Chapter 5: Population Genetics Flashcards

1
Q
  • the study of evolution from a genetic point of view
A

Population Genetics

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2
Q
  • a field of biology that studies the genetic composition of biological populations, and the changes in genetic composition that result from the operation of various factors, including natural selection
A

Population Genetics

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3
Q

population genetics it is the study of the allele frequency distribution and change under the influence of the four evolutionary processes: ______________________. It also involves the concepts of migration and isolation.

A

a. natural selection
b. genetic drift
c. mutation
d. gene flow

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4
Q
  • the percentage of alleles of a given type in a population
A

allele/gene frequency

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5
Q
  • a term of population genetics that is used in characterizing the genetic diversity of a species population, or equivalently the richness of its gene pool
A

allele/gene frequency

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6
Q

Levels of Biodiversity:

A

Ecosystem
Species
Genes

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7
Q

The amount of diversity at the genetic level is important because it represents the raw material for ________ and __________.

A

evolution and adaptation

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8
Q

More genetic diversity in a species or population means a greater ability for some of the individuals in it to_________________ in the environment.

A

adapt to changes

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9
Q
  • a change of the genetic structure of a population, and are brought by evolutionary factors
A

Evolution

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10
Q

Evolution type:

A

a. Microevolution
b. Macroevolution

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11
Q
  • changes in allele frequency of a population over time (genetic diversity)
A

Microevolution

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12
Q
  • large scale evolution of groups of species (speciation)
A

Macroevolution

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13
Q

Evolutionary Factors:

A

a. Natural Selection
b. Mutation
c. Genetic Drift
d. Gene Flow

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14
Q
  • is a mechanism of evolution
A

Natural Selection

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15
Q
  • organism that are more adapted to their environment are more likely to survive and pass on the genes that aided their success. This process causes species to change and diverge over time
A

Natural Selection

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16
Q
  • random changes of genetic information
A

Mutation

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17
Q
  • errors in DNA replication during cell division, exposure to mutagens or a viral infection
A

Mutation

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18
Q

Mutation is the ultimate source of ________

A

variation

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19
Q

Mutation often _______

A

lethal/detrimental

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20
Q

Type of Mutation:

A

a. Chromosomal Mutation
b. Gene Mutation

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21
Q
  • changes in structure as well as in number of chromosomes
A

Chromosomal Mutation

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22
Q

Chromosomal Types:

A

a. Euploidy
b. Aneuploidy
c. Chromosomal Aberrations

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23
Q
  • variation in complete sets of chromosome
  • refers to the changes involving the whole genome or entire set of chromosome
A

Euploidy

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24
Q

Euploidy Types:

A

a. Monoploidy
b. Diploidy
c. Polyploidy

25
Q
  • the number of sets of chromosome in a cell or an organism
26
Q
  • contains one half the normal number of chromosomes and is exhibited by monoploids (individuals having one set of chromosome)
A

Monoploidy (n)

27
Q
  • have two sets of chromosomes
A

Diploidy (2n)

28
Q
  • have 3 or more sets of chromosomes
A

Polyploidy (>2n)

29
Q
  • are organism with the cells containing 3 or more sets of chromosome or genomes (organisms with more than two genome0
A

Polyploids

30
Q
  • (3 sets or 3n;3x)
  • banana, apple, ginger, watermelon, citrus
31
Q
  • (4 sets or 4n;4x)
  • maize, cotton, potato, cabbage, tobacco, peanut
A

Tetraploidy

32
Q
  • (6 sets or 6n;6x)
  • wheat, kiwi, chrysanthemum
A

Hexaploidy

33
Q
  • variation in parts of chromosome sets
  • occurs when one or more chromosome of a normal set are lacking (hypoploidy) or present in excess (hyperploidy). This mostly causes abnormalities in human.
A

Aneuploidy

34
Q

Aneuploidy Types:

A

a. Monosomy
b. Trisomy
c. Tetrasomy

35
Q
  • (2n - 1)
  • the monosomics have only one chromosome instead of the 2 normal sets
36
Q
  • (2n +1)
  • the trisomics have one chromosome more than the normal 2 sets
37
Q
  • (2n + 2)
  • the tetrasomics have one chromosome represented 4 times
38
Q
  • the presence of more than two homologous chromosome sets
  • rare in humans
A

Polyploidy

39
Q
  • the presence of an abnormal number of chromosome
  • more common in humans
A

Aneuploidy

40
Q
  • changes in chromosome structure or structural changes involving parts of one or more chromosomes
A

Chromosomal Aberrations

41
Q

Chromosomal Aberrations are caused by ___________________ or chromatids

A

breaks in the chromosomes

42
Q

Kinds of Chromosomal Aberrations:

A
  1. Deletion or Deficiencies
  2. Duplication or Repeats
  3. Inversion
  4. Translocation or Interchange
43
Q
  • represent a loss of a segment or part of a chromosome. This may result to lethality or production of unique phenotypic effects on organism
  • e.g. Philadelphia 22 and Cri-du-chat syndrome
A

Deletion or Deficiencies

44
Q
  • occur when a section of chromosome is in excess of normal amount or there are extra copies of a part of a chromosome. This may result in the production of wild type of phenotypes
  • e.g. duplications of recessive alleles
A

Duplication or Repeats

45
Q
  • rotation of a chromosome segments to a full 180 degree
  • may result to partial or complete sterility of the organism
  • reverse the direction of a part of a chromosome
46
Q

Inversion types:

A

a. Paracentric Inversion
b. Pericentric Inversion

47
Q
  • occurs when the centromere is not included in the inverted segment
A

Paracentric Inversion

48
Q
  • occurs when the inverted segment includes the centromere
A

Pericentric Inversion

49
Q
  • occurs when a single breaks in two non-homologous chromosome produce an exchange of chromosome sections between them
  • occurs when part of a chromosome breaks off and attaches to another chromosome
  • may result to partial sterility or lethality in organism
A

Translocation or Interchange

50
Q
  • results from changes in an organism’s genotype or a change in the stored chemical information in DNA
  • changes to your DNA sequence that happen during cell division when your cells make copies of themselves
A

Gene Mutation

51
Q

Gene Mutation Types:

A

a. Point Mutation
b. Frameshift Mutation

52
Q
  • a genetic mutation where a single nucleotide base is changed, inserted, or deleted from a sequence of DNA or RNA
A

Point Mutation

53
Q
  • an insertion or deletion of a single base that change the reading frame of the entire subsequent sequence
A

Frameshift Mutation

54
Q
  • random fluctuation in the numbers of gene variations in a population
  • a change in the gene pool of a small population that takes place strictly by chance
A

Genetic Drift

55
Q
  • genes and other genetic elements of the next generation will be those of the lucky individuals, not necessarily the healthier or better individuals
  • most often observed in small population
A

Genetic Drift

56
Q
  • the transfer of alleles from the gene pool of one population to the gene pool of another population
A

Gene Flow/ Migration

57
Q

Main Factors Affecting Gene Flow/ Migration in Crop Species

A
  • Pollinators
  • Seed Dispersal
  • Breeding System
58
Q

Pollination (Biotic and Abiotic Agents)

A

(Zoophily):
- Hydrophily
- Anemophily
- Myrmecophily
- Ornithophily
- Malacophily
- Chiropterophily