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Gene Technology Chapters 11 & 13. Gene Expression 0 Genome 0 Our complete genetic information 0 Gene expression 0 Turning parts of a chromosome “on” and.

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Presentation on theme: "Gene Technology Chapters 11 & 13. Gene Expression 0 Genome 0 Our complete genetic information 0 Gene expression 0 Turning parts of a chromosome “on” and."— Presentation transcript:

1 Gene Technology Chapters 11 & 13

2 Gene Expression 0 Genome 0 Our complete genetic information 0 Gene expression 0 Turning parts of a chromosome “on” and “off”

3 Gene Expression 0 Uncoiled chromosomes are called euchromatin 0 We have two parts to our genes 0 1. Introns 0 Transcribed but not translated 0 Cut out of mRNA before leaving nucleus 0 2. Exons 0 Transcribed and translated 0 Codes for a protein http://highered.mcgraw-hill.com/olcweb/cgi/pluginpop.cgi?it=swf::535::535::/sites/dl/free/0072437316/120080/bio31.swf

4 Transcription 0 DNA  mRNA 0 After mRNA has been made in the nucleus 0 Introns are spliced out of the mRNA 0 Exons bind together 0 Addition of 5’ cap and poly A tail

5 Gene Regulation 0 Similar to bacteria except out genome is much larger and more complex 0 98% of our DNA does not code for a protein 0 Each person has a specific number of non-coding regions between exons 0 Called VNTR (Variable Number Tandem Repeats) 0 Nonsense repeats in tandem

6 DNA Identification 0 Used to identify criminals in a crime scene or to see family relation 0 Four steps to use DNA identification 0 1. Isolate DNA (make copies if small sample) 0 2. Cut DNA in fragments that are known VNTR areas 0 3. Sort DNA by size (using technology) 0 4. Compare size fragments to known samples http://www.youtube.com/watch?v=ZxWXCT9wVoI

7 How to Make DNA Copies 0 Process called PCR 0 Technology where a small DNA sample can be amplified to many copies for analysis

8 PCR Steps 0 1. Add sample of DNA, DNA polymerase enzyme, free nucleotides (to make new strands with) and heat sample 0 The heat will act like helicase and separate the strands of DNA

9 PCR Steps 0 2. Cool sample down so primers can be added to DNA template strands

10 PCR Steps 0 3. DNA polymerase attaches to primers and adds nucleotides to rest of DNA template strands

11 PCR Steps 0 4. Two new strands are made  repeat process until enough DNA sample http://www.youtube.com/watch?v=2KoLnIwoZKUhttp://www.youtube.com/watch?v=eEcy9k_KsDI

12 Cutting DNA 0 Technology that cuts long strands of DNA 0 Biologists use restriction enzymes in order to cut the DNA 0 Biological scissors 0 Restriction enzymes can recognize specific sequences and only cut in certain areas of DNA

13 Cutting DNA 0 Sometimes when restriction enzymes cut DNA they leave an overhang 0 Creates “sticky” ends where you can then add recombinant DNA 0 Used to input DNA from other organisms into a genome http://highered.mcgraw- hill.com/olcweb/cgi/pluginpop.cgi?it=swf::535::535::/sites/dl/free/0072437316/120078/bio37.swf

14 Gel Electrophoresis 0 Technology that separates DNA fragments by size in a gel to compare to known samples

15 Gel Electrophoresis 0 How to run a gel: 0 1. DNA sample goes through restriction enzymes to break into fragments of known VNTRs 0 2. Each DNA sample (now cut up) gets added into its own chamber well

16 Gel Electrophoresis 0 3. Electric current is run through the gel for a specific amount of time 0 DNA is negatively charged 0 End of gel is positively charged 0 When current runs, the DNA fragments move towards the end of the gel

17 Gel Electrophoresis 0 4. DNA is transferred to a nylon membrane where probes are added 0 Probes bind to complementary DNA

18 Gel Electrophoresis 0 5. X-ray film exposes membrane 0 This creates a band pattern that is unique to each individual 0 Called a “bio fingerprint” 0 You can create a permanent copy of results if needed to file

19 Gel Electrophoresis 0 How to read results: http://learn.genetics.utah.edu/content/labs/gel/

20 Recombinant DNA 0 Genetic engineering: modifying a genome of living cell 0 When you combine two DNA strands from different organisms it is then called recombinant DNA

21 Cloning 0 Clone 0 Exact copy of DNA, a cell or an organism 0 Clones can be created by inserting DNA into vectors 0 Vectors are organisms that can replicate itself 0 Ex: bacteria, yeasts

22 Cloning 0 1. Egg cells are extracted from one organism and the nucleus is removed 0 Nucleus removed because the DNA of the organism we want needs to fuse into the egg 0 Cells from organism we wish to clone are removed

23 Cloning 0 2. Desired organisms cell is placed next to egg cell and electric shock fuses the two cells into one 0 This triggers the new embryo to begin to divide and develop

24 Cloning 0 3. Developing embryo is implanted in a surrogate mother and after incubation period is over, a new baby organism is born with the exact same genetic information as original organism http://www.youtube.com/watch?v=tELZEPcgKkE http://www.youtube.com/watch?v=-Qry1gYYDCA

25 Vaccines 0 Substance containing all or part of a harmless strain of a pathogen 0 This gets introduced to our body and we build an immunity for it creating a defense system against the pathogen called antibodies 0 DNA vaccine: vaccine containing genes from pathogen but will not cause infection http://highered.mcgraw-hill.com/olcweb/cgi/pluginpop.cgi?it=swf::535::535::/sites/dl/free/0072437316/120078/bio39.swf http://www.youtube.com/watch?v=SduMbjW2V9A

26 Agricultural Applications 0 Made plants more tolerable to our environment 0 Resistance to weeds 0 Added genes that would be harmful to insects and pests 0 Increase nutritional value to some plants 0 Ex: adding vitamin A to rice in Asia http://www.youtube.com/watch?v=FTfuAbzAeB8http://www.youtube.com/watch?v=FTfuAbzAeB8 – food http://www.youtube.com/watch?v=JVIznPgdQSM – animalshttp://www.youtube.com/watch?v=JVIznPgdQSM


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