BISC 219/2009:Creating a Transgenic Organism: Difference between revisions

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[[BISC 219/2009: Mod 3 Structural Evidence for Transgenic Plants| Structural Evidence for Transgenic Plants]]<br>
<font color=green>[[BISC 219/2009: Mod 3 Structural Evidence for Transgenic Plants| Structural Evidence for Transgenic Plants]]</font color=green><br>
Histochemical GUS enzyme activity assay<br>[[BISC 219/2009: Mod 3 GUS Activity Assay by Histochemistry| GUS Activity Assay by Histochemistry]]<br>
Histochemical GUS enzyme activity assay<br><font color=green>[[BISC 219/2009: Mod 3 GUS Activity Assay by Histochemistry| GUS Activity Assay by Histochemistry]]</font color=green><br>
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Revision as of 10:57, 4 September 2009

Wellesley College BISC 219 Genetics

At the end of this semester long series you will have mastered the following skills and concepts using both microorganisms and a multicellular organism.

Schedule of Experiments

Lab # Dates Activity
1 9/8 - 9/14 set-up of plant transformation
Independently 9/11 - 9/17 transfer of explants to selective medium; induce shoots
4 9/29 - 10/5 transfer shoots to root inducing medium
7 10/26 - 10/30 transfer plantlets to soil
8 11/4 - 11/10 single leaf-disc PCR

Structural Evidence for Transgenic Plants
Histochemical GUS enzyme activity assay
GUS Activity Assay by Histochemistry

9 11/11 - 11/17 Restriction enzyme digest of PCR reactions

Agarose gel electrophoresis of digested PCR

10 11/18 - 11/24 Spectrophotometric GUS enzyme activity assay

Phenotypic analysis of plants

11 11/30 - 12/4 Data Analysis Workshop
Dec 11 12/11 Plant Genetic Engineering Paper Due
for all students

Experimental Objectives:

In this semester long experiment you will:

  1. Master aspectic technique and tissue culture;
  2. Use the Agrobacterium system to introduce a foreign gene, the β -glucuronidase gene (gusA) of E. coli, into the cells of tobacco;
  3. Take advantage of the totipotency of plant cells and use these transformed cells to regenerate genetically engineered plants;
  4. Confirm that the regenerated plants are transformed by
    1. measuring the activity of the introduced enzyme, β–glucuronidase (GUS) spectrophotometrically and histochemically;
    2. using PCR to test directly for the presence of the introduced genes.


Concepts Genes/Organisms Techniques/Skills
Effect of random gene insertion in a large genome Vector bacterium: Agrobacterium tumefaciens Aseptic tissue culture
Plant totipotency Transgenic recipient: Tobacco plant- Nicotiana tobacum DNA Extraction
Regulation of gene expression Transgene: gusA gene from Escherichia coli encoding beta-glucoronidase PCR
Genetic Engineering and creation of genetically modified organism Agarose gel electrophoresis
Phenotypic Selection Transfection & selection by antibiotic resistance;

Enzyme function assays: colorimetric & histochemical


Background
Transgenic Plants: Media Recipes
Lab 1: Creating the Transgenic Plant: Day 1
Outside of Lab in the first week: Creating the Transgenic Plant: Days 3-5
In Lab 4: Creating the Transgenic Plant: Week 4-5
In Lab 7-8: Creating the Transgenic Plant: Week 8
Lab 8: Assaying the Transgenic Plants: DNA extraction, PCR, GUS by histochemistry
Lab 9: RE digestion, Agarose gel electrophoresis of the PCR product
Lab 10: Spectrophotometric GUS activity assay
Lab 11: Analyzing the data on the putative transgenic and control plants