Week 2 Flashcards

(45 cards)

1
Q

____________ are nitrogenous bases that contain one ring.

A

Pyrimidines.

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2
Q

________________ are bicyclic nitrogenous bases that contain two rings.

A

Purines.

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3
Q

___________ are biomolecules that contain a nitrogenous base, a (deoxy)ribose sugar, and a phosphate group.

A

Nucleotides.

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4
Q

___________ are biomolecules that contain a nitrogenous base and a (deoxy)ribose sugar.

A

Nucleosides.

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5
Q

____________ are polymers of nucleotides.

A

Nucleic acids.

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6
Q

_____________ occurs when hydrophobic molecules aggregate within an oily pocket within a molecule.

A

Hydrophobic effect.

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7
Q

How many bases are found on one full turn of the DNA helix?

A

10

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8
Q

___________ are minor errors in the DNA sequence.

A

Mutations

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9
Q

____________ is the copying of DNA, it is bidirectional and semiconservative.

A

Replication.

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10
Q

Both the ________ strand and the ___________ strand are synthesized from the 5’ to 3’ direction.

A

Leading and Lagging.

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11
Q

Why can’t you synthesize both strands of DNA continuously?

A

Because you need to start from a certain position and DNA polymerase only works in one direction.

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12
Q

____________________ is the synthesis of short DNA fragments (up to 70 nucleotides) can be done by hand or robotically.

A

Solid phase nucleotide synthesis.

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13
Q

In solid phase nucleotide synthesis ___________ groups insure we are only adding 1 base at a time.

A

Protecting

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14
Q

________________ can be used to amplify millions of copies of a single fragment of DNA in a short period of time.

A

Polymerase Chain Reaction (PCR)

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15
Q

What does the PCR reaction mixture contain?

A
  1. Template DNA
  2. Primers
  3. Heat stable polymerase
  4. Deoxynucleotides.
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16
Q

What is the role of the primer in a PCR mixture?

A

It prevents the 2 strands of DNA from reattaching.

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17
Q

What are the steps for PCR?

A
  1. Denature
  2. Anneal oligonucleotide primers
    3.Extension of primers with taq polymerase.
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18
Q

What reaction mixture do we use for Sanger sequencing method?

A
  1. Template DNA
  2. Oligonucleotide or sequencing primer
  3. DNA polymerase
  4. Radiolabeled dideoxynucleotides.
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19
Q

______________ DNA sequencing that uses flourescently labeled dye terminator nucleotides.

20
Q

In ______________ sequencing genomic DNA is fragmented and ligated to adapters.

21
Q

____________ encoding is ligase based sequencing technology, it’s better at detecting single nucleotide polymorphism and is less expensive but slower than other sequencing techniques.

A

Two-Base Encoding.

22
Q

___________________ are enzymes that cut DNA.

A

Restriction Enzymes.

23
Q

____________ ends are easier to attach to other DNA sequences, more likely to have random reactions.

24
Q

___________ ends are harder to attach other sequences of DNA, less likely to have random reactions.

25
_________________ are enzymes that seal breaks in the sugar phosphate backbone, they can join blunt or sticky ends.
DNA ligases.
26
________________ are enzymes that synthesize a new strand of DNA.
DNA polymerase.
27
____________ are enzymes that help remove base stacking.
Topoisomerase.
28
________________ are enzymes that remove RNA primers and ___________ adds the missing complementary bases.
Exonucleases, DNA polymerase.
29
________________ is the process of copying DNA in a living organism.
Cloning
30
____________ are short loops of bacterial DNA that bacteria use to exchange genes with one another, they can optimized by cloning DNA.
Plasmids.
31
_______________ is the process of getting pieces of DNA into a bacterial cell.
Transformation.
32
_____________ is the process of getting pieces of DNA into a eukaryotic cell.
Transfection.
33
_______________ is the process in which DNA can be introduced into the cell.
Electroporation.
34
Methods of transfection include:
1. Virus infection. 2. Electroporation. 3. Cationic lipids. 4. Microinjection.
35
______________ is the technique in which DNA is put onto microscopic particles of gold or tungsten, and these particles are physically blasted into the cell using a pulse of helium gas. It is effective for genes that are hard to transfect.
Biolistics.
36
______________ used to introduce DNA to alter the genetic sequence of a virus and use that virus to deliver genes. Modifies the viral genome.
Recombinant Viral-Mediated Gene Delivery.
37
________________ are organisms that can be transfected with pieces of DNA integrated into the host genome.
Transgenic Organisms.
38
__________________ is the process in which a specific mutation is generated at a specific site in the sequence.
Site-directed mutagenesis.
39
___________ is the process of removing a protein.
Gene silencing.
40
______________ are organisms that can take advantage of homologous recombination to delete a gene.
Knockout organisms.
41
______________ exchanging a DNA sequence with another one with large, very similar ends. Occurs During meiosis in eukaryotes.
Homologous recombination.
42
_______________ is the process in which gene expression is regulated, short stretches of mRNA are synthesized that are the __________ complement message.
RNA interference, reverse.
43
___________ it is RNA interference but smaller.
siRNA.
44
siRNA uses ___________ enzymes to induce assembly in a manner which prevents mRNA reading.
Dicer.
45
CRISPR works in combination with the nuclease ___________ to cut both strands of DNA and leave them exposed.
Cas9.