In biology, we study living organisms, and the key to understanding a living organism, is to understand the expression of its genome. What genes are present in the genome, and what proteins are produced when these genes are expressed? Beyond this, we may want to understand what is going on in a particular cell within an organism. How does a particular cell type perform gene expression? How has gene expression been altered in a cancer cell?
A common approach for answering these questions involves identifying the mRNAs being made by a particular cell during transcription. From this information, a number of techniques can be performed,
Alysing gene expression will typically involve isolating mRNAs from a cell, because from these we can perform the reverse transcriptase-polymerase chain reaction, or RT-PCR. This is where we take an mRNA and create a complementary DNA strand, in essence reverse engineering the DNA template that would have generated the mRNA during transcription. That is why the enzyme that performs this function is called reverse transcriptase, as the process is essentially the reverse of transcription.
Whenever we do this, reverse transcriptase will use the mRNA as a template to generate a single-stranded DNA molecule that is the complement of the mRNA. mRNAs have a poly-A tail, or a number of adenine RNA bases in a row, so we can use a poly-dT primer, or a series of thymine DNA bases, to help reverse transcriptase get going.
Once completed, another enzyme is used to degrade the mRNA, and then DNA polymerase is used to synthesize the complementary DNA Strand, resulting in double-stranded DNA, which we will call complementary DNA, or cDNA.
Applications of RT-PCR
When a gene is being expressed during the embryonic development of an organism. We could isolate the mRNAs from different stages of development, and perform RT-PCR to get cDNA fragments that correspond to all of these mRNAs. Then we could amplify a specific cDNA molecule that represents the gene of interest, using the polymerase chain reaction, by employing a primer that is specific to the gene of interest, so that only the cDNA representing the gene of interest is amplified.
We can repeat this process for each of the stages of embryonic development we are testing. Then we can perform gel electrophoresis, witha column for each stage of development, whereby only the amplified product will be relevant, since it will be so much more abundant than anything else. If we get a lot of the gene of interest, it means that the mRNA it produces was present in the sample during that stage, because its presence was necessary in order to get the corresponding cDNA in the first place.
So this is how we can tell when a particular gene is being expressed in the embryo. Quite similarly, this approach can be used to determine which tissues within an organism are expressing a particular gene, by extracting mRNA from different tissues, and going through the same process with cDNA and amplification to see which tissue samples contained the mRNA associated with the gene of interest.
DNA Microarray
Biologists are often interested in understanding genome-wide expression. In other words, we want to understand the ways that many different genes act together to produce and maintain a functioning organism. To do this, we will typically perform something called a DNA microarray assay. This is a powerful technique involving a huge grid of tiny spots, and in each well sits many copies of a single-stranded DNA fragment called a probe, attached to a solid surface, which each represent a particular gene.
So we can think of this as a grid of many different genes of an organism, or even all of them, ideally. Then, by the process we already discussed, mRNAs that are made in a cell of interest are isolated, and reverse transcription is performed, to generate cDNAs. These cDNAs are labelled with fluorescent tags, and introduced to the array, allowing them to hybridize with any complementary DNA sequence they can find.
Now recall that these cDNAs will have sequences that should be identical to segments of the genes that produced the mRNAs, because DNA is the template for the mRNA during transcription, and the mRNA is the template for the cDNA During reverse transcription.
One of the two strands of some cDNA molecule made from an mRNA ought to bind to the DNA fragment in the particular well that can produce that mRNA in the first place, since they will be highly complementary, and once time is given for hybridization to take place, any cDNA that exhibits little to no binding is washed away.
Wherever binding has occurred, this is indicated by the fluorescence of the cDNA, and is clearly visible. If we label different samples with different colors, such as different tissue samples, we can then get an enormous amount of qualitative data all at once.
In above image everywhere we see one color, such as red, red cDNAs are bound, meaning that particular gene is expressed in the tissue that we labelled red. Where we see green, that gene is expressed in the tissue that we labelled green. If we see yellow, that means both the red and green cDNAs are binding, so we see the intermediate yellow color, indicating that the gene is being expressed in both tissues. And if we see little to no coloring, the gene is not expressed in either tissue, and no binding will occur.
This technique is immensely useful in a variety of contexts. Say we want to know how gene expression has been altered in a cancer cell. We can compare the mRNAs in a regular cell and a cancer cell on the same array, and as simply as identifying a color on a grid, we can know precisely which gene has been altered. Then we can just sequence that gene and know precisely where mutation has occurred, and therefore get information about how the resulting protein has been altered, which allows us to understand on a fundamental level why the cancer is occurring, and suggest new approaches for treatment. There are at least a dozen other common applications of this technique as well, which have a range of utilities. All of this makes the DNA microarray assay an indispensable tool in the molecular biology laboratory.
