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Selective Breeding + Gene Cloning may change the genetic nature of a species
SELECTIVE BREEDING
Breeding of organisms according to selected desirable characteristics
HISTORY OF SELECTIVE BREEDING OF ONE SPECIES FOR AGRICULTURAL PURPOSES SERIES OF CHANGES OCCURRED IN SPECIES AS A RESULT Canola Breeding in Australia
1969: First commercial crop -high levels erucic acid + glucosinolates - susceptible to blackleg disease = problems many losses 1970s: Breeding program improved varieties; Wesreo + Wesway + Lower erucic acid + greater blackleg resistance 1980: Marnoo + Lower glucocinolate + higher yielding - limited blackleg resistance -> growers preferred Jumbuck * 1987: Maluka + Shiralee + improved yields + disease resistance + lower erucic acid + glucosinolates 1993: Herbicide Triazine resistance = compete with weeds (kill weeds w/o affecting crops) Ability to mature earlier/later in year = more widespread cultivation across country
GENE CLONING
Creation of a genetically identical copy of a certain gene Involves: selected gene -> spliced + inserted into another org -> copies of gene DNA recombinant technology (recombining DNA to clone genes) - Can be used to produce a certain protein Eg. Insulin needed by diabetics by cloning the human gene for insulin -> restriction enzymes (splice) cut out/isolate insulin gene from DNA + cut through plasmid DNA -> insulin gene + plasmid = attach = recombinant plasmid formed -> insert -> bacteria which reproduces asexually = all contain copies of insulin gene Bacteria serve as biological factories producing human insulin = source for diabetics 1. Restriction enzymes splice human insulin gene -> plasmid = recombinant plasmid 2. Insert -> bacteria -> reproduce asexually = identical copies of bacteria all contain copes of insulin gene 3. Serve as bio factories producing human insulin = reliable source for diabetics
PRODUCTS
METHODOLOGY
GENE CLONING Transfer copies of genes from one organism to another intro new gene into species PART OF DNA extracted -> ANOTHER SPECIES Identical copies of GENE ONLY (bacterium genetic makeup changed)
WHOLE ORGANISM CLONING Reproduce genetically identical populations ALL DNA extracted -> egg cell SAME SPECIES Identical DNA + GENETIC MAKEUP to organism cloned
PROCCESSES USED IN CLONING OF AN ANIMAL + WAYS IN WHICH SCIENTISTS COULD VERIFY THAT THE ANIMAL PRODUCED WAS A CLONE
Cloning methods: Nuclear Transfer - unfertilized egg -> enucleated to remove nucleus - DNA of desired organism inserted/fused -> egg fertilized - allowed to reproduce (multiply) -> embryo implanted into uterus
Methods to Identify the Organism is a Clone: Nuclear Transfer: involves replicating the organisms WHOLE DNA (diploid cell -> unfertillised enucleated egg) = resulting cloned organism should have identical DNA with that of original parent Thus clones can be verified by DNA Hybridisation: DNA from both organisms is extracted Heat -> hydrogen bonds break -> DNA separates -> single strands. Single strands mixed together -> since the organisms are clones (genetically identical) = single strands should match up completely (no non-complementary sections)