2.5 Genetic variation and change Flashcards

(36 cards)

1
Q

multiple alleles

A

a gene that has more than two alleles

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2
Q

linked genes

A

genes found on the same chromosome. linkage increases the closer they are are and ones close together are more likely to be in the same gamete

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3
Q

homozygous

A

an organism which has two alleles that are the same (BB)

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4
Q

heterozygous

A

an organism which has two alleles that are different (Bb)

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5
Q

genotype

A

the genetic makeup of an organism

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6
Q

phenotype

A

the physical expression of a gene

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7
Q

allele

A

a variant of a gene which is inherited

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8
Q

lethal alleles

A

alleles that produce a phenotypic effect causing the death of an organism. it is caused by the mutation of an essential gene - causing an essential protein to no longer be produced functionally. if heterozygous, the organism will be a carrier (and most likely survive)

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9
Q

incomplete dominance

A

alleles which are mixed in expression ex. blue + yellow = green

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10
Q

co-dominance

A

when two alleles are identically dominant and are thus expressed equally
ex. blue + yellow = blue + yellow

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11
Q

monohybrid cross

A

a cross (punnet square) that involves only one gene
ex. eye colour

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12
Q

dihybrid cross

A

a cross (punnet square) that involves two different genes being inherited
ex. eye and hair colour

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13
Q

fillal

A

relating to an organisms child (the equivalent of “paternal” but for offspring)

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14
Q

pedigree chart

A

family trees showing the presence/absence of a trait

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15
Q

test cross

A

breeding an organism with an unknown genotype with one that is homozygous recessive

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16
Q

mutation

A

a permanent change to the DNA base sequence, it is the only way new alleles are made

17
Q

mutagens

A

environmental factors, such as UV light, which increases the likelihood of mutations

18
Q

neutral mutation

A

a mutation with neither positive or negative impacts

19
Q

silent mutation

A

no observable impact, usually because amino acid has not changed

20
Q

block mutation

A

changes to a segment of chromosome (could be several genes)
includes inversion, deletion, duplication and translocation

21
Q

inversion mutation

A

where sections of DNA swap places

22
Q

deletion mutation

A

where a section of DNA is removed

23
Q

duplication mutation

A

where a section of DNA is repeated

24
Q

translocation mutation

A

where a section of DNA is added from another chromosome

25
stop codon
a specific sequence which tells the ribosomes to stop making proteins. mutations can cause a stop codon to be made prematurely, leading the rest of the DNA "code" to be lost OR prolong the stop codon
26
point mutation
a small number of base pair changes
27
homologous chromosomes
two chromosomes that share the same structural features, such as size, banding pattern and centromere position. they also have the same genes at a specific loci position. one chromosome in each pair is from a parent
28
DNA
DNA is a polymer made of "deoxyribose" a nucleotide monomer. in eukaryotes, the DNA supercoils around a histone protein
29
non-favourable alleles
alleles that will be lost from the population because individuals possessing them will have reduced reproduction and survival
30
genetic drift
the change in allele frequency in a population due to chance events
31
genetic biodiversity
the range of all the alleles present in the gene pool. important to the survival of a species because the greater the range of alleles, the greater the variation within the population
32
favourable alleles
will be passed on to offspring
33
selection pressure
a biotic or abiotic factor which effects the survival of an organism and therefore influences reproductive success in a population. some members of the population will not survive and reproduce and thus will not pass on their genes into the next generation
34
template strand
the sequence of DNA that is used during the synthesis of mRNA
35
coding strand
the opposite strand directly corresponding to the mRNA sequence
36
tRNA
brings in the amino acids