[LEC] Genomes and Variants Flashcards

To completely know, understand, comprehend, and duplicate genomes and variants (77 cards)

1
Q

Proteins that contribute
to the organization of the chromosome. (bridging, wrapping, or bending activities)

A

Nucleoid-associated proteins (NAPs)

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2
Q

TorF: Bacterial genome is simpler compared to human genome, but
still has same level of packaging

A

True

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3
Q

Compact bacterial chromosome

A

Nucleoid

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4
Q

(in NAPs) Antiparallel coiled hinged domain (safety pin)

A

SMC COMPLEX

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5
Q

(in NAPs) Small protein sub-unit that
bridges your interconnecting
sites between genome

A

H-NS

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6
Q

(in NAPS) Alters and facilitates the formation of loops

A

IHF

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7
Q

(in NAPS) Causes interlinkage between
successive joints/parts of linear
DNA

A

HU

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8
Q

Wraps around genetic material of virus which is either RNA or DNA, but never both

A

Capsid

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9
Q

Capsule is made of lipids which is enclosed by the outer layer called:

A

Capsid

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10
Q

TorF: All genes (99.99%) are already discovered and known

A

FALSE: only 50%

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11
Q

Part of bacteriophage that contains the viral genome

A

HEAD - inserted into the bacteria

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12
Q

Virus that attacks bacteria

A

Bacteriophage

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13
Q

Part of bacteriophage that is the attachment point for the virus

A

TAIL

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14
Q

HUMAN GENOME consists of ____ nucleotide bases

A

3 BILLION

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15
Q

Largest human gene, found in X
chromosome, responsible for repair of muscle injury

A

DYSTROPHIN

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16
Q

TorF: We are 49.999% the same with other humans

A

FALSE - 99.99%

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17
Q

DNA packaging and the various packing capacities involved to fit eukaryotic DNA into the nucleus (order)

A

DNA > Histone > Nucleosome > Chromatin Fiber > Chromosome

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18
Q

TorF: Bacteria have NAPs, while Humans have nucleosomes

A

THRUE

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19
Q

Histones are positively charged

A

yes

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20
Q

Most diverse/variable histone

A

H2

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21
Q

Histone Linker protein

A

H1

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22
Q

Histone Octamers

A

H2A, H2B, H3, H4

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23
Q

Gene without histone, turned off

A

knockout gene

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24
Q

Animal Chromosome that has lateral loops that extrude from the chromomeres at certain positions.

