Test 2 Flashcards

(69 cards)

1
Q

True or False: Minimum gene number and size requirement are not related to organism complexity

A

False
The more complex, the higher minimum gene number AND size required

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2
Q

Gene size is proportional to gene number in prokaryotes or eukaryotes?

A

Prokaryotes, eukaryotes have introns and exons that affect genome size

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3
Q

Horizontal Gene Transfer (HGT)

A

transfer of DNA from one cell to another without cell division (same generation)

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4
Q

Vertical Gene Transfer (VGT)

A

transfer of DNA from one cell to another utilizing cell division (across generations)

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5
Q

Pathogenicity islands

A

segments of DNA that are present in pathogenic bacterial genomes but absent in nonpathogenic relatives (acquired via HGT)

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6
Q

Gene Family

A

Multiple copies of gene type but with slight variations (expression, function, etc.) that are similar enough to become family

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7
Q

How do you determine what an essential gene is?

A

Something that is found across organisms

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8
Q

What types of genes are unique to vertebrates?

A

Immune or nervous systems

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9
Q

50% of the human genome can be classified as:

A

repetitive DNA (transposons, introns, telomeres, centromeres, satellite sequences, etc.)

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10
Q

How much of the human genome is made of exons?

A

1%

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11
Q

Roughly how many proteins are in the human proteome?

A

50,000-60,000 proteins

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12
Q

Are introns longer or shorter than exons in humans?

A

Introns are longer in humans compared to plants that have smaller genes with shorter introns

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13
Q

Redundant genes

A

When there are two or more copies of a single gene, can lead to mutations in either that might not have detectable effects

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14
Q

scarce mRNA

A

large number of individual mRNA species, each present in very few copies per cell (most genes)

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15
Q

abundant mRNA

A

highly active, usually associated w/specialized function

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16
Q

housekeeping gene

A

high abundance, genes with standard or needed functions (ex. actin)
Important b/c measuring activity of genes need to make sure gene are not changing due to stress or other factors so a housekeeping gene will be used as a reference to see if activity level is stable

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17
Q

Synonymous mutation

A

mutation within a coding region that does NOT alter the amino acid sequence (aka silent mutation)

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18
Q

Nonsynonymous mutation

A

mutation within a coding region that DOES alter the amino acid sequence

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19
Q

positive selection

A

Non-synon/Synon > 1
make gene better version

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20
Q

negative selection

A

Non-synon/Synon < 1
changes/disrupt function of gene

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21
Q

Low heterozygosity of a gene

A

can indicate recent selective events

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22
Q

Where do most mutations in human genome occur?

A

Most likely to be in a regulatory element since exons are only 1% of human genome

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23
Q

Do synonymous or nonsynonymous mutations accumulate faster?

A

Synonymous mutations, since they don’t change function so it can be passed on easier vs nonsynonymous mutations that DO change function and can make it harder to pass the gene on

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24
Q

Orthologous genes

A

related genes in different species that have the same function. Made by speciation

