Chapter 15 Flashcards

1
Q

law of segregation

A

the two alleles for each gene separate during independent assortment

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2
Q

law of independent assortment

A

alleles of genes on nonhomologous chromosomes assort independently during gamete formation

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3
Q

chromosomal theory of inheritance

A

states that Mendelian chromosomes have specific loci

o Also, it is the chromosomes that undergo segregation and independent assortment

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4
Q

wild type

A
red eyes (most common phenotype) found in drosophila (w+)
o	dominant trait
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5
Q

mutant type

A

traits that are alternative to the wild type

o w- white

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6
Q

X-Y system

A

sex of offspring depends on whether sperm cell contains X or Y chromosome

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7
Q

X-0 system

A

females have two x chromosomes (XX), males have one sex chromosome (X0)
• Sex is determined based on whether sperm carries X chromosome or no chromosome at all
• Grasshoppers, cockroaches, and beetles

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8
Q

Z-W system

A
sex chromosome present in egg, are either Z or W
•	Females- ZW
•	Males- ZZ
•	76 chromosomes
•	Birds, fishes, and insects
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9
Q

Haplo-diploid system

A

females develop from fertilized eggs and are thus diploid, males develop from unfertilized eggs and are haploid (males have no fathers)
• Bees and ants

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10
Q

SRY

A

“sex-determining region of Y”

o In absence of this region, gonads develop into ovaries

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11
Q

sex-linked gene

A

gene located on either sex chromosome

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12
Q

Y-linked gene

A

genes located on Y chromosome

• Passed down by father

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13
Q

X-linked gene

A

genes found on the X chromosome

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14
Q

hemizygous

A

when a male lacks a recessive allele from his mother

o One or more genes that have no allelic counterparts???

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15
Q

Hemophelia

A

x-linked recessive disorder marked by absence in factors involved in blood clotting
o Bleeding can cause severe damage
o Results from mutation on X chromosome
Below… irrelevant?
o Almost all of one X chromosome is inactivated during female embryonic development
o Consequently, males and females have the same dose of X-linked genes

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16
Q

Barr body

A

inactive X chromosome in a female
o Lies along the inside of a nuclear envelope
o Reactivated in ovaries to give rise to eggs so that each female gamete has an active X

17
Q

linked genes

A

genes located near each other on the same chromosome and which are inherited together

18
Q

genetic recombination

A

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

19
Q

parental types

A

when the offspring inherit a phenotype that matches either of the phenotypes of the parental (P) generation

20
Q

recombinant types/recombinants

A

offspring with new combinations of phenotype
o Results from random orientation of homologous chrom. at metaphase I of meiosis which leads to independent assortment of 2 unlinked genes

21
Q

crossing over

A

process that breaks the physical connection between specific alleles of genes on the same chromosome
o Accounts for recombination of linked genes

22
Q

genetic map

A

an ordered list of the genetic loci along a particular chromosome

23
Q

Sturtevant’s hypothesis

A

o Stated that the recombination frequency depends on the distance between genes on a chromosome
o Assumed crossing over was a random event
o Predicted that the farther two genes are, the higher the probability that a crossover will occur between them and therefore, the higher the recombination frequency

24
Q

recombination frequency

A

likelihood of recombination?
o The maximum value is 50% and occurs when two genes on a chrom. are so far apart crossover is basically guaranteed
• At this point, the genes are still considered genetically unlinked and assort independently (as if they were on different chromosomes).

25
linkage map
genetic map based on recombination frequencies
26
map units
how Sturtevant expressed the distance between genes | o 1 map unit was defined to equal a 1% recombination frequency
27
cytogenic maps
locate genes with respect to chromosomal features, such as stained bands
28
nondisjunction
o When members of a pair of homologous chromosomes do not separate properly during meiosis I o Or when sister chromatids fail to separate during meiosis II o Consequence: one gamete receives 2 copies of the same type of chromosome while another receives no copy o If occurs during embryonic development, aneuploidy condition passed on by mitosis
29
aneuploidy
when zygote has an abnormal number of particular chromosome
30
monosomic (aneuploidy)
when fertilization results in a gamete with a missing copy of a chromosome  Result: cell has 2n-1 chromosomes
31
trisomic (aneuploidy)
when chromosome is present in three copies in zygote  Result: cell has 2n+1 chromosomes  Ex: down syndrome
32
polyploidy
when organisms have more than 2 complete sets of chromosomes in all somatic cells o Can result from failure of 2n zygote to divide after replicating its chromosomes
33
deletion
when chromosomal fragment is lost | • Resulting chromosome is missing certain genes
34
duplication
when 1 of 2 things happens: • 1) When a detached fragment attaches to a nonsister chromatid of a homologous chromosome • 2) When a chromosome is missing certain genes and the deleted fragment becomes attached as an extra segment to a sister chromatid.
35
inversion
when a chromosomal fragment may reattach to the original chromosome but in the reverse orientation
36
translocation
chromosomal breakage that causes a fragment to join to a nonhomologous chromosome
37
Down syndrome
results from extra chromosome 21 (chrom. is present in 3 copies total) o Each body cell has 47 chromosomes o Results from nondisjunction during meiosis I
38
Genomic imprinting
variation in phenotype depending on whether allele is inherited from male or female parent o Occurs during gamete formation and is the result of silencing a particular allele of a set of genes o Offspring expresses only one allele of an imprinted gene- the one inherited from either the female or the male parent o In new generations old imprints are erased and chromosomes of developing gametes are newly imprinted according to the sex of the individual o Sometimes consists of methyl groups that are added o Methylation may silence the allele