Central Dogma in Molecular Biology Flashcards

(67 cards)

1
Q

producing 2 identical copies of the original DNA.

A

DNA replication

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2
Q

DNA replication occurs during what phase of the cell cycle before cell division.

A

S phase

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3
Q

must be accurately copied to ensure each daughter cells receives exact genetic information as of the parent cell.

A

DNA

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4
Q

synthesized a primer that will start the replication.

A

Primase

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5
Q

a short sequence of RNA with a 3’ end than can be elongated by DNA polymerase.

A

Primer

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6
Q

add new nucleotides to growing strand

A

DNA polymerase III

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7
Q

removes primer (since it is RNA) and replace by DNA

A

DNA polymerase I-

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8
Q

DNA pol III elongates the primer by adding new bases, growing the strand in a 5’ to 3’ direction

A

Leading strand-

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9
Q

DNA pol III adds nucleotides (backward direction) from the replication fork producing short segment called Okazaki fragments.

A

Lagging strand-

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10
Q

Lagging strand- replication fork producing short segment called

A

Okazaki fragments.

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11
Q

joins together or sealed the okazaki fragments by addition of phosphate group.

A

DNA Ligase-

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12
Q

Types of DNA repair mechanism

A

Base excision repair (BER)
Nucleotide excision repair (NER)
Mismatch repair (MMR)
Double strand break repair
Homology directed repair

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13
Q

It Repairs single base that undergone alkylation, deamination of oxidation.

A

Base excision repair

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14
Q

Various enzyme (glycosylase, endonuclease, polymerase and ligase) remove mutated base from the double helix (excision) and replaced it with a normal.

A

Base excision repair

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15
Q

These chemical process if not corrected can lead incorrect base pairing resulting in substitution or deletion of bases.

A

Base excision repair

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16
Q

Detects and repair distortion (bulky) to the DNA strand as result of environment such a sun UV light ad some chemotherapeutic drugs.

A

Nucleotide excision repair (NER)

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16
Q

DNA glycosylase detects damaged bases.

A

Base excision repair

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17
Q

causes bulky DNA adducts.

A

Thymine dimerization

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18
Q

Wide strand that contain the lesion is excise (remove) and DNA polymerase enzyme synthesized the new strand

A

Nucleotide excision repair (NER)

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19
Q

Repair spontaneous base–base mis pairs and small insertions–deletion loops generated during DNA replication or recombination

A

DNA mismatch repair (MMR)

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20
Q

recognizes the mismatch to be followed by recruitment of repair enzymes that excise incorrect sequence.

A

DNA mismatch repair (MMR)

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21
Q

DNA polymerase and ligase resynthesized new strand using the parental strand.

A

DNA mismatch repair (MMR)

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22
Q

Repair double stranded breaks (DSB)

A

Homologous recombination repair (HR)

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23
Q

The repair mechanism is active during S ang G2 phase.
Involves unwinding of the damaged DNA helix and invasion of the damaged strands into a homologous DNA duplex molecule.

A

Homologous recombination repair (HR)

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24
The sister chromatid or homologous chromosome is used as template for synthesizing new strand.
Homologous recombination repair (HR)
25
Also repair double strand breaks (DSB) It is active throughout the cell cycle. Error prone. Repair mechanism does not need homologous template
Non homologous end joining repair (NHEJ)
26
changes in the base sequence of DNA resulting to genetic variation among organisms, in the case of human it causes disease mostly are malignant condition.
Mutation
27
are cause by environment like radiation, UV light, carcinogens and internal factors such as spontaneous mutation.
Mutation
28
Extreme exposure to environment increases the rate of
Mutation
29
The process of transferring the genetic information from DNA to RNA.
Transcription
30
A particular gene is transcribed in response to the need of the cell.
Transcription
31
catalyzes by reverse transcriptase enzyme producing complimentary DNA (cDNA) from mRNA.
Reverse transcription-
32
located upstream contains TATA box, recognition site for transcription.
Promoter region
33
located downstream. Forms a hairpin-like strand signaling the end of transcription.
Termination region
34
structure of a gene is consist of a
Promoter region RNA-coding region Termination region
35
these are proteins that regulates transcription process (when to turn on and how much).
Transcription factors-
36
is a mark where RNA polymerase bind and start copying the DNA strand. In eukaryotes it is known as TATA box.
Promoter
37
The RNA polymerase unwinds the DNA exposing 10-20 bases at a time forming the transcription bubble. One strand is only needed for the transcription (template strand).
Elongation
38
Elongation in what direction
5' - 3'
39
The RNA pol stops moving on the DNA template after reaching the termination region.
Termination
40
The transcribed RNA is a single stranded complementary copy of one of 2 strands
Elongation
41
Transcription stops, transcribed RNA is release from the template strand.
Termination
42
RNA modifications (maturation of RNA) process occurs in ?
Nucleus
43
removal of introns(non-coding protein) and rejoining of exons (protein-coding gene). This process is catalyzed by
Splicing spliceosome.
44
A process of decoding biologic information from mRNA to synthesize a protein.
Translation
45
Translation occur in the?
Ribosome
46
Enzymatic process of amino acid side chain modification after their protein biosynthesis.
Post Translation modification
47
It result to protein diversity.
Post Translation modification
48
A molecular laboratory technique used in clinical diagnostics.
Polymerase chain reaction
49
An in-vitro amplification/replication of DNA/RNA fragments through a cycle of heating and cooling.
Polymerase chain reaction
50
Generates millions of copies of DNA after the process. Invented by MULLIS in 1983.
Polymerase chain reaction
51
Components of PCR
DNA template/fragment- from the sample Primer (synthetic) Taq DNA Polymerase Synthetic deoxynucleotide triphosphate- dNTPs Buffer
52
These are fragments of interest or the target DNA for amplification, serves as a template.
DNA fragments
53
are present in biological samples. They are need to be purified and isolated from the sample before the actual PCR.
DNA fragments
54
Single stranded DNA (10-30 nucleotides) synthesized chemically(synthetic primer).
PRIMERS
55
Serves as the starting point for the amplification.
PRIMERS
56
Adds dNTPs to the growing strand of DNA.
Taq DNA Polymerase
57
Extracted from Thermus aquaticus a bacteria that lives in hot springs a can withstand hot temperature (> 100 C).
Taq DNA Polymerase
58
Provide nucleotides during DNA amplification.
dNTP- Deoxynucleotide triphosphate
59
Polymerase chain reaction process
Denaturation Annealing Extension
60
At 94 C the double-stranded DNA melts and opens into two pieces of single-stranded DNA
Denaturation
61
At 54 C the primers pair up (anneal) with the single-stranded template.
Annealing
62
at 72 C DNA polymerase extends the primer by its polymerase activity by adding dNTPS.
Extension
63
Polymerase chain reaction process cycle repeat for?
25-40 times to make a million copies of DNA sequence.
64
A technique used for identification and quantification of RNA.
RT-PCR
65
is used to allow a single strand of RNA to be transcribe into a complementary strand of DNA (cDNA).
reverse transcriptase enzyme
66
used to detect and study many RNA viruses.
RT-PCR