0: males have one sex chromosome Haploid-diploid: females are diploid, males are haploid
40
SRY
A gene on the Y chromosome that causes testes to form
41
Hemizygous
Describes a male with one allele present on the Y chromosome
42
Barr body
Condensed remnant of inactivated X chromosome
43
Linked genes
Occur near each other on the same chromosome
44
Recombinants
Offspring with different traits from the parents
45
Recombination frequency
Percent of offspring with recombinant type
46
Crossing over
Produces recombination
47
Linkage map
A representation of recombination frequencies
48
Nondisjunction
Failure of homologous chromosomes to separate
49
Aneuploidy
Abnormal number of a single chromosome
50
Monosomy
A chromosome is missing from a pair
51
Trisomy
A chromosome is added to a pair
52
Polyploidy
An entire set of chromosomes is replicated
53
Deletion
Chromosome fragment is lost
54
Duplication
Chromosome fragment is duplicated
55
Inversion
Chromosome segment is reversed
56
Translocation
Chromosome segment moves to another, non-homologous chromosome
57
Trisomy 21
Down's syndrome, results in developmental delays and physical aberrations
58
Klinefelter syndrome
XXY, sterile male sex organs
59
Turner syndrome
Monosomy X, sterile female sex organs