Chapter 10 Flashcards

(46 cards)

1
Q

Diploid cell

A

Contains two sets of chromosomes with one inherited from each parent

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2
Q

Autosomes

A

The chromosomes that are the same for both sexes

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3
Q

Sex chromosomes

A

Determines each person’s sex
Female- XX
Male- XY

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4
Q

Homologous pair

A

Pair of chromosomes that have the same sequence of genes in the same positions

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5
Q

Meiosis

A

specialized form of cell division that occurs in diploid cells and gives rise to haploid cells

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6
Q

Haploid cells

A

contain just one set of chromosomes

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7
Q

Gametes

A

Haploid cells in humans. Sperm and egg cells.

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8
Q

Fertilization

A

Unites the gametes from two parents producing the first cell of the next generation

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9
Q

True breeding

A

Self fertilization always produced offspring identical to the parent plant

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10
Q

Hybrids

A

Plant Offspring mixed

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11
Q

Dominant allele

A

One that exerts its effects whenever it is present

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12
Q

Recessive allele

A

One whose effect is masked if a dominant allele is also present

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13
Q

Genotype

A

Expresses the genetic makeup of an individual and it is written as a pair of letters representing the alleles

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14
Q

Homozygous

A

Two identical alleles, meaning that both parents contributed the same gene version

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15
Q

Heterozygous

A

Two different alleles for a gene

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16
Q

Phenotype

A

Observable characteristics

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17
Q

Wild type allele, genotype, or phenotype

A

The most common form or expression of a gene in a population

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18
Q

Mutant allele, genotype, or phenotype

A

Variant that arises when a gene undergoes a mutation

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19
Q

P generation

A

(Parental) first set of individuals being mated

20
Q

F1 generation

A

Offspring of P generation

21
Q

F2 generation

A

The offspring of the f1 plants and so on

22
Q

Monohybrid cross

A

A mating between two individuals that are bother heterozygous for the same gene

23
Q

Punnett square

A

Diagram that uses the genotype a of the parents to reveal which allele combinations the offspring may inherit

24
Q

Testcross

A

A mating between an individual of unknown genotype and a homozygous recessive individual

25
Law of segregation
Mendels law that states that the two alleles of each gene are packaged into separate gametes. Which means that they move apart from each other during gamete formation
26
Dihybrid cross
A mating between individuals that are each heterozygous for two genes
27
Law of independent assortment
Medes proposal that states that during gamete formation the segregation of the alleles for one gene does not influence the alleles for another gene
28
Product rule
States that the chance that two independent events will both occu equals the product of the individual chances that each event will occur
29
Linked genes
Genes carried on the same chromosome; they are therefore inherited together. They do not assort independently during meiosis
30
Linkage group
Collections of genes that tended to be inherited together
31
Crossing over
An exchange of genetic material between homologous chromosomes during prophase 1.
32
Parental chromatid
Inherited by most offspring which retains the allele combination from each parent
33
Recombinant chromatid
Mix of maternal and paternal alleles
34
Linkage maps
Diagrams of gene order and spacing on chromosomes
35
Incomplete dominance
The heterozygote has a third phenotype that is intermediate between those of the two homozygotes
36
Codominance
Two different alleles are fully expressed in the phenotype
37
Pleiotropy
One gene has multiple effects on the phenotype. Arises when one protein is important in different biochemical pathways of affects more than one body part or process
38
Epistasis
Interaction that occurs when one genes product affects the expression of another gene
39
Sex-linked
Phenotypes that affect one sex more than the other
40
Y-linked
Few disorders linked to the Y chromosome
41
X-linked
Most human sex linked traits are x-linked, controlled by genes on the X chromosome
42
X inactivation
A cell shuts off all but one X chromosome in each cell. This process happens early in the embryonic development of a mammal
43
Autosomal dominant disorder
Expressed in heterozygotes and therefore typically appears in every generation
44
Autosomal recessive disorder
Requires that a person receive the disease causing allele from both parents.
45
Pedigree charts
Depict family relationships and Phenotypes for determining the mode of inheritance
46
Chromosomes
Long strange of DNA associated with proteins