20.109(F12):Module 1
Module 1
Instructors: Bevin Engelward, Shannon Hughes-Alford, Natalie Kuldell, Agi Stachowiak
TA: Jenny Kay (Engelward Lab) 
In this experimental module you will modify the gene for EGFP (Enhanced Green Fluorescent Protein) to truncate the protein it encodes. Cells expressing the full-length protein glow green when exposed to light of the appropriate wavelength. You will be designing and then creating an expression vector to delete the first 32 amino acids of EGFP. Cells transfected with your expression vector should not glow green, a prediction you will test. You will also test whether this N-terminally truncated EGFP can recombine with a C-terminally truncated version to regenerate full length EGFP in vivo. Finally, you will have the opportunity to suggest changes to the experimental protocol that will increase the frequency of green cells in which there has been an inter-plasmid recombination event. We will then choose a few variables to test on the final day of the experiment.


Lablinks: day by day
 Day 1: DNA engineering using PCR
 Day 2: Clean and cut DNA
 Day 3: Agarose gel electrophoresis
 Day 4: DNA ligation and bacterial transformation
 Day 5: Examine candidate clones & introduction to tissue culture
 Day 6: Lipofection & lab certification
 Day 7: FACS analysis
Assignments
 summary of Module 1 assignments
 DNA engineering lab certifications
 Online cloning lab and defense
 FACS data analysis and defense
 DNA engineering powerpoint summary and notes
 blog assignment
References
- DNA double-strand break repair: From mechanistic understanding to cancer treatment
 DNA Repair 2007
 Thomas Helleday, Justin Lo, Dik C. van Gent, Bevin P. Engelward
 URL
 Sample Animation Animations were made by Justin Lo (BE class of '08), a former UROP student in Professor Engelward's laboratory!
- Homologous recombination as a mechanism of carcinogenesis
 Biochim Biophys Acta 21 March 2001
 Bishop AJ and Schiestl RH
 URL
- Rad51-deficient vertebrate cells accumulate chromosomal breaks prior to cell death
 EMBO J 15 January 1998
 E Sonoda, M S Sasaki, J M Buerstedde, O Bezzubova, A Shinohara, H Ogawa, M Takata, Y Yamaguchi-Iwai, and S Takeda M
 URL
