19. Genetic Technology Notes Flashcards
Recombinant DNA
DNA that contains genetic material from 2 different organisms
Main stages used in gel electrophoresis to separate and locate DNA fragments cut with restriction endonuclease
(Paper 5)
- Amplify DNA by PCR (should be done before cutting)
- Make agarose gel & Add buffer solution
- Add loading dye to each sample
- Load samples into wells at negative end (cathode) of gel
- Apply current between electrodes
- Stain DNA using ETHIDIUM BROMIDE {fluoresces} & observe DNA under UV light
- Hazard and safety precaution:
- do not touch connectors with wet hands, to prevent electrocution
- wear safety gloves b/c ethidium bromide is harmful
* EtBr will bind to DNA, mutagen and carcinogenic
How is gel electrophoresis used to distinguish between two alleles of a gene?
- DNA is cut with restriction enzymes
- Agarose gel is immersed in a buffer solution
- DNA fragments are loaded into wells in the gel, at cathode
- Current is applied, creating an electric field
- Fragments are negatively charged, so they move towards the ANODE
- Gel acts as a molecular sieve
- Smaller fragments move faster and further than larger ones
- Current is switched off
- Carry out Southern blotting, by transferring fragments to a membrane {used to identify specific fragments}
- Add radioactive probes for visualisation under X-ray / fluorescent dye under UV light
* probes will hybridise to complementary DNA bases - Compare banding patterns; the alleles have different positions on gel
Variations to gel electrophoresis for separating polypeptides
- Gel is stained using Coomassie blue stain to be visible, as polypeptides are colourless
- Western blotting
- Identify specific polypeptides by using (monoclonal) antibodies tagged with fluorescent dye
- We can differentiate 2 different polypeptides with a similar size by comparing their net charges
How is microarray analysis done?
- mRNA extracted from 2 samples (interest + control)
- REVERSE TRANSCRIPTASE is used to produce cDNA from mRNA
- cDNA amplified by PCR
- DNA labelled with DIFFerent colour fluorescent dyes
- Labelled DNA is denatured to produce ssDNA
- Microarray chip has ssDNA PROBES - each probe is from a known gene
- DNA hybridises to probes on microarray chip
- Excess (unbound) cDNA is washed away after hybridisation - Microarray chip is scanned with UV light to record fluorescence pattern; fluorescence shows the expressed genes
- Intensity of fluorescence shows level of gene expression - Compare fluorescence between the 2 samples
Bioinformatics
Database collection for the analysis of biological information and data using computer software
❖ Outline how sequencing the genome of Plasmodium and the use of bioinformatics can suggest new targets for anti-malarial drugs. [3m]
- identify genes
- predict primary structure of proteins
- predict (& model) 3D/tertiary structure of proteins
- identify function of protein from 3D structure
- develop drugs that bind with protein to block activity of protein
- develop drugs that prevent transcription of genes
Explain how DNA sequencing could be used to compare the DNA of 2 species. [4m]
- DNA cut into fragments by restriction enzymes
- DNA denatured to produce ssDNA
- primers added for annealing, attach to start of DNA
- dideoxyribonucleotide chain termination is carried out
- using DNA polymerase & copies of different lengths are produced
- then, gel electrophoresis is carried out
- laser scanner is used to detect fluorescence
- sequence of bases read by computer
5 advantages of producing human proteins by recombinant DNA techniques
eg.
- insulin
- factor VIII for the treatment of haemophilia
- ADENOSINE DEAMINASE (ADA) enzyme for treating severe combined immunodeficiency (SCID)
- Unlimited supply
- Less risk of transmitting disease
- Cost of purification is lower
- Lower risk of allergy/side effects
- Potential to improve recombinant protein
8 advantages of screening for genetic conditions
eg.
- genes for breast cancer, BRCA1 and BRCA2
- genes for haemophilia, sickle cell anaemia, Huntington’s disease and cystic fibrosis
- Provide information about the increased risk of person having genetic conditions
eg. breast cancer - Can prepare for late onset genetic conditions
eg. Huntington’s disease - Identify whether foetuses are going to develop a genetic condition…
- so can give early treatment when born
- Allows parents to prepare for the birth of a child who will need treatment {eg. financially}
- Identify carriers of genetic conditions
- Help to provide early diagnosis
- Allow couples who are both carriers of a genetic condition to make family planning decisions (can choose IVF)
Discuss the social and ethical considerations of using gene testing (embryos for genetic diseases) and gene therapy in medicine
3 pros & 4 cons
Pros
+ can avoid having offspring with serious genetic disease
+ can avoid late abortions (if genetic disease discovered later in foetal development)
+ allow couples to have children who would otherwise choose not to due to risk of genetic disease
Cons
- viable embryos discarded
- may conflict with religious beliefs
- could lead to selection based on gender or specific traits (“designer babies”)
- ? may be waste of healthcare resources to test for genetic conditions that have no treatment available, eg. Huntington’s disease
4 aims of gene therapy
What type of genetic disease is suitable for treatment with gene therapy and why?
- insert a normal ALLELE to obtain normal protein
- reduce symptoms of the disorder
- restore cellular functions
eg. enzyme reaction, blood clotting protein, membrane transport - improve quality of life / life expectancy
Genetic disease in which faulty allele is RECESSIVE.
- only 1 copy of normal, dominant allele needs to be inserted per cell
- to synthesise correct protein
- to cure disease
- no need to remove faulty allele, as would be the case if faulty allele was dominant
7 symptoms of cystic fibrosis (CF)
- thick, sticky mucus
- build up in lungs
- lung infections, which damage lungs
- mucus blocks pancreatic duct and prevents secretion of digestive enzymes from pancreas,
- causing malnutrition, due to inadequate digestion and absorption
- reduced growth
- mucus blocks sperm duct, sterile males
How can cystic fibrosis be treated with gene therapy?
- an autosomal recessive disease
- CF is caused by MUTATION of CFTR gene, making the CFTR gene defective & faulty CFTR protein is produced
- so insert normal dominant CFTR allele into DNA…
- …in cells of respiratory system
- by using a VECTOR
- use liposomes, which are sprayed and inhaled
- use harmless virus - ADENOVIRUS
- correct form of CFTR protein made
- inserted into membrane
- act as CHLORIDE CHANNEL to actively transport chloride ions out of cell
- water potential decreases outside cell, so WATER leaves cell by osmosis
- normal mucus formed
- symptoms reversed
eg. less chance of lung infections
Outline how genetic diseases can be treated with gene therapy
- obtain normal allele from healthy person {cut using restriction enzymes, sticky ends}
- insert into vector
- use liposomes as vector
- liposomes are sprayed as an aerosol and inhaled {suitable for respiratory diseases}
- liposomes fuse with host cell - use harmless virus as vector
- may cause side effects - effects are short-lived & repeat treatments are needed