241 - 32, Cytoplasmic inheritance Flashcards

1
Q

cytoplasmic organelles behave differently and DO / DO NOT not obey Mendelian rules.

A

do not

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2
Q

Mitochondria are organelles that use ______ to produce energy efficiently

A

oxygen

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3
Q

Mitochondria have their own _____

A

genomes (DNA)

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4
Q

The human mitochondrial genome encodes __ genes: __ ribosomal RNA genes, __, tRNA genes (for protein synthesis), and __ proteins for energy metabolism

A

37, 2, 22, 13

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5
Q

The majority of mitochondrial proteins are made from ______ genes.

A

nuclear

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6
Q

_________ theory - Mitochondria (and chloroplasts) were derived from a symbiosis of an anaerobic eukaryotic cell and an aerobic prokaryotic cell. Many features of mitochondria resemble those of bacteria.

A

endosymbiant

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7
Q

Mutations disrupting the energy production process will affect the growth on non- fermentable ______

A

sugars

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8
Q

________ petite: The transmission of the phenotype follows the Mendelian pattern. These mutations affect nuclear genes that contribute to energy production in mitochondria.

A

segregational

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9
Q

______ petite: The mutant mitochondria are “recessive” to the wild-type ones.

A

neutral

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10
Q

In neutral petite, the four meioses inherit some . . . (type) mitochondria to restore their ability to grow on non-fermentable sugars.

A

wild-type

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11
Q

________ petite: the mutant mitochondria are “dominant” to the wild-type ones.

A

suppressive

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12
Q

the inheritance of mitochondria is from . . .

A

the mother

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13
Q

Mitochondrial diseases usually exhibit the following features (3)

A

maternal transmission
variable penetrance
expressivity

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14
Q

_________ component: stored in eggs as mRNA, proteins, and organization

A

maternal

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15
Q

________ component: newly transcribed materials from the embryonic genome

A

zygotic

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16
Q

The effects of mutations in maternal-effect genes are manifested in the ______

A

progeny (not the mothers)

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17
Q

_____ are the disease-causing agents for spongiform encephalopathy, mad cow disease.

A

prions

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18
Q

_____ alter cellular phenotypes through self-perpetuating changes in protein conformation and are cytoplasmically partitioned from mother cells to daughter.

A

prions

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19
Q

prions are partitioned from _____ to _____

A

mother to daughter

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20
Q

prions are susceptible to _______

A

proteases

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21
Q

______ are resistant to UV and nuclease treatment

A

prions

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22
Q

In yeast, _______ petites mutants that show Mendelian behaviour and result from mutations in mitochondrial genes located in the nucleus.

A

segregational

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23
Q

In yeast, ______ petites, which are recessive genotypes and result from the complete absence of mitochondrial DNA.

A

neutral

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24
Q

In yeast, ________ petites, in which most of the mitchondrial DNA is lost (60-99%), though what remains is often amplified.

A

suppressive

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25
________ ensure the proper segregation of genes during mitosis and meiosis
centromeres
26
Molecules that are not linked to chromosomes bearing nuclear centromeres behave differently during _______ and do not obey ______ rules
mitosis; Mendel's
27
_________ are involved in producing energy for the cell through oxidative phosphorylation
Mitochondria
28
nuclear DNA is ______ and mitochondrial _______ (shape)
linear; circular
29
nuclear DNA cells contain ___ copies of DNA, mitochondria cells contain _____ copies of DNA
2; 1000s
30
endosymbiont theory suggesting mitochondria are bacteria was proposed by _____ _______
Lynn Margulis
31
there are >_____(#) genes in nuclear DNA, ___ genes in mitochondrial
>30,000; 37
32
there are similar _____ compositions in membranes of bacteria and mitochondria (endosymbiont theory)
lipid
33
bacterial and mitochondrial genomes are ______ (shape) (endosymbiant theory
circular
34
bacteria and mitochondria have similar ____ (endosymbiant theory)
rRNA
35
In yeast, mitochondria are contributed by . . ., in humans . . .
yeast - both parents | humans - mother
36
Mutations in essential mitochondrial genes, or nuclear genes that affect mitochondrial function, results in a slow-growth phenotype on non-fermentable sugars (called _____)
petite
37
the high mutation rate of mitochondria suggests that the _____ mechanism IS / IS NOT as efficient as nuclear DNA
repair mechanism IS NOT
38
the high mutation rate of mitochondria suggests that there are many mutagenic ____ ________ around mitochondria
free radicals
39
yeast petite colonies are _____ than normal colonies
smaller
40
in segregational mutation in yeast petites the offspring will be . . .
1/2 petite, 1/2 normal
41
in neutral mutation in yeast petites the offspring will be . . .
all normal
42
in suppressive mutation in yeast petites the offspring will be . . .
all petite
43
myoclonic epilepsy and ragged red fiber disease is abbreviated . . .
MERRF
44
ataxia, deafness, dementia, and epileptic seizures are all due to . . .
MERRF (myoclonic epilepsy and ragged red fiber disease)
45
muscle fibers exhibit blotchy red patches resulting from the proliferation of aberrant (non-normal) _________ in what condition . . .
mitochondria; MERRF
46
in general, all the mitochondria in an individual are genetically _______
identical
47
________ - the existence of a uniform population of organelles within a cell or an individual
homoplasmy
48
________ - the existence of a variety of organelles within a cell or individual
heteroplasmy
49
proportion of mutant mitochondria determines the severity of the _____ phenotype
MERFF
50
HIGH / LOW energy requirement = least tolerant of mutant mitochondria
high
51
Tissues with LOW / HIGH energy requirements (e.g., skin) are only affected when the proportion of wild- type mitochondria is greatly reduced.
low
52
_______ component: stored in egg as mRNA, protein and organization
maternal
53
_________ (______) component: newly transcribed from the embryonic genome
embryonic (zygotic)
54
the _______ of the mother determines the inheritance of maternal effect genes
genotype
55
_____ diseases are called spongiform encephalopathies because of post mortem appearance of the brain large vacuoles in the cortex and cerebellum
prion
56
scrapie, TME, CWD, BSE (mad cow), CJ, GSS, FFI, Kuru all examples of _____ diseases
prion
57
______ resist inactivation by procedures that modify nucleic acids.
prions
58
UV treatment's effect on prions (scrapie)
none
59
the infectious prion PrP^Sc similarities to PrP^C are . . .
exact same
60
knockout mice lacking PrP are resistant to ______
prions
61
In Saccharomyces cerevisiae, a cross between a haploid suppressive petite mutant and a haploid wild type results in petite diploid progeny. This is because of . . .
deletions in the mtDNA
62
nonfunctional mutant mitochondria proliferation advantage in ________ petite because there are deletions in the mtDNA
suppressive
63
The transmission of prion is sensitive to the treatment of
protease
64
The maternal-effect mutation torso (tor) is recessive. In the absence of the torso protein product, embryogenesis is not completed (missing both head and tail structures). Consider a cross between a female heterozygous for the torso (tor+/tor-) and a male homozygous for the mutation (tor-/tor-).
all are normal