Genetic Modification 3.5.

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Presentation transcript:

Genetic Modification 3.5

PCR Polymerase chain reaction (PCR) is an artificial method of replicating DNA Used to amplify large quantities of a specific sequence of DNA from a small sample Why would you want to do this? Each reaction cycle doubles the amount of DNA

PCR A thermal cycler is used to complete the PCR process Denaturation Annealing  Elongation 

Restriction Endonucleases Aka restriction enzymes Cut DNA at specific locations known as restriction sites Each enzyme cuts at a different site Can produce blunt ends or sticky ends

Restriction Mapping How many pieces would you have if you were to cut the plasmid with ScaI? What would their sizes be? What about NzuI?

Genetic Modification Gene modification is carried out by gene transfer between species The genetic code is universal so an organism can potentially express a new trait if the appropriate gene is introduced into its genome The transfer of genes between species is called gene modification, and the new organism created is called a transgenic

Genetic Modification Four main steps: Isolation of gene and vector (by PCR) Digestion of gene and vector (by restriction endonuclease) Ligation of gene and vector (by DNA ligase) Selection and expression of transgenic construct

Isolation of gene and vector Isolate DNA Use PCR to amplify A vector is chosen

Digestion with restriction enzymes In order to incorporate a gene of interest into a vector, both must be cut with restriction enzymes at specific recognition sites

Ligation of vector and insert The gene and vector are then spliced together by the enzyme DNA ligase to form a recombinant construct

Selection and expression The recombinant construct is introduced into an appropriate host cell or organism Antibiotic selection is commonly used in order to identify which cells have successfully incorporated the recombinant construct Transgenic cells, once isolated and purified, will hopefully begin expressing the desired trait encoded by the gene of interest

Gel Electrophoresis Gel electrophoresis is used to separate proteins or fragments of DNA according to size Create a DNA fingerprint

Gel Electrophoresis DNA may be cut into fragments using restriction endonuclease DNA samples are placed into an agarose gel Electric current is run through the gel causing the negative DNA to move to the positive end

Gel Electrophoresis

Gel Electrophoresis

Gel Electrophoresis Proteins may also be used in this process Proteins may be folded into a variety of shapes (affecting size) and have positive and negative regions (no clear charge) Protein samples are placed into a polyacrylamide gel Electric current is run through the gel separating the protein fragments

Cloning Clones are groups of genetically identical organisms, derived from a single original parent cell

Cloning Natural Cloning All bacteria, the majority of fungi and many species of protists reproduce asexually to produce genetic clones Binary Fission Budding Fragmentation

Cloning

Cloning Plants have the capacity for vegetative propagation, whereby small pieces can be induced to grow independently

Cloning Even human beings are capable of creating genetic clones through natural means

Cloning Artificial cloning At a very early stage, embryonic cells retain pluripotency Separated artificially and then implanted into a surrogate This method of cloning is limited by the fact that the embryo used is still formed randomly via sexual reproduction and so the specific genetic features of the resulting clones have yet to be determined

Cloning Second method of artificial cloning is SCNT Stem cells can be artificially generated from adult tissue using a process called somatic cell nuclear transfer (SCNT) Steps in virtual lab

Cloning Two different types of cloning with different purposes Reproductive cloning: Therapeutic cloning: 

GMOs Genetically modified organisms (GMOs) are used in agriculture to improve crop yields and reduce farming costs However the use of GM crops is a contentious issue, as economic benefits must be weighed against environmental risks

GMOs Human health Can incorporate genes for certain proteins, vitamins, or vaccines Can be made to lack common natural allergens or toxins Could trigger unexpected adverse health reactions in some individuals Currently, not all foods with GM components are labelled, making informed decisions of use difficult for consumers

GMOs Economics Grow in a wider range of environments (e.g. drought / frost / salinity resistance) Produce greater yields (crops can potentially grow larger and faster) Slow the rate of spoiling, leading to longer shelf lives for GM foods Resistance to certain viruses or produce toxins to pests Herbicide resistant crops can be used to allow for the easier killing of weeds (which compete with crops for soil nutrients) Improved yield, reduction in farming costs and ability to farm more land will provide an economic benefit to farmers Patent protection allows biotech companies to restrict the use of seeds and force farmers to pay high prices for use

GMOs Environment The ability to farm a wider range of environments with GM crops will potentially reduce the need for associated deforestation Generation of pest-resistant crops means that less chemical insecticides will be released into the environment GM crops could potentially reduce biodiversity in a region by competing with indigenous plant life Furthermore, proteins or toxins produced by GM crops could negatively affect certain organisms within the ecosystem Cross-pollination by GM crops could also result in the formation of herbicide- resistant weeds and grasses GM crops with pest toxins could also accelerate the evolution of resistant pest species

GMOs Analysis of data on risks to monarch butterflies of Bt crops On edmodo