Topic 15: Molecular Techniques Flashcards

1
Q

What is nucleic acid hybridization?

A

Base pairing of one strand of a nucleic acid to a complementary sequence on a strand from a different nucleic acid molecule

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2
Q

What is DNA sequencing used for?

A

Using the principle of complementary base pairing to determine the complete nucleotide sequence of DNA molecule

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3
Q

What do restriction enzymes do?

A

Cut DNA molecules at a limited number of specific locations

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4
Q

What is gel electrophoresis?

A

Separate out a mixture of nucleic acid fragments by size, charge or other physical properties using a gel made of a polymer as a molecular sieve

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5
Q

What is the purpose of PCR?

A

Obtain many copies of a desired gene

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6
Q

What are the 3 steps of PCR?

A
  1. Desaturation: heat briefly to separate DNA strands
  2. Annealing: cool to allow primers to form hydrogen bonds with ends of target sequence
  3. Extension: DNA polymerase adds nucleotides to the 3’ end of each primer
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7
Q

What is a nucleic acid probe?

A

A short, single stranded nucleic acid that can be either RNA or DNA used to detect the mRNA by nucleic acid hybridization, labeled with a fluorescent tag

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8
Q

What does FISH stand for?

A

Fluorescent in situ hybridization

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9
Q

What is fluorescent in situ hybridization?

A

Using a nucleic acid probe to hybridize specifically with any complementary sequences on the many mRNAs in cells where the gene is being transcribed

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10
Q

What is the purpose of FISH?

A

Determine where single genes are expressed by looking at mRNA

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11
Q

What does RT-PCR stand for?

A

Reverse transcriptase polymerase chain reaction

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12
Q

What are the 5 steals of making cDNA from mRNA?

A
  1. Reverse transcriptase added to mRNA
  2. Reverse transcriptase makes first DNA strand using mRNA as template
  3. mRNA degraded
  4. DNA polymerase synthesizes second DNA strand
  5. Results in cDNA
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13
Q

What is cDNA?

A

Complementary DNA made from mRNA that lacks introns

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14
Q

What are the 3 steps of RT-PCR?

A
  1. cDNA synthesis
  2. PCR amplification
  3. Gel electrophoresis
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15
Q

What is the purpose of RT-PCR?

A

Compare gene expression between samples

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16
Q

What is a DNA microarray?

A

Tiny amounts of large number of single-stranded DNA fragments representing different genes fixed to a glass slide in a grid of dots

17
Q

What is the purpose of DNA microarray assays?

A

Analyze expression of many genes

18
Q

What are the 6 steps of a microarray assay?

A
  1. Isolate mRNA from normal cell and tumor cell
  2. Prepare cDNA w fluorescent tag
  3. Separate cDNA into single strands and add to microarray
  4. Fluorescent strands anneal to complementary sequences
  5. Wash unhybridized cDNA strands
  6. See color
19
Q

What is RNA sequencing?

A

Sequence the cDNA samples from different tissues in order to discover which genes are expressed

20
Q

What are the 5 steps of RNA sequencing?

A
  1. Isolate mRNA samples
  2. Cut into shorter fragments
  3. Convert into cDNAs
  4. Sequence cDNA
  5. Map cDNA onto genome of species in question
21
Q

What is Sanger sequencing?

A

Using chain-terminating dideoxynucleotides during DNA replication

22
Q

What is SDS-PAGE used for?

A

Separate proteins on the basis of their size or charge

23
Q

How does SDS-PAGE work?

A

Using gel electrophoresis, proteins will move to anode or cathodes, then we can identify the presence of separated proteins

24
Q

What is Southern Blotting used for?

A

Detect a specific DNA sequence in a sample

25
Q

What is a chromosome painting used for?

A

Compare different chromosomes present between a abnormal and normal sample