Genetics Flashcards
1
Q
Outline the steps of Gene Transfer
A
- identify gene of interest within the DNA
- identify vector, the plasmid of prokaryotic DNA
- Use restriction enzymes to extract gene from DNA and cut space for DNA to go into the plasmid. The enzyme will create sticky ends within the DNA and vector, ensuring easy insertion.
- Employ ligase enzyme to join vector and gene together and fuse complimentary sticky ends together.
- Introduce recombinant construct into host cell. Now it can produce designated substance.
- many times used to produce proteins, such as insulin
2
Q
Outline the steps for Gel Electrophoresis
A
- used to separate DNA based on mass/size/ charge
1. restriction enzymes used to chop DNA into fragments
2. fragments placed in wells on one side of gel substance
3. electrical current passed through gel
4. fragments light in mass and charged will move faster towards the positive charge
3
Q
Where does genetic variation come from?
A
- random/ independent assortment during Metaphase I and II of Meiosis
- random fertilization
- crossing over during prophase I of meiosis
4
Q
What is the human genome project used for?
A
- compare genetic makeup of populations
- track ancestry
- track migrations of populations
5
Q
Describe base substitution of sickle cell anaemia
A
- substitution of valine for glutamic acid in hemoglobin bases
- causes sickle shape of red blood cell instead of biconcave
- affects ability of red blood cells to carry oxygen
- substitution also causes haemoglobin to crystallize inside of red blood cell, leading red blood cells to become less flexible so they get stuck in capillaries
- resistant to Malaria, a beneficial adaptation in Africa
6
Q
Outline steps of Karyogram
A
- stain cell and place under light microscope
- take picture of condensed chromosomes during Metaphase
- cut out chromosomes from pictures
- sort them according to size, banding pattern, shape into homologous chromosomes
7
Q
Outline steps of Autoradiography
A
- used as a way to get images of DNA so their lengths can be measured
1. DNA is inserted with radioactive form of thymidine
2. DNA left in dark for a period of time
3. DNA placed under electron microscope
4. black dots appearing on DNA represent the radioactively decaying atoms
8
Q
Different ways to acquire cells for karyotyping
A
- Extract cells from amniotic fluid
- using hypodermic needle - Extract cells from villus tissue of placenta
9
Q
Outline Plant cloning
A
- vegetative propagation- small pieces can grow independently
- due to meristematic tissue- totipotent stem cells
- occurs in garlic and onion bulbs, and strawberry runners
- produce genetically identical plants
10
Q
Outline the different methods of Animal Cloning
A
BLACK BEARS FART POOP
- Binary Fission- parent organism divides into 2 genetically identical daughter organisms. Eg bacteria
- Budding- cells split off from parent organism, forming daughter organism. Ex yeast
- Fragmentation- new organisms grow from fragments of parent organism. Starfish
- Parthenogenesis- organisms grow from unfertilized ovum. ex frogs
11
Q
Outline the 2 different methods of Human Cloning
A
- monozygotic- 2 identical twins are produced from a fertilized zygote splitting into 2 cells
- dizygotic- 2 non-identical twins are produced from unfertilized egg splitting into 2 cells, and fertilized from 2 different sperm cells
12
Q
Outline steps of PCR (Polymerase Chain Reaction)
A
- add nucleotides and DNA
- Heat to 90 degrees Celsius. The heat acts as Helicase, breaking Hydrogen bonds in DNA and exposing bases
- Low temperature to 55 degrees Celsius, and primers anneal.
- Heat to 75 degrees Celsius, the optimum temperature for the thermostable polymerase III. This enzyme speeds up the annealing of primers