Genetics and Inheritance Flashcards

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1
Q

sum total of all of its DNA, even though not all of that DNA codes for proteins

A

genome

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2
Q

DNA sequences that code for one or more specific proteins are called

A

genes

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3
Q

the study of DNA and genes and their transmission from one generation to the next.

A

genetics

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4
Q

what happens just before egg and sperm are formed so that the genes we inherit
are also different from our siblings?

A

the genes reshuffle

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5
Q

variations on genes are essential for

A

evolution

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6
Q

are identifiable in cells only just before cell division.

A

chromosomes

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7
Q

before cell division, each chromosome can be identified by its

A
  • character size
  • centromere location
  • distinct banding pattern
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8
Q

A composite display of all the chromosomes of an organism

A

karyotype

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9
Q

1-22nd chromosome

A

autosome and homologous chromosomes

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10
Q

23rd chromosome

A

sex chromosome

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11
Q

The sex chromosomes look different from each other and function differently because

A

they carry different genes

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12
Q

Humans inherit how many of each pair of autosomes and how many sex chromosomes from each parent, giving us two copies of each gene.

A

1; 1

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13
Q

may exist between any pair of autosomes.

A

small differences in DNA sequence

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14
Q

Sequence differences that occur within genes thus, producing alternative versions of genes

A

Alleles

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15
Q

If an individual possesses two identical alleles of a particular gene, the person is said to be ______ for that gene

A

homozygous

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16
Q

A person who has two different alleles of a gene is

A

heterozygous

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17
Q

an individual can only inherit how many alleles even if there are more than two alleles of a particular gene in the human population?

A

2

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18
Q

Where did these different alleles come from?

A

millions of years of mutations of cells destined to be sperm or egg. and because they did not cause the cell to be nonviable, they continued.

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19
Q

all the various genes and their alleles in the human population are known as the

A

human gene pool

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20
Q

Your complete set of alleles

A

genotype

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21
Q

the observable physical and functional traits that characterize you.

A

phenotype

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22
Q

Your phenotype is determined not only by the alleles you inherit from your parents (your genotype) but also by

A

environmental factors and lifestyle

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23
Q

When gametes (sperm and eggs) are formed in the parents, each gamete receives only ___ of the parents’ two alleles.

A

1

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24
Q

described many of the fundamental principles of inheritance through a number of experiments involving controlled breeding of garden peas.

A

Gregor Mendel

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25
Q

Most do not confer a distinct advantage or disadvantage to the homozygous recessive person.

A

recessive alleles

26
Q

These alleles no longer code for a specific essential protein because their nucleotide sequence has been altered slightly from the dominant form.

A

Alleles that result in the loss of functionality of proteuins

27
Q

In principle, the frequency of truly harmful recessive alleles in a population is kept in check by the

A

occasional premature death of homozygous recessives

28
Q

Inheritance of two copies of a harmful recessive allele may result in

A

miscarriage of a fetus

29
Q

refers only to how an allele behaves in combination with a recessive allele
in a heterozygote.

A

dominant allele

30
Q

states that the alleles of different genes are distributed to egg and sperm cells independently of each other during meiosis

A

law of independent assortment

31
Q

the heterozygous genotype results in a phenotype

that is intermediate between the two homozygous phenotypes.

A

incomplete dominance

32
Q

both gene products are equally expressed

A

codominance

33
Q

Inheritance of phenotypic traits that depend on many genes

A

polygenic inheritance

34
Q

distributed to egg and sperm cells independently of each other during meiosis.

A

alleles of different genes

35
Q

Many alleles for different traits are often inherited together because

A

they are physically joined on the same chromosome.

36
Q

the closer they are located to each other on the chromosome the more likely they are to be inherited together.

A

linked alleles

37
Q

How often two linked alleles are inherited together is

clue: the more crossing-over occurs, the less likely the linked alleles will be inherited together

A

directly proportional to how close together they are and inversely proportional to how often crossing-over occurs

38
Q

technique on mapping the positions of genes by studying how often particular linked alleles are inherited together,

A

linkage mapping

39
Q

three major sources of genetic variability as a result of sexual reproduction:

A

● Independent assortment of alleles located on different chromosomes
● Partial shuffling of linked alleles as a result of crossing- over between autosomes
● Random fertilization of an egg by a sperm

40
Q

Why is the sperm of the father the determinant of the sex of the offspring?

A

Females have two X chromosomes and will donate one of them to the offspring, whereas males have an X and a Y chromosome, only one of which is donated to the offspring. If the male donates a Y chromosome, the fertilized egg has an X and a Y chromosome and will develop into a male.

41
Q

more likely to display any recessive trait found on the X chromosome, not just those that cause disease.

A

males

42
Q

In sexually reproducing animals in which the Y chromosome determines maleness, who have a homologous pair of X chromosomes?

A

females

43
Q

refers to inheritance patterns that depend on genes located on the sex chromosomes.

A

sex-linked inheritance

44
Q

Inheritance if the gene is located only on the X chromosome

A

x-linked inheritance

45
Q

inheritance if the gene is located only on the Y chromosome

A

y-linked inheritance

46
Q

apparently influence differentiation of the male sex organs, production of sperm, and the development of secondary sex characteristics, but not much else.

A

y-chromosome genes

47
Q

Hemophiliacs lack a blood-clotting factor that is encoded by

A

an x-linked gene with 2 alleles

48
Q

Testosterone strongly stimulating the expression of

the baldness allele, in effect converting it from a recessive to a dominant allele in males is an example of?

A

sex-influenced phenotype

49
Q

one not inherited with the sex chromosomes per se but influenced by the actions of the genes on the sex chromosomes.

A

sex-influenced phenotype

50
Q

People express inherited genetic disorders caused by defective recessive alleles only if they

A

get 2 of the recessive alleles

51
Q

human inherited disease in which homozygous recessive individuals are unable to
make an enzyme that is needed for the normal metabolism of phenylalanine, an amino acid.

A

Phenylketonuria

52
Q

PKU is caused by mutation of the gene

A

Chromosome 1

53
Q

Chromosome 1 is responsible for

A

producing the enzyme phenylalanine hydroxylase.

54
Q

Treatment of PKU requires limiting

A

dietary intake of Phenylalanine

55
Q

enzyme deficiency disease, this one caused by a recessive gene located on chromosome 15

A

tay-sachs

56
Q

Individuals homozygous for the recessive allele in Chromosome 15 are unable to make an enzyme that is responsible for the metabolism of a particular type of lipid,

A

sphingolipid

57
Q

Without this enzyme, the _______ accumulates in brain cells, causing cerebral degeneration

A

sphingolipid

58
Q

marked by progressive nerve degeneration leading to physical and mental disability and death.

A

Huntington’s disease

59
Q

HD is called a

A

Dominant-Lethal Allele

60
Q

are by their nature uncommon because they tend to eliminate themselves from the population, especially if they cause disease before the affected individual’s reproductive years.

A

dominant-lethal alleles