ch 15 Flashcards

1
Q

chromosomal theory of inheritance

A

mendelian genes have specific loci (positions) along chromosomes and it is the chromosomes that undergo segregation and independent assortment

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2
Q

sex linked gene

A

a single gene located on either sex chromosome

ex. X-linked genes
3 options for females
only 2 options for males

Females
–  XNXN  normal 
–  XNXn  normal 
–  XnXn   colorblind
Males 
 –  XNY   normal 
–  XnY     colorblind 

certain notation: X^allele

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3
Q

homologous pair #23

A

sex chromosomes are not truly homologous

Y is much smaller than X and carries less genes

XX= female
XY = male
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4
Q

linked genes

A

two or more genes on the SAME chromosome that tend to be inherited together

genes located near each other on the same chromosome tend to be inherited together in genetic crosses

unlinked = not on same chromosome

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5
Q

X inactivation in females

A

almost all of one X chromosome in each cell in female mammals becomes inactivated during early embryonic development

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6
Q

wild type

A

displays normal phenotype

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7
Q

mutant phenotype

A

mutations in the wild type allele; displays unusual phenotype

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8
Q

recombination frequency formula

A

recombinants / # total offspring x 100%

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9
Q

nondisjunction

A

the members of a pair of homologous chromosomes do not move apart properly during meiosis I or sister chromatids fail to separate during meiosis II

one gamete receives two of the same type of chromosome and the other gamete receives no copy

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10
Q

aneuploidy

A

this results from nondisjunction; if either of the irregular gametes unites with a normal one at fertilization, the zygote will also have an abnormal number of a particular chromosome

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11
Q

Heterozygotes can be ______

A

carriers

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12
Q

Females are _____ of two types of cells;

which are what ?

A

mosaics, which is the presence of two or more populations of cells with different genotypes in one individual, who has developed from a single fertilized egg

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13
Q

What was model genetic system?

A

Drosophilia; form of a test cross

crossing over occurred because results weren’t 1:1:1:1
the rare flies were due to crossing over!

wildtype = normal

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14
Q

recombinant offspring

A

these are rare because they are from crossing over; this will be the smaller number or outcome amount

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15
Q

parental type offspring

A

these are more common and match the parents

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16
Q

What is the likely hood of crossing over occurring on a chromosome?

A
  • The closer together genes are on a chromosome, the less likely there will be a crossover because there is less space
  • Genes farther apart will have a greater chance of crossing over- more options because more space
17
Q

genetic map

A

o 1% = one map unit

o Maximum distance is 50%

18
Q

translocation

A

moves a segment from one chromosome to a non homologous chromosome

19
Q

Barr body

A

the inactive X in each cell of a female condenses into a compact object called a Barr body, which lies along inside of nuclear envelope

20
Q

law of independent assortment

A

alleles of genes on non homologous chromosomes assort independently

occurs during metaphase I and then they separate during anaphase I

21
Q

law of segregation

A

two alleles for each gene separate during gamete formation

22
Q

X-linked genes

A

the human x chromosome contains 1,100 genes

ex. hemophilia

23
Q

genetic recombination

A

production of offspring with combinations of traits that differ from those found in either P generation parent

24
Q

crossing over

A

accounts for recombination of linked genes

25
Q

linkage map

A

a genetic map based on recombination frequencies

26
Q

map units

A

one map unit = 1% recombination frequency

27
Q

genetic map

A

an ordered list of the genetic loci along a chromosome

max is 50%

28
Q

deletion

A

occurs when a chromosomal fragment is lost

29
Q

duplication

A

the “deleted” fragment may become attached as an extra segment to a sister chromatid

30
Q

inversion

A

a chromosomal fragment may also reattach to the original chromosome but in the reverse orientation

31
Q

What is the probability that a human male will inherit an X-linked recessive allele from his father?

A

0% because a son cannot receive an X chromosome from his father.

32
Q

A woman is a carrier for red-green color blindness, a sex-linked trait. Her husband is normal (not color-blind) for this trait. What are the chances that their newborn daughter will be red-green color-blind?

A

0% The father only has a single, normal allele.

33
Q

Consider a woman who is a carrier of a recessive X-linked allele for hemophilia. Which of the following possibilities could explain the presence of the hemophilia allele in her genotype?

A

Either her mother was a carrier or her father had hemophilia.

34
Q

what mechanism can break a linkage?

A

crossing over

35
Q

Morgan’s experiments using Drosophila examined the inheritance patterns of the white eyed phenotype. The results provided evidence that:

A

the gene for white eye is on the X chromosome

36
Q

____________ is a mechanism that breaks linkage between genes.

A

crossing over