MT2 Flashcards

1
Q

linkage

A

the association of two genes on the same chromosome

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2
Q

coupling configuration

A

arrangement of linked alleles in a dihybrid such that the two dominant
alleles are on a chromosome, the two recessive alleles are on the other chromosome (AB/ab)

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3
Q

repulsion configuration

A

arrangement of linked alleles in a dihybrid such that a dominant and a
recessive allele are together on each chromsome (Ab/aB)

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4
Q

cis dihybrid

A

a dihybrid in which the alleles are coupled (AB/ab)

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5
Q

trans dihybrid

A

a dihybrid in which the alleles are in repulsion (Ab/aB)

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6
Q

tetrad

A

(2) The four haploid product cells from a single meiosis (see the alternate definition provided
in Chapter 2)

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7
Q

octad

A

an ascus containing eight ascospores, produced in species in which the tetrad normally
undergoes a postmeiotic mitotic division

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8
Q

first division segregation

A

different alleles go into different nuclei at the first meiotic division
producing an MI division pattern of ascospores

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9
Q

second division segregation

A

different alleles go into different nuclei at the second meiotic division
producing an MII division pattern of ascospores

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10
Q

molecular marker

A

a site of DNA heterozgosity (difference), not necessarily associated with
phenotypic variation, used as a tag for a particular chromosomal locus

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11
Q

single nucleotide polymorphism (SNP)

A

change in a single nucleotide that can be located within a gene or intergenic regions

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12
Q

restriction enzyme

A

(restriction endonuclease) – an enzyme that will recognize specific target
nucleotide sequences in DNA and break the DNA chain at those points

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13
Q

simple sequence length polymorphism (SSLP)

A

the presence of different numbers of short or simple
repetitive elements at one particular locus in different homologous chromosomes

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14
Q

haplotype

A

a genetic class described by a sequence of DNA or of genes that are together on the same
physical chromosome (a chromosomal segment defined by the array of markers it carries)

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15
Q

complete dominance

A

alleles which, when combined in the heterozygote show a phenotype
indistinguishable from one of the homozygotes

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16
Q

haplosufficiency

A

one copy of the normal gene is able to confer a normal phenotype

17
Q

haploinsufficiency

A

one copy of the normal gene is unable to confer the normal phenotype

18
Q

codominance

A

alleles which, when combined in the heterozygote show phenotypic characteristics of
both homozygotes

19
Q

incomplete dominance

A

alleles which, when combined in the heterozygote show a phenotype
intermediate between the homozygotes

20
Q

lethal allele

A

an allele whose expression results in the death of the individual expressing it (may be
recessive or dominant)

21
Q

pleiotropic mutation

A

a mutation that affects several different phenotypic characteristics

22
Q

prototroph

A

an organism that will survive on minimal medium (carbon source, inorganic salts, water)

23
Q

auxotroph

A

an organism that will not survive on minimal medium, but whose growth depends on
supplementation of medium with a specific substance

24
Q

complementation test

A

a test for determining whether two mutations are in different genes (they
complement) or the same gene (they fail to complement)

25
Q

heterokaryon

A

cell with 2 nuclei in a common cytoplasm (results from fusing two haploid cells)

26
Q

epistasis

A

the phenotype of a mutant allele at one gene overrides the phenotype of a mutant allele at
another gene, such that the double mutant has the same phenotype as the first mutant

27
Q

suppression

A

a mutation in one gene can cancel the effect of a mutation in a second gene, resulting in
a wild type phenotype

28
Q

genetic redundancy

A

(duplicate genes) – Two independent genes that produce the same phenotypic
effect when present individually or when present together

29
Q

penetrance

A

the proportion of individuals with a specific genotype who show that genotype phenotypically

30
Q

expressivity

A

the degree to which a particular genotype is expressed in the phenotype

31
Q

chromosomes break and re-join during pairing, what is the visual evidence of that?

A

chiasmata

32
Q

crossing over occurs where?

A

chromatids (genes on the same chromosome)

33
Q
A