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DNA Science

Molecular biology has progressed at an amazing rate in the last two decades yielding a set of tools that allow us to manipulate DNA in a very controlled way. The aim of this section of the courses is to show a set of examples of the different tools that can be used to solve a wide variety of problems. Our claim is that, at least when dealing with E. coli, it is mostly about asking the right question rather than developing new techniques.

The particular goal of the project is to extract a plasmid from E. coli that contains the beta-galactosidase enzyme, which turns colonies blue in the presence of the sugar X-gal, cut out the beta-galactosidase gene, and replace it with a gene that causes the cells to fluoresce. In order to accomplish this the students have to become acquainted with restricition enzymes, gel electrophoresis, PCR, ligation,and transformations.

Besides the obvious objective of manipulating DNA we had an extra question in mind. As an introduction to measuring gene expression we raised the question: "does the relative change in gene expression depend on the reporter gene that is used?" The relevance of this question is obvious if one is trying to be quantitative... the message should not depend on the messenger! This particular question is one of the advanced projects that is sometimes offered at the end of bootcamp.

Careful planning and understanding of the involved processes and their results is needed. We used Invitrogen's VectorNTI software in an intensive way, which allowed us to graphically understand what would happen to the DNA molecules in each step of this series of experiments. During these types of tutorials all students get to use the software on their computers and plan the next steps for the particular DNA molecule they will do cloning on.

Vector NTI allows to view commented DNA, and its features making it easy to predict restriction fragments, design PCR or sequencing primers and do BLAST searches of particular features of the DNA sequence we might be interested in.

General Concept

We used the pZ system developed by Lutz and Bujard (pZE21, Lutz and Bujard, 1997) as our vector. Its main advantage is that it has unique restriction sites around each one of its important features (coding region, antibiotic resistance, origin of replication, etc.), making it a highly modular plasmid system.

We worked with pZE21-lacZ which expresses beta-galactosidase (the protein coded for by the lacZ gene) under the control of a tetracycline inducible promoter (PLtetO-1). The plasmid also has resistance against the antibiotic kanamycin and its origin of replication is ColE1 (50-70 copies per cell).


Restriction Digest and Gel Electrophoresis

The original vector was digested with the restriction enzymes KpnI and HindIII and the samples were run on an agarose gel. This is a good chance for the students to perform a gel calibration using a DNA ladder.

Two bands are visible in the double digest, one corresponding to the vector (~2300bp) and the other one corresponding to the lacZ gene (~3000bp), which we discard..

Using Qiagen's Gel Extraction Kit we purified the band corresponding to the vector (pZE21), which was going to be ligated with an insert consisting of the gene encoding for one of several fluorescent proteins, Cherry (red), Venus (a yellow fluorescent protein derivative), or Cerulean (cyan fluorescent protein) .


Polymerase Chain Reaction (PCR)

Primers were designed to amplify the lacZ gene from wild type E. coli and to add the correct restriction sites on either side. In order to illustrate the amplification process we measured the quantity of PCR product as a function of time using two methods. First, the hard way, by stopping the PCR reaction each cycle and extracting small aliquotes which can then be run on a gel; second, the easy way, by doing a qPCR assay which gives a fluorescent signal proportional to the amount of DNA in the reaction at each time point.

Ligation and Transformation

The vector and the insert were ligated together using T4 Ligase. The product was transformed into DH5a cells, which lack the tetracycline repressor (TetR). The absence of this repressor means that, in the case of a successful ligation, the cells will express the fluorescent protein ligated into the plasmid at a high level. It was then easy to screen for these colonies by plating them on agar with both X-gal and kanamycin. The presence of kanamycin ensures that only cells that took up a plasmid will grow (DH5a cells do not contain a kanamycin resistance gene); the presence of X-gal ensures that colonies that took up any original plasmid still present in the ligation mix will be blue and therefore readily identifiable. Cells which took up the desired plasmid with a fluorescent protein gene will glow under the appropriate illumination.


Lutz R and Bujard H, Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I1-I2 regulatory elements, Nucleic Acids Research, 1997; 25(6):1203-10.


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