Unit 8 - The control of gene expression Flashcards

1
Q

Types of mutations

A

Substitution
Deletion
Addition
Duplication
Inversion
Translocation

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2
Q

Why don’t all mutations affect the order of amino acids

A

Because Dna is degenerate

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3
Q

Why do additions, duplications and deletions have a higher chance of causing mutation?

A

They cause a frame shift which affects more codons

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4
Q

3 ways that mutagenic agents can cause mutation

A

Act as a base
Alter bases
Changing structure of DNA

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5
Q

Features of benign tumours

A

Non cancerous
Slow growing
Cannot form metastases

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6
Q

Features of malignant tumours

A

Grow rapidly
Form metastases
Travel using blood/ lymphatic system

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7
Q

Features of tumour cells

A

Irregular in shape
Larger nucleus
Don’t produce full proteome
Dont respond to growth- regulating processes
Divide more frequently than other cells

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8
Q

Features of tumour cells

A

Irregular in shape
Larger nucleus
Don’t produce full proteome
Dont respond to growth- regulating processes
Divide more frequently than other cells

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9
Q

Two types of factors that increase risk of cancer

A

Environmental factors
Genetic factors

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10
Q

Two types of factors that increase risk of cancer

A

Environmental factors
Genetic factors

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11
Q

What are stem cells

A

An unspecialised cell which can multiply indefinitely and can differentiate to become a specialised cell

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12
Q

4 types of stem cells

A

Totipotent
Pluripotent
Multipotent
Unipotent

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13
Q

What can stem cells be used to treat?

A

Spinal cord injuries
Heart disease and damage
Bladder conditions
Respiratory diseases
Organ transplants

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14
Q

3 sources of stem cells

A

Adult stem cells (Bone marrow)
Embryonic stem cells (Embryos 4-5 days old)
Induced pluripotent (Specialised cells which have been treated)

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15
Q

Ethical issues with embryonic stem cells

A

It is destruction of an embryo which could become a fetus
At the moment of fertilisation the induvidual has the right to life
Adult stem cells ar not as useful as embryonic stem cells
Some induced pluripotent stem cells may be rejected by the body

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16
Q

Steps for oestrogen promoting transcription of genes

A
  • Oestrogen binds to a transcription factor forming an oestrogen- oestrogen receptor complex
  • This activates the transcription factor
  • This then binds to the promoter region of the gene
  • This allows RNA polymarase to bind and transcription to occur
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17
Q

Types of interfering molecules

A

SiRNA
miRNA

18
Q

Which is more complementary to the DNA- miRNA or siRNA

19
Q

How does siRNA work

A

Associates with proteins which cut the DNA when siRNA binds

20
Q

How does miRNA work?

A

Associates with proteins which block transcription when miRNA binds

21
Q

How does methlation affect transcription?

A

Decreases transcription of gene

22
Q

How dooes acetylation offect transcription?

A

Increases transcription of gene.

23
Q

Why is ot harder to translate the genome of complex organisms?

A
  • They have large sections of non- coding DNA
  • ## They have large complex regultory genes
24
Q

Why use newer sequencing methods?

A
  • Less labour intensive
  • Cheaper
  • Can be done on a much larger scale
25
methods of isolating genes
Using reverse transcriptase to produce CDNA Using restriction endonuclease enzymes Gene machine
26
Methods of gene amplification
In vivo- gene inserted into a vector- vector inserted into host cell In vitro- using PCR
27
Methods of identification of transgenic host cells
Marker genes
28
Types of gene mutations
Addition Deletion Substitution Inversion Duplication Translocation
29
Step 3- Identification of transformed organisms
- Marker genes inserted at same time as gene being replicated - Host cells grown on agar plates - Marker gene can code for antibiotic resistance - Colonies which survive in antibiotic are grown (replica plating)
30
Two types of gene therapy
Somatic therapy- Body cells Germ line therapy- Sex cells
31
Uses of screening using DNA probes and hybridisation
Identifies heritable conditions Determines how a patient will respond to specific drugs To identify health risks
32
Using electrophoresis to compare DNA of samples
- DNA cut - Using restriction endonuclease - Use electrophoresis - Separate according to length - Add absorbent paper to make them visible (southern blotting) - Make single-stranded by heating/ using alkali - Apply radioactive probe and use autoradiography - Different tandem repeats= different length
33
Uses of genetic fingerprinting
- Determine genetic relationships - Determine genetic variability within a population - Determine culprit in forensic science - Medical diagnosis - Animal and plant breeding
34
Uses of human genome project
- Aids the understanding of gene function and interaction - Scientists can identify genes which are linked to cancer - Identified genes related to Alzheimers
35
Medical uses of Identifying genes
Identifying dangerous alleles which have been inherited
36
General uses of identifying genes
Checking parents of child Selective breeding Forensic science in crime
37
Application of genome projects
Genetic screening for inherited diseases Developing medical treatments for genetic diseases
38
What are primers and what do they do?
Single-stranded DNA Mark beginning and end of DNA being amplified
39
What is a vector
Carrier of DNA/ gene into another cell
40
Steps in PCR
Temperature is increased to 95 degrees to split DNA into single strands Temperature then cooled to 55 degrees to allow primers to anneal Heated again to 72 degrees which is optimum temperature for DNA polymerase to replicate DNA
41
In what direction do strands move in electrophoresis
From negative to positive electrode
42
What can DNA hybridisation be used for
Screen for heritable conditions Check potential drug responses Check for health risks