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25
Paralogous genes
related genes in same species, not same function. Made by gene duplication
26
Pseudogenes
enough similarity but too many mutations leading to gene inactivation
27
Consensus sequence
Blast sequences against all other sequences to compare similarity, calculated by taking the most common base at each position, can help determine how long its been since divergence.
28
Codon bias
higher usage of one codon to encode for an amino acid in where there are several synonymous codes
29
Introns late hypothesis
earliest genes did not contain introns, later added to some genes Evidence: similar genes in closely related organisms have new introns in new locations
30
Introns early hypothesis
genes originated as interrupted structures, those now without introns have lost them in evolution Evidence: similar genes in distant organisms have similar locations; introns usually break up protein sub-domains
31
Exon shuffling
hypothesis that genes evolved by recombination of various exons encoding functional protein domains
32
Genome duplication
when polyploidization increases the chromosome number by a multiple of 2 (not common in animals)
33
Autopolyploidy
results from mitotic or meiotic errors within a species
34
Allopolyploidy
results from hybridization between 2 different but reproductively compatible species
35
Transposable elements
tend to increase in copy number when introduced to a genome, kept in check by negative selection and transposition regulation elements
36
Gene clusters
group of adjacent genes that are identical or related (physically next to one another on chromosome)
37
Dispersed gene family
Genes that are placed within the same family that are located on different chromosomes
38
Ribosomal RNA
increased demand in cell, evolved to have multiple copies Genes in genome (identical copies of one another) clustered together that when translated are made into rRNA
39
Identical genes
tandemly repeated to form one or more clusters
40
ribosomal DNA (rDNA)
transcriptional units alternate with non-transcribed spacers
41
Non-transcribed spacers
shorter repeating units whose number and length vary (repetitive but not identical)
42
Nucleolar organizer
region of chromosome carrying genes encoding rRNA
43
Nucleolus
denser region that stains darker b/c high transcriptional activity in region
44
Crossover fixation
hypothesis on how identical repeats are maintained consequence of unequal crossing over, allows mutation in one member of tandem cluster to spread through whole cluster --> continuous expansion and contraction of the number of genes in the cluster
45
Unequal crossing over
hypothesis on how identical repeats are maintained results from error in pairing and crossing over. one recombinant with deletion of genetic material and one with duplication
46
Concerted evolution
hypothesis on how identical repeats are maintained two or more related genes evolve together as if they were single locus
47
Gene conversion
if one gene mutated, cell will use other copy to do replication to maintain original sequence
48
Satellite DNA
short repeating DNA sequences, no coding function, do not interrupt coding sequences = not introns
49
CsCl gradient ultracentrifugation
Release DNA into solution and add CsCl and spin for hours, DNA will form band with certain density within density gradient (DNA ~1.7, RNA bottom, proteins top) DNA will have two bands upon closer inspection, and lower smaller band is satellite DNA
50
Euchromatin
most of the genome in interphase nucleus. Contain most of active or potentially active DNA. less tightly coiled than heterochromatin
51
In situ hybridization
used to identify the location of highly repetitive DNA
52
Human Minisatellite DNA in DNA Profiling
Differences in individuals on restriction fragments that contain short repeated sequences or using PCR
53
Chromosomes
unit of the genome carrying many genes
54
Chromatin
packaged DNA: DNA + proteins
55
Capsid
protein shell, formed by assembly of coat protein
56
Hairpin turn
when single stranded DNA or RNA can loop back on itself and bind ot itself, leaving a ring/hoop region at end where DNA/RNA remains unpaired
57
Rolling circle
genome replication mechanism, circular DNA helix is nicked, outer layer starts to unravel, DNA polymerase starts to replicate missing DNA but it cut off, creating copies of the genome ot insert into the capsid
58
Terminase
enzyme cleaving multimers using hydrolysis of ATP to provide energy to translocate DNA into empty viral capsid starting with cleaved end
59
Bacterial nucleoid
where genome is contained, multiple loops compacted by nucleoid associated proteins
60
Nucleoid associated proteins (NAPs)
associated with packaging DNA (--> gene expression) function in nucleoid architecture, domain topology, and gene regulation
61
Negatively supercoiled
supercoil is unwound, against turn of helix
62
Positively supercoiled
supercoil is tightly wound, with turn of helix
63
Scaffold
DNA loops around and attaches to scaffold at matrix attachment regions (sequences of DNA that attach to scaffold). no sequence conservation, unsure of how it signals DNA to attach at those points 1 scaffold = 1 chromosome
64
Endoreduplication
large chromosomes with many dna strands produced by successive replication of synapsed diploid pair of chromosomes replicas do not separate
65
H3 variant
marks where mitotic spindle attaches to centromere
66
CEN element
protein complex known as kinetochore allows a plasmid to segregate correctly at mitosis
67
CBF3
complex that binds to CDEIII and is essential for centromeric function
68
TRF2
protein that helps form t-loop
69