Chapter 17 Flashcards

1
Q

Polygenic traits

A
  • influenced by many genes
  • each with small, additive effect
  • interactive
  • example: human height involves multiple genes -> growth hormones, cell division, metabolism etc.
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2
Q

epistasis

A
  • one gene alters the phenotypic expression of a 2nd gene

- often due to 2 or more different proteins involved in a single cellular function

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3
Q

epistasis example- lab skin & fur color

A
  • B locus- color of melanin pigment (B=black, b= brown)
  • E locus is epistatic to the B locus: prevents complete deposition of already-made pigment, but does not affect deposition in skin
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4
Q

discrete traits or discontinuous

A
  • clearly defined

- purple or white flowers, red or white eyes

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5
Q

Continuous or quantitative

A
  • majority of traits
  • heigh, skin color, number of apples on a tree
  • Polygenic- multiple genes contribute to phenotype
  • environment also plays a role
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6
Q

independent assortment

A

assumes genes are inherited independently of each other

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7
Q

non-independent assortment

A
  • genes on same piece of DNA are “linked”
  • tend to be inherited together
  • do not follow the law of independent assortment
  • linkage- when 2 genes are close on the same chromosome, they tend to be transmitted as a unit
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8
Q

non-independent assortment- fly example

A
  • morgan mated a homozygous wild-type female for body color and wing shape to a homozygous mutant male
  • female was gray body with straight wings (b+b+c+c+)
  • male was black with curly wings (bbcc)
  • mated F1 female with fly homozygous recessive for both traits (testcross) to produce F2
  • nonrecombinants or parental types- offspring’s traits have not changed from parental generations
  • recombinants or nonparental types- different combination of traits from parental generation
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9
Q

Morgan’s steps; non-independent assortment

A
  1. when different genes are located on the same chromosome:
    - traits determined by those genes are most likely to be inherited together
  2. due to crossing over during meiosis:
    - homologous chromosomes can exchange pieces of chromosomes and create new combinations of alleles
  3. the likelihood of crossing over depends on:
    - the distance between two genes
    - 2 genes farther apart ->more likely to cross over
    - 2 genes close together -> less likely to cross over
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10
Q

genetic mapping

A
  • if genes are linked, then the frequency that they end up in different offspring is the recombination frequency
  • use recombination frequency to determine how closely linked genes are
  • the closer they are linked, the lower the recombination frequency
  • one can make a chromosome map of the genes
  • one map unit is a 1% recombination frequency
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11
Q

extranuclear inheritance

A
  • what other organelles contain DNA?

- example: leaf pigmentation- maternal inheritance

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12
Q

extranuclear inheritance- Mitochondria

A
  • example: Neurogenic muscle weakness
  • mutations in mito gene that encodes ATP synthase
  • abnormalities of NS, eyes and muscles
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13
Q

epigenetic inheritance

A
  • genetic modification that does not change DNA sequence, effects gene expression
  • occurs during egg or sperm formation or early embryonic development
  • usually fixed throughout life
  • but not necessarily throughout several generations
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14
Q

X-inactivation in female mammals

A
  • only one X-chromosome active in each somatic cell
  • second condensed into Barr body
  • methylated, lies along inside of nuclear envelope
  • which one is silenced is random
  • dosage compensation-inactivation of an X gives equal expression of x-linked genes as seen in males
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15
Q

calico cats- X-inactivation example

A
  • patchy pattern due to inactivation of one X chromosome in each cell
  • X-linked gene for coat color
  • orange allele, X0and black allele, X8
  • heterozygous X0/X8 female will be calico
  • in early development, one of the 2 X chromosomes is randomly inactivated in each somatic cell
  • one or the other X is inactivated in different groups of cells, resulting in patches of black and organ fur
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16
Q

genomic imprinting

A
  • DNA segment marked in a way that effects gene expression
  • throughout an individuals life
  • single gene, part of chromosome, entire chromosome, or all chromosomes from a parent
  • imprinted genes do NOT follow Mendelian patterns of inheritance
  • offspring distinguished between maternally and paternally inherited chromosomes
  • offspring express either the maternal or paternal allele, not both