ch 4 extensions of mendelian inheritance Flashcards

1
Q

mendelian inheritance

A

a pattern of inheritance that follows mendel’s laws; this pattern involves the transmission of eukaryotic genes that are located on the chromosomes found within the cell’s nucleus

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2
Q

simple mendelian inheritance

A

an inheritance pattern involving simple, dominant/recessive relationship that produces observed ratios in the offspring that readily obey mendel’s laws

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3
Q

wild-type alleles

A

an allele that is fairly prevalent in a natural population, generally found in more than 1% of the population; for polymorphic genes, there is more than one wild-type allele

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4
Q

genetic polymorphism

A

when two or more alleles occur in population; each allele is found at a frequency of 1% or higher

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5
Q

mutant allele

A

an allele that has been created by altering a wild-type allele by mutation

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6
Q

gain-of-function mutations

A

a mutation that changes a gene product so that it gains a new or abnormal function

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7
Q

dominant-negative mutations

A

a mutation that produces an altered gene product that acts antagonistically to the normal gene product; shows a dominant pattern of inheritance

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8
Q

haploinsufficiency

A

the phenomenon in which an individual has only a single functional copy of a gene and that single functional copy does not produce a normal phenotype; shows a dominant pattern of inheritance

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9
Q

incomplete penetrance

A

a situation in which an allele that is expected to cause a particular phenotype does not

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10
Q

expressivity

A

the degree to which a trait is expressed; for example, flowers with deep read have a high expressivity of the red allele

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11
Q

temperature-sensitive allele

A

an allele for which the resulting phenotype depends on the environmental temperature

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12
Q

incomplete dominance

A

a pattern of inheritance in which a heterozygous that carries two different alleles exhibit a genotype that is intermediate to those of the corresponding homozygous individual; a heterozygous may have pink flowers, whereas the homozygous have red or white flowers

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13
Q

overdominance (heterozygote advantage)

A

an inheritance pattern in which a heterozygous has greater reproductive success than either of the corresponding homozygous

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14
Q

multiple alleles

A

two or more alleles of the same gene found within a population

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15
Q

codominance

A

a pattern of inheritance in which two alleles are both expressed in the heterozygous condition; for example, a person with the genotype IA and IB has the blood type AB and expresses both surface antigens A and B

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16
Q

x-linked inheritance

A

an inheritance pattern in certain species that involves genes that are located only on the X chromosome

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17
Q

hemizygous

A

indicates that a male had a single copy of an x-linked gene; a male mammal is said to be hemizygous for x-linked genes

18
Q

x-linked recessive

A

an inheritance pattern in which a gene is found on the x-chromosome and the disease-causing allele is recessive relative to a corresponding dominant allele

19
Q

reciprocal cross

A

a pair of crosses in which the traits of the two parents differ with regard to sex; for example, one cross could be a red eyed female fly and a white eyed male fly the reciprocal cross would be a red eyed male fly and a white eyed female fly

20
Q

sex-linked genes

A

gene that is located on only one of the chromosomes

21
Q

y-linked genes (holandric genes)

A

genes (or alleles of genes) that are located only on the y chromosome

22
Q

pseudoautosomal inheritance

A

the inheritance pattern of genes that are found on both the x and y chromosomes; even though such genes are located physically on the sex chromosomes, their pattern of inheritance is identical to those of autosomal genes

23
Q

sex-influenced inheritance

A

an inheritance pattern in which an allele is dominant in one sex but recessive in the opposite sex

24
Q

sex-limited inheritance

A

an inheritance pattern in which a trait is only found in one of the two sexes (ie beard development)

25
sexual dimorphism
phenomenon in which the males and females of a species are morphologically distinct
26
lethal allele
an allele that may cause the death of an organism
27
essential gene
a gene essential for survival
28
nonessential genes
genes that are not absolutely required for survival although they are likely to be beneficial to the organism
29
conditional lethal alleles
an allele that is lethal, but only under certain environment conditions
30
temperature-sensitive (ts) lethal alleles
an allele that is lethal only in certain environmental temp range
31
semilethal alleles
lethal alleles that kill some individuals but not all
32
age of onset
the age at which symptoms of a disease first appears
33
pleiotropy
the multiple effects of a single gene on the phenotype of an organism
34
gene interaction
the phenomenon in which two or more different genes influence the outcome of a single trait
35
epistasis
an inheritance pattern where one gene can mask the phenotypic effects of a different gene
36
recessive epistasis
a form of epistasis in which an individual must be homozygous for either recessive allele to mask a particular phenotype
37
complementation
a phenomenon in which the presence of two different mutant alleles in the same organism produces a wild-type phenotype; usually happens because the two mutations are in different genes so the organism carries one copy of each mutant allele and one copy of each wild-type allele
38
gene modifier effect
an outcome in which the allele of one gene modifies the phenotypic effect of the allele of a different gene
39
gene knockout
in the case of diploid species, the condition in which both copies of a gene have been altered to an inactive form
40
gene redundancy
the phenomenon in which one gene compensates for the lost of function of another gene
41
paralogs
homologous genes within a single species that constitute a gene family