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Transcript
Biological
Sciences
Initiative
HHMI
Using Microarrays to Study Leukemia
Diagnosis of ALL vs AML using microarrays
There is a good high school level activity online that includes use of microarrays to
diagnose ALL vs AML. It is found as part of the packet entitled “DNA Chips: A
Genetics Lab in the Palm of your Hand”
How this type of microarray works
The Gene Chip
In this lab, the microarray used is a commercial gene chip. Each spot on the slide (or
microarray) is a single stranded DNA sequence from a different human gene. Scientists
originally used a gene chip that contained 6,187 genes, one gene per spot. In the minimicroarray you view in this activity, they have selected 25 genes of interest and you will
see results from only these 25 genes.
The Samples
The goal is to compare the gene expression (genes that are turned on) in white blood cells
from ALL vs AML vs non-leukemia patients. Remember that when a gene is expressed,
it is transcribed and an mRNA is made.
Messenger RNA is isolated from the white cells of a leukemia patient. The mRNA is
used as a template to synthesize complementary single strand DNA (cDNA). The cDNA
is made with a fluorescently labeled nucleotide. In this case, only one color radioactive
label (red) is used. The resulting product is cDNA for each of the genes expressed in the
white cells of the leukemia patient.
University of Colorado • 470 UCB • Boulder, CO 80309-0470
(303) 492-8230 • Fax (303) 492-4916 • www.colorado.edu/Outreach/BSI
This cDNA probe is then allowed to anneal to the microarray, one person’s cDNA per
microarrray. The labeled fluorescently labeled cDNA will bind to each of the human
genes that are expressed in the white cells of that patient. A laser is then used to
determine which genes had bound the labeled cDNA. If a given gene is expressed, the
labeled cDNA corresponding to that gene will bind, and the spot where the gene is will
light up red.
Gene that is not expressed (blank spot)
Gene that is expressed (red spot)
Scientists originally annealed the cDNA probes to microchips containing 6178 human
genes. One patient’s probe on one microchip. They then used a computer to compare the
results for all 6178 genes between many ALL, many AML, and many non leukemia
samples as well. They were able to identify sets of genes that are expressed only in ALL
or only in AML.
For this activity a subset of 25 genes was selected. These genes are listed in the handout
and are expressed in AML patients, in ALL patients or are control genes. Positive
control genes should be expressed in all samples, and negative control genes should not
be expressed in any sample.
The activity
A printable teachers guide and student activity can be found at
http://science-education.nih.gov/newsnapshots/TOC_Chips/Chips_RITN/chips_ritn.html
The name of the package of activities is
“DNA Chips: A Genetics Lab in the Palm of Your Hand”
You can use this title to search for the activity if the URL has changed.
So what? Where do we go from here?
Above you saw the use of the microarray to diagnose ALL vs AML. We could already
do this prior to the advent of microarrays. So what new information and abilities does the
microarray allow?
• Diagnosis - We now know all the genes that are differentially expressed between
the two types of leukemia allowing the development of additional (potentially
improved) diagnostic tests.
• Tumor classification - We will be able to address whether different subtypes of
cancers exist within AML and ALL.
• Treatments - The differing gene expression profiles can be used to design
additional leukemia and patient-specific treatments.
• Basic Science - The differing gene expression profiles will give us insights into
the cellular processes leading to and resulting from these leukemias.
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