ch 4 extensions of mendelian inheritance Flashcards

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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
Q

sexual dimorphism

A

phenomenon in which the males and females of a species are morphologically distinct

26
Q

lethal allele

A

an allele that may cause the death of an organism

27
Q

essential gene

A

a gene essential for survival

28
Q

nonessential genes

A

genes that are not absolutely required for survival although they are likely to be beneficial to the organism

29
Q

conditional lethal alleles

A

an allele that is lethal, but only under certain environment conditions

30
Q

temperature-sensitive (ts) lethal alleles

A

an allele that is lethal only in certain environmental temp range

31
Q

semilethal alleles

A

lethal alleles that kill some individuals but not all

32
Q

age of onset

A

the age at which symptoms of a disease first appears

33
Q

pleiotropy

A

the multiple effects of a single gene on the phenotype of an organism

34
Q

gene interaction

A

the phenomenon in which two or more different genes influence the outcome of a single trait

35
Q

epistasis

A

an inheritance pattern where one gene can mask the phenotypic effects of a different gene

36
Q

recessive epistasis

A

a form of epistasis in which an individual must be homozygous for either recessive allele to mask a particular phenotype

37
Q

complementation

A

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
Q

gene modifier effect

A

an outcome in which the allele of one gene modifies the phenotypic effect of the allele of a different gene

39
Q

gene knockout

A

in the case of diploid species, the condition in which both copies of a gene have been altered to an inactive form

40
Q

gene redundancy

A

the phenomenon in which one gene compensates for the lost of function of another gene

41
Q

paralogs

A

homologous genes within a single species that constitute a gene family