Chapter 15 Flashcards

1
Q

Chromosome theory of inheritance

A

Mendelian genes have specific locations along chromosomes, and it is the chromosomes that undergo segregation and independent assortment
A specific gene is carried on a specific chromosome

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2
Q

Females have… Males have…

A

Homologous X chromosomes

One X and one Y

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3
Q

Wild type

A

The phenotype for a character most commonly observed in natural populations

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4
Q

Mutant phenotypes

A

Traits that are alternatives to the wild type

They are due to alleles assumes to have originated as changes/mutations

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5
Q

Each egg receives

A

One chromosome

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6
Q

The Y chromosome is much smaller than

A

The X chromosome

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7
Q

Sperm receives

A

Half of sperm receives X chromosomes and the other half receives Y chromosomes

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8
Q

Sex-linked gene

A

A gene located on either sex chromosome

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9
Q

Y-linked genes

A

Genes located on the Y chromosome

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10
Q

X-linked genes

A

Genes located on the X chromosome

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11
Q

Hemizygous

A

Describes X-linked genes

Instead of hetero and homo

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12
Q

Any male receiving the recessive allele from his mother will

A

Express the trait

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13
Q

The cells of females and males have

A

The same effective dose (one copy) of most X-linked genes

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14
Q

Barr body

A

The inactive X in each cell of a female condenses into a compact object
Lies along the inside of the nuclear envelope

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15
Q

Most of the genes of the X chromosome that forms the Barr body are

A

Not expressed

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16
Q

Females have a mosaic of two types of cells

A

Those with the active derived from the father and those with the active derived from the mother

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17
Q

After an X chromosome is inactivated

A

All mitotic descendants of that cell have the same inactive X

18
Q

The number of genes in a cell is

A
Greater than the number of chromosomes
Each chromosome (except Y) has hundreds or thousands of genes
19
Q

Linked genes

A

Genes located near each other on the same chromosomes end to be inherited together in genetic crosses
Genetically linked

20
Q

Genetic recombination

A

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

21
Q

Parental types

A

Inherit a phenotype that matches either of the phenotypes of the P (parental) generation
Matching offspring

22
Q

Recombinant types (recombinants)

A

Nonparental phenotypes

New combinations

23
Q

Crossing over

A

Breaks the physical connection between specific alleles of genes on the same chromosome
Accounts for the recombination of linked genes
Occurs while replicated homologous chromosomes are paired during prophase of meiosis I
A set of proteins orchestrates an exchange of corresponding segments of one maternal and one paternal chromatid

24
Q

Each pair of homologous chromosomes lines up independently of other pairs during metaphase I, and crossing over prior to that, during prophase I, can

A

Mix and match parts of maternal and paternal homologs

25
Genetic map
An ordered list of the genetic loci along a particular chromosome
26
The farther apart two genes are,
The higher the probability that a crossover will occur between them and therefore the higher the recombination frequency
27
The greater the distance between two genes,
The more points there are between them where crossing over can occur
28
Linkage map
A genetic map based on recombination frequencies
29
Map units
Distance between genes
30
Despite being on the same chromosome and being physically connected,
The gees are genetically unlinked; alleles of such genes assort independently, as if they were on different chromosomes
31
Nondisjunction
Occasional mishap 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 another gamete receives no copy Other chromosomes are distributed normally
32
Aneuploidy
A condition... If either of the aberrant gametes unites with a normal one at fertilization, the zygote will also have an abnormal number of particular chromosomes
33
Monosomic
Fertilization involving a gamete that has no copy of a particular chromosome will lead to a missing chromosome in the zygote... called for that chromosome
34
Trisomic
If a chromosome is present in triplicate in the zygote... called for that chromosome
35
Polyploidy
More than two complete chromosome sets in all somatic cells
36
Deletion
Occurs when a chromosomal fragment is lost | Affected chromosome is missing certain genes
37
Duplication
Deleted fragment may become attached as an extra segment to a sister chromatid, producing...
38
Inversion
A chromosomal fragment may also reattach to the original chromosome but in the reverse orientation, producing...
39
Translocation
Fragment joins a nonhomologous chromsome, rearrangement called...
40
Genomic imprinting
Variation in phenotype depending on whether an allele is inherited from the male or female parent
41
Genomic imprinting occurs
During gamete formation and results in the silencing of a particular allele of certain genes
42
Not all of a eukaryotic cell's genes are located on nuclear chromosomes, or even in the nucleus, some genes are located
In organelles in the cytoplasm | These genes are called extranuclear genes or cytoplasmic genes