Unit 2 - Final Review Flashcards

1
Q

Gregor Mendel

A

father of genetics. Studied pea plants.

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2
Q

Gene Pool

A

all the genes in a given population

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3
Q

Allele

A

alternate forms of a gene controlling a characteristic.
Found in the same position (locus) of homologous chromosomes

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4
Q

Pure

A

homozygous dominant or homozygous recessive

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5
Q

Heterozygous

A

genotype with 1 dominant and 1 recessive. Hybrid.

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6
Q

Genotype

A

alleles that make up a trait

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7
Q

Phenotype

A

observable characteristics of an organism.

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8
Q

Monohybrid cross

A

cross involving a single traits

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9
Q

Dihybrid cross

A

cross involving two traits

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10
Q

Generations naming

A

P1 = parents
F1 = first generation (filial)
F2 = 2nd generation

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11
Q

Mendels ratios (2 x heterozygous)

A

making two heterozygotes = 3:1 phenotype ratio, dominant: recessive

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12
Q

Mendel’s Laws of Heredity

A
  1. Law of Dominance
  2. Law of Segregation
  3. Law of Independent Assortment
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13
Q

Law of Dominance

A

In heterozygotes, the dominant alleles will mask the recessive allele; the dominant allele will be expressed exclusively.

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14
Q

Law of Segregation

A

during the formation of gametes, the two alleles responsible for a trait will separate. Offspring will receive one allele from each parent, which are recombined during fertilization = offspring genotype.

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15
Q

Law of Independent Assortment

A

alleles are randomly distributed to gametes. the allele that a gamete receives for one gene does not affect the allele that it receives for a different gene.

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16
Q

Genotypic ratios

A

homozygous dominant: heterozygous: homozygous recessive

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17
Q

Phenotypic ratios

A

dominant: recessive

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18
Q

test cross

A

performed between a homozygous individual and an unknown individual

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19
Q

Autosomal dominant

A

Both males and females are equally affected.
Unaffected parents cannot produce an affected child

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20
Q

x-linked recessive

A

Mostly males affected
No transmission of trait from father to son

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20
Q

autosomal recessive

A

Both males and females are equally affected.
Trait tends to skip generations
Unaffected parents can produce an affected child

20
Q

x-linked dominant

A

Affected sons must inherit from affected mother

21
Q

Pleiotropy

A

one gene affects more than one phenotypic characteristic

22
Q

Multiple alleles

A

more than two alleles for a specific trait (dominance hierarchy)

23
Incomplete dominance
having an appearance between phenotypes of the two parental varieties
24
codominance
both alleles are expressed at the same time. (e.g. blood type)
25
# of gametes that can be produced
2^n (where n = # of heterozygotes)
26
Mendel - dihybrid crosses
used this to develop the law of independent assortment
27
9:3:3:1
2 heterozygote traits x2
28
Selective breeding
used to improve domestic varieties of plants and animals
29
purebred (inbred)
similar phenotypes are selected for breeding
30
hybridization
desirable, but different traits are bred, creating new varieties
31
Epistatis
multiple genes affect a single trait (one gene may mask/interfere with the expression of another gene)
32
Complementary interaction
when 2 different genotypes interact to produce a phenotype that neither is capable of producing by itself.
33
T.H. Morgan
studied fruit flies. Discovered sex linked traits. Discovered that some genes do not segregate independently (linked genes)
34
Males cannot be ____ for sex linked traits
carriers/heterozygous
35
Barr bodies are...
small dark spots of chromatin that can be seen in somatic cells of female mammals during interphase.
36
Barr bodies (info)
females only need one of their x chromosomes to produce the proteins that their cell needs. One of the x chromosomes (random) goes dormant, becomes a barr body. Some will either display maternal/paternal x chromosome, so not all female cells will be identical.
37
Barr bodies (lethal genes)
heterozygous females who carry a lethal gene. Gene may only be active in 50% of cells.
38
Testes determining factor
lies on the y chromosome. When activated, it stimulates testes to start releasing male hormones.
39
Testicular feminizing syndrome (TFS)
XY embryo develops testes which secretes testosterone. Nearby tissues are insensitive to testosterone, and external female genitals form.
40
Linked genes
genes located on the same chromosome tend to be transmitted together. They move together during meiosis, resulting in fewer combinations of alleles
41
Non-recombinants/parental types
offspring that have the same genes as parents
42
Recombinants
offsprings with new combinations of alleles
43
crossing over
occurs during meiosis --> greater combinations
44
crossing over frequency
(recombinants/total offspring) x100
45
which genes are most likely to end up on the same chromosome?
those located closest to each other. The farther genes are, the more likely they will be affected by crossing over.
46
cross over % =
map unit
47
Transposons
specific segments of DNA that can move/jump along a chromosome
48
Gene Therapy
process by which defective genes are replaced with normal genes, in order to cure genetic diseases (gene insertion, gene modification, gene surgery)
49