Essay About Restriction Fragment Length Polymorphism And Cystic Fibrosis Gene

The Cystic Fibrosis Gene
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Introduction:
Cystic fibrosis is an inherited autosomal recessive disease
that exerts its main effects on the digestive system and the
lungs. This disease is the most common genetic disorder
amongst Caucasians. Cystic fibrosis affects about one in
2,500 people, with one in twenty five being a heterozygote.
With the use of antibiotics, the life span of a person
afflicted with CF can be extended up to thirty years
however, most die before the age of thirteen.1 Since so
many people are affected by this disease, its no wonder
that CF was the first human genetic disease to be cloned by
geneticists. In this paper, I will be focusing on how the
cystic fibrosis gene was discovered while at the same time,
discussing the protein defect in the CF gene, the
bio-chemical defect associated with CF, and possible
treatments of the disease.
Finding the Cystic Fibrosis Gene:
The classical genetic approach to finding the gene that is
responsible for causing a genetic disease has been to first
characterize the bio-chemical defect within the gene, then
to identify the mutated protein in the gene of interest, and
finally to locate the actual gene. However, this classical
approach proved to be impractical when searching for the CF
gene. To find the gene responsible for CF, the principle of
“reverse genetics” was applied. Scientists accomplished
this by linking the disease to a specific chromosome. After
this linkage, they isolated the gene of interest on the
chromosome and then tested its product.2
Before the disease could be linked to a specific
chromosome, a marker needed to be found that would always
travel with the disease. This marker is known as a
Restriction Fragment Length Polymorphism or RFLP for short.
RFLPs are varying base sequences of DNA in different
individuals which are known to travel with genetic
disorders.3 The RFLP for cystic fibrosis was discovered
through the techniques of Somatic Cell Hybridization and
through Southern Blot Electrophoresis (gel separation of
DNA). By using these techniques, three RFLPs were
discovered for CF; Doc RI, J3.11, and Met. Utilizing in
situ hybridization, scientists discovered the CF gene to be
located on the long arm of chromosome number seven. Soon
after identifying these markers, another marker was
discovered that segregated more frequently with CF than the
other markers. This meant the new marker was closer to the
CF gene. At this time, two scientists named Lap-Chu Tsui
and Francis Collins were able to isolate probes from the CF
interval. They were now able to utilize to powerful
technique of chromosome jumping to speed up the time
required to isolate the CF gene much faster than if they
were to use conventional genetic techniques.3
In order to determine the exact location of the CF gene,
probes were taken from the nucleotide sequence obtained from
chromosome jumping. To get these probes, DNA from a horse,