BMSC 210 > Chapter 12 > Flashcards

Chapter 12 Flashcards

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1
Q

genetic engineering

A

the use of in vitro techniques to alter genetic material in the lab

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2
Q

First gene clone and purified from pigs?

A

insulin

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3
Q

Recombinant DNA technology

A

the artificial recombination of DNA from two organism

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4
Q

Restriction Endonuclease Enzymes

A
  • recognize specific DNA sequences and cut DNA

- essential for in vitro DNA manipulation and gene cloning

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5
Q

methylation

A

Cells must protect their own DNA from inadvertent destruction

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6
Q

Type II

A
  • cleave DNA within recognition sequence

- most useful for specific DNA manipulation

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7
Q

Type I

A
  • first discovered/purified
  • cuts DNA at random far from recognition sequence
  • little practical value
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8
Q

Type III

A
  • large
  • cleaves outside of recognition sequences
  • rarely used
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9
Q

How do structures of cleaved products differ?

A

3’ or 5’ overhang or blunt ends

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10
Q

Recognition sequences are usually….

A

4-8bp long

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11
Q

How are the 3 letters in REs designated?

A
  • first letter is genus RE isolated from
  • next two represent species RE isolated from
  • roman numeral indicated over of discovery in that species
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12
Q

Escherichia coli enzyme designation

A

EcoRI, EcoRV

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13
Q

Escherichia coli recognition sequence

A

I: G|AATTC
V: GAT|ATC

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14
Q

DNA fragments produced by EcoRI

A

5’ overhangs

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15
Q

DNA fragments produced by PstI

A

3’ overhangs

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16
Q

DNA fragments produced by SmaI

A

blunt ends

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17
Q

The nucleic acid sequence where EcoRI cuts

A

GAATTC

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18
Q

Molecules with complementary sticky ends can easily…

A

anneal or form H bonds

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19
Q

Ligation

A

by DNA ligase can rejoin two sugar phosphate backbones of DNA through covalent binding

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20
Q

After modification, DNA can no longer…

A

be cut by a RE

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21
Q

3 main steps of gene cloning

A
  1. isolation and fragmentation of source DNA
    - insertion of DNA fragment into cloning vector
    - introduction of cloned DNA into host organism
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22
Q

plasmids

A

natural vectors and have useful properties are cloning vectors

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23
Q

Why are plasmids useful

A
  • small
  • independent origin of replication
  • multiple copy # so multiple copies of cloned gene per cell
  • presence of selectable markers
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24
Q

Vector transfer to host can be accomplished by

A

chemical transformation of host cell, sometimes conjugation or transduction, or electroporation

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25
Essential features of plasmid pUC19
-ampicillin resistance, polylinker with multiple restriction enzyme cut sites, lacZ is fully functional even with presence of polylinker
26
pUC19 size
- small | - 2686 bp
27
Enzymes used for cloning
- restriction endonuclease - DNA ligase - reverse transcriptase - DNA polymerase
28
DNA ligase
catalyze joining of two strands between 5' phosphate and 3' OH of adjacent nucleotides
29
Reverse transcriptase
converts RNA into DNA
30
DNA polymerase
Mostly used for 5'3' polymerizing activity; may have 3'5' and 5'3' exonuclease activity
31
blue colonies
do not have vector with foreign DNA inserted
32
white colonies
have foreign DNA inserted
33
genomic library
a nearly complete/complete copy of an organisms genome contained as recombinant DNA plasmids or phages
34
To clone only expressed genes, libraries can be constructed using...
the organisms' mRNA
35
How is mRNA cloned
It cannot be cloned directly and is used as a template for retroviral reverse transcriptase
36
common host strains
E coli, bacillus subtitles, saccharomyces cerevisiae
37
Ideal hosts should be...
- rapid growth in inexpensive medium - nonpathogenic - capable of incorporating DNA - genetically stable in culture - equipped with appropriate enzymes to allow replication of the vector
38
E coli
- well developed genetics - many strains - best known bacteria - potentially pathogenic and periplasm traps proteins
39
bacillus subtilis
- easily transformed - nonpathogenic - secretes proteins - endospore formation simplifies culture - genetically unstable and genetics less developed
40
saccharomyces cerevisiae
- well-developed genetics - nonpathogenic - can process mRNA and proteins - easy to grow - plasmids unstable and will not replicate most bacterial plasmids
41
Agarose Gel Electrophoresis
- separates DNA molecules based on size | - uses electrical field to separate charged molecules; nucleic acids migrate towards positive electrode
42
Agarose gels can be stained with ___________ and DNA is visualized under _________.
ethidium bromide, UV light
43
The same DNA cute with different restriction enzymes will have ___________ banding patterns on an agarose gel.
different
44
RE map
a map of the location of restriction enzyme cuts on a segment of DNA
45
PCR
DNA replication in a test tube - DNA amplification | -rapid amplification in the # of copies of specific DNA sequences for further analysis
46
Applications of PCR
- determing DNA sequences - cloning a specific fragment - identifying DNA source from a crime scene - paternity determination - analysis of ancient DNA - organisms presence in a specimen
47
Steps in PCR amplification
- DNA denatured by heat - add DNA pol - Ad Taq pol - heat and cool many many many times in similar cycles
48
A variation of PCR
reverse transcriptase PCR
49
Nucleic Acid Hybridization
Base pairing of single strands of DNA or RNA from 2 different sources to give a hybrid double helix
50
nucleic acid probe
segment of single-stranded DNA used in hybridization and has a predetermined identity
51
How are nucleic acid probes created?
By cloning, synthesis, or denaturing a fragment of DNA
52
molecular beacon
label probes
53
Synthesized DNA is used for..
primers and probes, and in site directed mutagenesis
54
FISH
Fluorescent In Situ Hybridization; uses fluorescent probe attached to oligonucleotide
55
Southern Blot
a hybridization procedure where DNA is in the gel and probe is RNA or DNA
56
Northern Blot
RNA is in the gel; Radioactive probe to a specific gene to total RNA which is run on a gel
57
How to detect clones containing correct DNA inserts
- establish if cloning procedure worked - antibiotic resistance/blue-white screening - if cells express the foreign gene - look for specific DNA is the gene is not expressed
58
reporter genes
- encode proteins that are easy to visually detect and assay | - lacZ, luciferase, green fluorescent protein
59
gene fusions
promoters or coding sequences of genes of interest can be swapped with those of reporter genes to elucidate gene regulation under various conditions
60
site-directed mutagenesis
performed in vitro and introduces mutations at a precise location -can be used to assess activity of specific amino acids in a protein
61
cassete mutagenesis/knockout mutations
DNA fragments can be cut, excised, and replaced by a synthetic fragment
62
gene disruption/ insertional inactivation
When cassettes are inserted into a gene disrupting its function -may cause knockout mutations
63
knockout mutations
total loss of gene function; great for studying what genes do
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