3.8.4 Gene Technologies Flashcards

1
Q

Determining the genome of simpler organisms allows

A

The sequences of proteins that derive from the genetic code of the organism to be determined

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2
Q

Why can’t genome knowledge by easily translated into proteome

A

Non-coding DNA and regulatory genes

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3
Q

Recombinant DNA tech involves

A

Transfer of DNA fragments from one organism or species to another

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4
Q

Genetic code, transcription translation mechanisms are

A

Universal

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5
Q

What can you do with transferred DNA

A

Translate into cells in transgenic organism

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6
Q

In vivo method to amplify DNA

A

DNA insert attached to plasmid
Plasmid + Gene cut with same restriction enzyme to create complementary sticky ends Fragments incubated with plasmids
Base pairing takes place
Joined with DNA ligase which forms phosphodiester linkages

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7
Q

What do restriction enzymes do

A

Cuts DNA into gene-sized pieces

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8
Q

How is reverse transcriptase used to amplify DNA

A

Remove mRNA from cell
Add reverse transcriptase
Convert RNA into DNA
Forms double stranded DNA
PCR amplifies DNA

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9
Q

Uses of genetic fingerprinting

A

Analysing DNA fragments that has been cloned by PCR + determining genetic relationships + genetic variability in a population
Forensic science
Medical diagnosis
Plant + animal breeding

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10
Q

Uses of DNA probes

A

Locate specific alleles of genes
Screen patients for heritable conditions, drug responses, health risks

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11
Q

What can be used to detect genetically modified cells in organisms

A

Marker genes

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12
Q

What is meant by recombinant DNA technology

A

The transfer of DNA fragments from one organism to another

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13
Q

Why does recombinant technology work

A

Genetic code is universal
Transcription and translation occur by the same mechanism and result in the same amino acid sequence across organisms

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14
Q

Summarise the process of using reverse transcriptase to produce DNA fragments

A

mRNA complementary to the target Gene us used as a template
Mixed with free nucleotides which match up to complementary base pairs and reverse transcriptase which forms sugar-phosphate backbone, to create cDNA

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15
Q

Summarise the process of inserting a DNA fragment into a vector

A

A plasmid used as vector
Cut with same restriction enzyme as DNA so ends are complementary
DNA ligase joins fragment and plasmid together

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16
Q

Summarise the process of using enzymes to produce DNA fragments

A

Restriction endonucleases cut DNA at specific sequences
Different REs cut at different points but one RE will always cut same sequence
So using particular REs allow you to cut out certain Gene of interest

17
Q

Summarise the process of inserting a vector into a host cell

A

Cell transformation
Host cells mixed with vectors in an ice-cold solution + heat to encourage cells to take up the vectors
The cells can then be grown and the DNA fragment cloned

18
Q

Summarise the process of identifying transformed cells

A

Marker genes inserted into vectors along with DNA
When cells grow, UV light can be used to identify which cells have taken up the vector and which haven’t

19
Q

How can DNA probes be used to locate specific alleles

A

Probe designed so that its sequence is complementary to the allele you want to find
They are labelled, amplified using PCR, then added to a sample of single stranded DNA
The probe will bind if the allele is present

20
Q

3 applications of DNA probes

A

Screen someone’s DNA for particular heritable health condition
Identify a gene for use in genetic engineering
To predict how someone will respond to a drug

21
Q

Purpose of DNA hybridisation

A

Measure the degree of difference between 2 DNA stands
Can be used to compare someone’s DNA to a certain gene to see if they have it

22
Q

Summarise the process of DNA hybridisation

A

One DNA stand is labelled and mixed with an unlabelled comparison strand
More similar the strands, the more strongly they will bind
More energy required to break strands apart

23
Q

Benefits of genetic profiling

A

Identifying heritable diseases early
Treatment can be personalised

24
Q

What is genetic fingerprinting

A

Technique used to compare 2 DNA samples + determine weather they came from same individual

25
Q

How does genetic fingerprinting work

A

Every organism’s genome contains non-coding regions called variable number tandem repeats
Probability of 2 individuals having the same VNTRs is very low, so we can compare these areas to see if 2 DNA samples came from same person

26
Q

Summarise the process of genetic fingerprinting analysis

A

DNA sample obtained
VNTRs cut out using restriction enzymes
Labelled + cloned using PCR
Fragments separated using gel electrophoresis
Banding patterns of each sample can be compared

27
Q

How does gel electrophoresis work

A

DNA fragments are placed at one end of a slab of gel
Electrical current applied causing the DNA fragments to move towards the other end of the gel
Shorter fragments travel further
Pattern of bands created unique to every individual

28
Q

Applications of genetic fingerprinting

A

Forensics identify victims or suspects
Medical diagnosis e.g. to identify type of haemoglobin produced by an individual to diagnose sickle cell anaemia
Animal + plant breeding (breed out harmful alleles)