Week 2 Flashcards

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.

A

Fluorescent.

20
Q

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

A

Illumina.

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.

A

Sticky.

24
Q

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

A

Blunt.

25
Q

_________________ are enzymes that seal breaks in the sugar phosphate backbone, they can join blunt or sticky ends.

A

DNA ligases.

26
Q

________________ are enzymes that synthesize a new strand of DNA.

A

DNA polymerase.

27
Q

____________ are enzymes that help remove base stacking.

A

Topoisomerase.

28
Q

________________ are enzymes that remove RNA primers and ___________ adds the missing complementary bases.

A

Exonucleases, DNA polymerase.

29
Q

________________ is the process of copying DNA in a living organism.

A

Cloning

30
Q

____________ are short loops of bacterial DNA that bacteria use to exchange genes with one another, they can optimized by cloning DNA.

A

Plasmids.

31
Q

_______________ is the process of getting pieces of DNA into a bacterial cell.

A

Transformation.

32
Q

_____________ is the process of getting pieces of DNA into a eukaryotic cell.

A

Transfection.

33
Q

_______________ is the process in which DNA can be introduced into the cell.

A

Electroporation.

34
Q

Methods of transfection include:

A
  1. Virus infection.
  2. Electroporation.
  3. Cationic lipids.
  4. Microinjection.
35
Q

______________ 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.

A

Biolistics.

36
Q

______________ used to introduce DNA to alter the genetic sequence of a virus and use that virus to deliver genes. Modifies the viral genome.

A

Recombinant Viral-Mediated Gene Delivery.

37
Q

________________ are organisms that can be transfected with pieces of DNA integrated into the host genome.

A

Transgenic Organisms.

38
Q

__________________ is the process in which a specific mutation is generated at a specific site in the sequence.

A

Site-directed mutagenesis.

39
Q

___________ is the process of removing a protein.

A

Gene silencing.

40
Q

______________ are organisms that can take advantage of homologous recombination to delete a gene.

A

Knockout organisms.

41
Q

______________ exchanging a DNA sequence with another one with large, very similar ends. Occurs During meiosis in eukaryotes.

A

Homologous recombination.

42
Q

_______________ is the process in which gene expression is regulated, short stretches of mRNA are synthesized that are the __________ complement message.

A

RNA interference, reverse.

43
Q

___________ it is RNA interference but smaller.

A

siRNA.

44
Q

siRNA uses ___________ enzymes to induce assembly in a manner which prevents mRNA reading.

A

Dicer.

45
Q

CRISPR works in combination with the nuclease ___________ to cut both strands of DNA and leave them exposed.

A

Cas9.