Exam 4 - Ch. 15 Flashcards

(59 cards)

1
Q

What is the C-value?

A

the total amount of DNA found in a cell

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2
Q

What are the two types of Prokaryotes?

A

bacteria and archaea

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3
Q

What is the C-value paradox?

A

In eukaryotes, where there is little correlation between DNA quantity and an organism’s perceived morphological complexity

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4
Q

What are the two phenomena that explain the C-value paradox?

A
  1. whole-genome duplications resulting in polyploidy (genome is doubled)
  2. the existence of large portions of an organism’s genome that are largely functionless from the cell’s viewpoint
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5
Q

What does Satellite DNA do?

A

the tandemly repeating sequences of DNA that are commonly used for DNA profiling

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6
Q

What do telomeres do?

A

they are the regions of repetitve DNA at the end of the chromosome, that protect against chromosomal deterioration

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7
Q

What do introns do?

A

they are the non-coding sequences within genes that are removed by RNA splicing

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8
Q

What do Non-coding RNA genes do?

A

they are the codes for RNA molecules that are not translated into proteins

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9
Q

What are gene regulatory sequences?

A

sequences involved in the process of transcription (ex: promoters, enhancers, and silencers)

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10
Q

Larger genomes have:

A

more DNA that codes for proteins

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11
Q

The size of a plant or animal’s genome is unrelated to its body size or phylogenetic position. True or false?

A

True

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12
Q

In complex organisms, RNA molecules transcribed from __________ regions of the genome have roles in regulating gene expression, so in other words, they do not code for _________.

A

noncoding regions, proteins

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13
Q

What do mobile genetics elements do, and how do they do that?

A

replicate and insert themselves into an organism’s genome regardless to the consequences to the organism, by hijacking the same cellular machinery that replicates and transcribes protein-coding DNA

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14
Q

What are mobile genetic elements sometimes called and why?

A

selfish genetic elements, because they are more focused on making copies of themselves

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15
Q

Mobile genetics elements can:

A
  1. can cause gene duplication elements
  2. can cause mutations in protein-coding regions, which alters the protein functions
  3. can rearrange genes in the host genome
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16
Q

Mobile genetic elements can disrupt the function of? What does this result in?

A

protein-coding genes, results in obvious changes to an organism’s phenotype

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17
Q

How much of the DNA sequence is derived from mobile genetic elements?

A

45%

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18
Q

Do unicellular organisms have mobile genetic elements in their genomes?

A

they often do not

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19
Q

Intergenic regions

A

space between coding genes in the eukaryotic genome

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20
Q

What makes up the intergenic regions?

A

mobile genetic elements and their remnants

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21
Q

What is the most predominant noncoding DNA found in eukaryotic genomes?

A

introns

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22
Q

Where do introns occur?

A

within the coding regions of genes

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23
Q

What are introns transcribed into?

A

mRNA

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24
Q

Unicellular eukaryotes typically have _ to _ introns per genome.

25
What is the average amount of introns in vertebrates?
5-8
26
Do prokaryotes have introns?
no
27
Is there any implied importance to the positions of introns?
yes
28
Just because MGEs could be considered parasitic, does this mean they are good or bad?
neither
29
Could mobile genetic elements be considered parasitic?
yes
30
Transposons
mobile genetic elements that can change their position within a genome
31
Retrotransposons
mobile genetic elements that leave a copy of themselves behind when they move
32
How do retrotransposons leave copies of themselves behind?
by converting RNA into DNA through reverse transcription
33
What happens if transposition occurs in the germ line?
it will be passed on to the host's offspring
34
Do host genomes have mechanisms to counter mobile genetic elements?
yes
35
What are the mechanisms used to defend against mobile genetic elements?
DNA methylation and RNA silencing
36
Methylation
attachment of methyl groups to nucleotides, which prevents the transcription of DNA into RNA, thus preventing retrotransposons
37
RNA interference/RNA silencing
short sequences of RNA that match a particular mobile genetic element, and silences the expression of it
38
Polyploidization
whole-genome duplication
39
Segmental duplication
duplication that affects smaller sections of the genome, can copy a single complete gene, a piece of a gene, or several genes
40
What are the molecular mechanisms that cause segmental duplication?
unequal cross-over between chromosomes during meiosis, and mobile genetic elements
41
Duplication events are often selectively _______. Why?
neutral, because it does not affect the phenotype
42
Does fixation typically occur by chance alone? What does this mean for duplications in the long run?
- No, neutral alleles rarely drift to fixation - most duplications are soon lost from a population
43
What are the steps taken to preserve duplicated genes?
1. a duplicated allele must rise to fixation in a population 2. one of those duplicates acquires a mutation that changes its function from A to B 3. one of the gene copies acquires a mutation that changes its function 4. the new allele contains one copy that performs the new function, and then a second copy that performs a new function
44
What is the reason for the preservation of a duplicated gene?
can be attributed to selection, the new function increases fitness
45
Neofunctionalization
the gene copy that mutates from the original acquires an entirely new function that by chance benefits the organism
46
What happens to each copy of a gene in neofunctionalization?
one copy continues to perform the ancestral function, while the other acquires mutations that give it a new function
47
What is the widely accepted mechanism for the preservation of duplicate genes?
neofunctionalization
48
Subfunctionalization
the ancestral gene has two different functions, meaning that after the ancestral two-function gene is duplicated, one copy performs the ancestral function A, while acquiring a mutation that inhibits the other ancestral function
49
What eventually happens to a gene in subfunctionalization?
The other copy acquires another mutation that inhibits the ancestral function B
50
Gene families
groups of anywhere from two to hundreds of genes that are all descendants of a single ancestor gene
51
What are gene families a result of?
repeated duplication events
52
All genes in a gene family typically have similar structures and functions, but they do not:
perform identical function
53
What was adaptive genetic variation generated by?
mutational processes
54
Adaptation from new mutation
if the alleles that encode a novel adaptive phenotype appear after a new selective challenge arises (selection causes a new mutation)
55
Adaptation from standing genetic variation
alleles favored by the new selective challenge are present at low frequency in the population before the challenge arose (mutation was neutral until selected for)
56
What is the neurotoxin that garter snakes possess?
tetrodotoxin, which block the movement of sodium ions across cell membranes, and result in paralysis
57
What is theory behind garter snakes being resistant to neurotoxin tetrodotoxin?
it is possible that the alleles conferring with the resistance were passed down from the common ancestor
58
How did the resistance for TTX arise in each species?
independently
59
What is the adaptive resistance to TTX in garter snakes an example of?
adaptation from new mutation