Genetic Engineering Flashcards

0
Q

What is Hybridization

A

Crossing organisms with different traits normally bigger and stronger than the parents
Ex-crossing a food plant with a non food plant that is resistant to a disease offspring have both traits

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1
Q

What is selective breeding

A

Humans choose the traits

Ex-Dogs

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2
Q

What is inbreeding

A

Crossing organisms with similar traits to maintain the desired characteristics

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3
Q

What are the cons of inbreeding

A

Greater risk of recessive genetic disorders because it is more likely that they will carry the allele
Ex-hemophilia in royal families

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4
Q

What is cull

A

Removing individuals you don’t want to produce

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5
Q

What is biotechnology

A

The application of technological processes to a living organism

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6
Q

What is a gene pool

A

All the genes and phenotypes of a specific breed

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7
Q

How do breeders increase diversity

A

Inducing mutations by using chemicals and radiation

Ex-drugs that will prevent chromosomal separation during meiosis can produce polyploid plants

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8
Q

What is genetic engineering

A

Involves making changes in DNA

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9
Q

How can DNA be extracted

A

It can be extracted from mast cells by a simple chemical process
We did this in the banana lab

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10
Q

What is transformation

A

The process in which a cell takes in dna from an organism outside the cell
-griffiths mice

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11
Q

What are plasmids

A

Small circular DNa molecules found in some bacteria

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12
Q

What is special about plasmids

A

They can replicate on their own

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13
Q

What do plasmids contain

A

They contain a sequence that promotes replication

Contain genetic markers

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14
Q

What are genetic markers

A

Genes that make it easy to distinguish the bacteria

Ex-anabiotic resistance genes are often used

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15
Q

Why do scientists cut DNA into fragments

A

Because it is too large to work with

-found answer in bacteria

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16
Q

What are restriction enzymes

A

Enzymes that cut DNA into fragments
There are hundreds of different types
Like little scissors
Each one cuts at a specific nucleotide sequence

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17
Q

Blunt vs sticky ends

A

DNA-ends end with the same complementation base: blunt end
DNA-ends end with one or more unpaired nucleotides: sticky end
There are enzyme available that cur sticky ends to blunt ends and vice versa, normally done after restriction enzymes did their job, in order to facilitate cloning.

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18
Q

What is the first step of making insulin

A

Take out plasmid DNA and human DNA

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19
Q

What is the second step of making insulin

A

Cut DNA samples with the same restriction enzyme

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20
Q

Is the third step of making insulin

A

Mix the fragments

-they join by base pairing

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21
Q

Why do you use the same restriction enzyme

A

It allows them to fit together

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22
Q

Do all of the plasmids take in the gene

A

No, others just glue back to itself

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23
Q

What is recombinant DNA

A

DNA containing two different sources of DNA

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24
What is the fourth step of making insulin
Place plasmids back into bacteria using a mechanical vector
25
What are mechanical vectors
Micropipette | Gene gun
26
What is a gene gun
Shoots microscopic bullets coated in DNA | Mostly used in plants because they can break the cell wall
27
What is the fifth step of making insulin
Allow the bacteria to produce
28
What happens each time the bacteria reproduce
It will copy the the inserted gene | It does this because DNA is universal
29
What is the end product of insulin production
A transgenic organism
30
What is a transgenic organisms
An organism with genes from other organisms
31
What is a polymerase chain reaction
A process used to make copies of DNA sample
32
What are the requirements of PCR
•Thermocycler-provides heat to separate the DNA strands •Primers-mall segments of DNA that bind to sample,DNA polymerase attaches to primers and begins copying DNA •nucleotides capable of making millions of copies in a short period of time
33
Inventor of PCR
Kary Mallis
34
Where was the DNA found that could withstand the pressure of the thermocycler
Yellowstone geysers
35
What is gel electrophoresis
The process that separates DNA fragments by size
36
What charge do DNA fragments have
Negative
37
What is the first step of gel electrophoresis
DNA is separated
38
What is the second step of gel electrophoresis
DNA is placed in wells on a gel plate
39
What is the third step of gel electrophoresis
Electric current is applied and negatively charged fragments migrate towards the positive pole
40
What is DNA fingerprinting
It analyzes sections of non coding DNA (introns) because they vary from person to person
41
Process of DNA fingerprinting
1-DNA cut by enzymes 2-gel run the same way 3-DNA probes are used to identify specific sequences Of nucleotides Southern blotting technique used to insert the probes
42
Result of DNA fingerprinting
A pattern of bonds that can be distinguished as belonging to a specific individual AKA DNA fingerprint
43
Used of DNA fingerprinting
Paternity tests and forensics
44
What is sequencing DNA
Scientist use PCR to make copies of unknown sample
45
What is special about sequencing DNA
Along with A,T,C,G, they also add special bases with a chemical die
46
What is the dye used for
The dye labeled basesterminate replication
47
What is the result of the dye
DNA fragments are different sizes
48
What is the last step in sequencing DNA
Gel electrophoresis can separate fragments by size
49
What is DNA MicroArray used for
It is used to study thousands of genes at once to compare their activity levels
50
What is the process of DNA MicroArray
Messenger RNA is removed, if the gene is active it will combined with the known genes of the MicroArray
51
What is an example of a genetically mutated plant
A plant that produces natural insecticides
52
What is the first step in cloning
The nucleus from egg is removed and a nucleus from a body cell is added
53
What is the next step of cloning
The new egg is placed in surrogate
54
What is an successful example of cloning
Dolly the sheep
55
What is a pro of cloning
It could help save endangered species
56
What is a con of cloning
It decreases genetic diversity
57
What is gene therapy
The process of changing genes that cause genetic mutations
58
What is used in gene therapy
Vectors are used to insert the normal Gene viruses are often used
59
What is some applications of gene therapy
Hemophilia and cystic fibrosis
60
What are the problems of genetic therapy
It decreases genetic diversity It conflicts with certain beliefs systems And the long-term effects have not been studied