A

LAMPBRUSH CHROMOSOME

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25
Appear at the meiosis stage in which the chromosomes resemble a series of beads on a string.
Chromomeres
26
TorF: Lampbrush chromosome is found in humans
FALSE: Urodele amphibians
27
Animal Chromosome that is usually found at the interphase nuclei of some tissue of the larvae of flies.
POLYTENE CHROMOSOME
28
TorF: Repetitive DNA are protein coding sequences
FALSE: Non repetitive are coding
29
DNA sequences that are unique; only one copy in a haploid genome.
NON REPETITIVE DNA
30
Types of Repetitive DNA
Introns Moderately Repetitive Sequences (Interspersed Elements-Repetitive Transposed Sequences, Tandem repeated DNA- VNTRs and STRs) Highly Repetitive Sequences
31
short sequences of DNA that have the ability to move to new locations in the genome; called selfish DNA or junk DNA
TRANSPOSONS
32
TorF: Retrotransposons are also transposons
FALSE: non-transposons, opposite
33
<500 base pairs long and may be present 500,000 times or more in a human genome (SINE OR LINE)
SINEs (SHORT INTERSPERSED ELEMENTS)
34
about 6kb (>6,000) in length and may be present 850,000 times in the human genome.
LINEs (LONG INTERSPERSED ELEMENTS)
35
Tandem repeats that are with 2-to 5-bp repeats and an array size on theorder of 10–100 unit
MICROSATELLITES
36
Tandem repeats that with 10-to 100-bp (usually around 15-bp) repeats and an array size of 0.5–30 kb
MINISATELLITES
37
Tandem repeats that are 15 to 100bp long and found within and between genes
VARIABLE NUMBER TANDEM REPEATS (VNTRs)
38
YES/NO : Satellite DNA (satDNA) are highly repetitive
yes
39
TorF satDNA has variable GC-rich repeat forms
FALSE- AT-RICH
40
Length of satDNAs?
150 to 400bp
41
YES/NO: Noncoding RNAs have been found to have NO functions
NO - important role in neuronal functions
42
also called dead genes
PSEUDOGENES
43
TorF: Pseudogenes may evolve functions in regulating expression of related genes and may regulate their parental genes, similar to long noncoding RNAs or microRNAs (miRNAs).
TRUE
44
CAUSES OF GENOME EVOLUTION (MUTATION)
>replication error or DNA damage >Substitution mutation
45
The second step in Genome Evolution
FIXATION OF MUTATION
46
random changes in the frequency of a mutational variant in a population
GENETIC DRIFT
47
TorF: Evolutionary rate is a combination of the mutation rate and the rate of fixation.
TRUE
48
What dictates the evolutionary pace of the organism?
1)Mutation and 2)Fixation of Mutation
49
TorF: Larger genomes are favored directly by selection as a way to cellular economization
FALSE - smaller genome
50
TorF: natural selection directly favors genome reduction and low G+C content in free-living prokaryotes living in low-nutrient environments.
TRUE
51
TorF: genes unnecessary for living in intracellular conditions are NOT maintained by selection and are lost in the course of evolution.
TRUE
52
Type of Genome Reduction that states that smaller genomes are favored directly by selection as a way to cellular economization
THE STREAMLINING HYPOTHESIS
53
Type of Genome Reduction that states that in populations undergoing constant bottlenecks and no recombination, genome reduction occurs through the accumulation of slightly deleterious mutations.
MULLER RATCHET
54
TorF: Modifications of some genes coded in the reduced genome could allow the endosymbiont to cope with the loss of otherwise essential genes
YES
55
A bacteria living inside a host that survives from the host's proteins
ENDOSYMBIONT
56
TorF: The number of genes correspond to the number of proteins present
FALSE- not necessarily correspond
57
TorF: The mitochondrial genome is from the fathernal lineage
FALSE- MATERNAL
58
No. of bps and genes in the mitochondrial genome?
BPs- 17000 genes- 32
59
Each DNA molecule is organized into discrete units called ___
Chromosomes
60
The total genetic information stored in the chromosomes are referred to as the ____
Genome
61
YES/NO The total chromosome count in a human is 46 autosomes and two sex chromosomes, XX for females and XY.
NO: 44 autosomes
62
Type of RNA splicing: only exon 1 and 2 are spliced, it will result to a truncated protein
INCOMPLETE SPLICING
63
Type of RNA splicing: exon 1, exon 2, and exon 3 spliced (pero kalahati lang ni exon 3)
CRYPTIC SPLICING
64
position or location of a gene in the genome.
LOCUS
65
“version” of a gene that is present at any given locus.
ALLELE
66
Mutation that occur in non germline tissues and are non-heritable (e.g. breast)
SOMATIC MUTA
67
Mutation present in egg or sperm and are heritable (e.g. cancer family syndrome)
GERMLINE MUTATION
68
TorF: Somatic mutation affects the whole body
FALSE - Germline mutation
69
Mutation or Polymorphism: <1% of population Carrier Diseased Point Mutation
MUTATION
70
Mutation or Polymorphism: >1% of population Not affected At risk of a disease SNPs
POLYMORPHISM
71
Type of Point Mutation: Purine to Purine
Transition
72
Type of Point Mutation: C to G
Transversion
73
Type of Point Mutation: G to A
Transition
74
Types of Deletion Mutations
Cystic fibrosis (most common) Duchenne muscular dystrophy
75
Mutation where the reading frame is altered
FRAME-SHIFT MUTATIONS
76
FRAME-SHIFT MUTATIONS are produced by:
deletions, insertions, or splicing errors
77
Unstable trinucleotide repeats (trinucleotide repeat expansion)
DYNAMIC MUTATIONS