Beruflich Dokumente
Kultur Dokumente
Gracey Sorensen
Global History 2
Mastroianni
3 March 2017
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Imagine being able to assure that your newborn child was to be born as healthy as can be
and disease free. Imagine being able to manage chronic diseases and continue to live the life you
always wanted. The future is now and technology is only improving in order to make these
identify specific genes, remove them, and clone (duplicate) them and use them in another part of
the same organism, or in an entirely different one ("Medical Discoveries). The popularity of
genetic engineering only continues to grow as there are more discoveries regarding medicines
and medical abilities. Genetic engineering is beneficial due to its impact on medicine, treatment
to babies and many terminal illnesses, and many advancements that are yet to come.
medicines. Pharmaceutical medicines are medicines sold and made through pharmacies, many
being made from recombinant DNA. Recombinant DNA is the process of removing DNA from
one organism and inserting it into the DNA of another organism, giving it new traits. This
process allows for the development of drugs, vaccines, and the ability to reproduce important
human hormones and proteins (DNA). The exact process includes first finding the wanted
gene sequence and then using the polymerase chain reaction technique to make perfect copies of
DNA fragments. (Medical Discoveries). In other words, scientists use a piece of RNA to copy
the wanted DNA and make the new gene. By engineering human DNA into a host organism, that
organism can be turned into a factory for important medical products. This technique allowed
for the ability to make so many pharmaceuticals including medicine to treat, factor VIII for
males suffering from hemophilia A, factor IX for hemophilia B, erythropoietin (EPO) for
treating anemia, several interleukins, tissue plasminogen activator (TPA) for dissolving blood
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clots, adenosine deaminase (ADA) for treating some forms of severe combined
immunodeficiency (SCID), and so many more (DNA). The most commonly known
genetically engineered medicine is insulin, which treats both type 1 and type 2 diabetes. The
production of insulin itself has changed the life of 1.25 million Americans, including about
200,000 children ("Type 1 Diabetes Facts). Chronic diseases have been much easier to adapt to
thanks to the immense amount of growth in the medicine and treatment industry due to genetic
engineering. According to the Centers for Disease Control and Prevention (CDC), as of 2012,
almost half of all adults, 117 million people, have had one or more chronic health issues. One of
four adults had two or more chronic health conditions ("Chronic Disease Overview). Most of
these conditions made so much easier to adjust to because of the genetic engineering process in
pharmaceuticals. Pharmaceutical medicine have changed the lives of so many people around the
world and the abilities they have only continue to grow as more advances are made.
Genetic engineering is also beneficial due to its ability to help serious and terminal
illnesses. In 2012, a research team led by Jennifer Doudna and Emmanuelle Charpentier
discovered a gene editing tool which took the world by storm. The CRISPR-Cas9 is a gene
editing tool which has the ability to remove gene mutations and produce the correct or desired
gene sequence. Bacteria have developed a defense system against DNA sequences called
CRISPR (clustered regularly-interspaced short palindromic repeats) and now the CRISPR-Cas9
protein is a scientific breakthrough which allows for any gene sequence to be edited and
modified (Murnane). When relating to bacteria and diseases, the process in which it works has
discovered as surprisingly simple. The treatment first includes discovering the harmful DNA
sequence that needs to be removed from the cell. Then two RNA with the matching DNA
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sequences join with the Cas9 protein in order to form a complex that has the capability to cut
DNA sequences. Once the complex attaches itself to the harmful DNA, the guide RNA will find
the harmful genome and be able to cut the DNA, paralysing it and making it no longer harmful to
the cell (Murnane). Before CRISPR-Cas9, gene editing was much more dangerous due to the
lack of precision, and when dealing with genes, accuracy is key in order to make a safe
transformation and not from new mutations in the process. Also, the old practices cost thousands
of dollars and a range from weeks to months in order for the gene to be changed, the
CRISPR-Cas9 will be able to accomplish the wanted correction in hours and has an estimated
cost of seventy-five dollars (Murnane). This extreme advancement in the medical field will
allow for so many more patients all over the world to get the treatment they need in order to be
free from many terminal illnesses. The CRISPR-Cas9 has had a large focus on working to cure
sickle cell anemia, cystic fibrosis, muscular dystrophy, huntington's disease, and certain forms of
Alzheimers. There are thought to be cures to these and many more in the near future. The gene
editing tool will be able to work in both cultured and living cells, and on every organism,
including animal or plant, that it has been tested on (Murnane). One of the most amazing aspects
of the CRISPR-Cas9 discovery is that when discovering this gene editing tool, the scientist also
discovered the ability to reverse the changes made. This discovery is called the anti-CRISPR
proteins that can be used to control the use of CRISPR-Cas9 tool. One of the most dangerous
aspects of the gene editing is that the CRISPR-Cas9 may produce gene edits that are unintended.
According to Kevin Murnane, a cognitive scientist and author for Forbes magazine, Researchers
can reduce or eliminate these unintended edits by using the anti-CRISPR proteins to shut the
CRISPR-Cas9 system down after the intended gene edit is completed (Murnane). This is such
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an important aspect due to the level of security it adds to the process and will allow for much
more life changing DNA edits. The testing and discovery of CRISPR will be a huge addition to
In the future, genetic engineering will only continue to advance, affecting the health of
.babies. Pre-birth testing is the action of doctors testing genes in the cells of embryos for genetic
mutations. This assures that the embryo is safe and the baby will be born free from disease and
deformations (Lerner). According to Anne Matthews, RN, PhD, associate professor of genetics
in the school of medicine at Western Reserve University, approximately 4 million babies are
born each year and between 3-4% will be born with a genetic disease or major birth defect
(Matthews). Also, birth defects happen to about 3% of all babies born in the United States
("Data & Statistics). The new technology available to test the genes will help so many families
who have genetic disorders passing down from generation to generation. Additionally,
researchers have also recently discovered yet another way to improve the health of newborn
babies with the use of in-vitro fertilization, also known as mitochondrial transfer. This is the
process of combining the sperm and egg cell in a laboratory and testing for mutations before
being reimplanted into the woman to grow (Lerner). In todays world too many children are lost
and forced to suffer due to genetic mutations. Being able to prevent these diseases will help so
many families in all countries. Also, another new form of in-vitro fertilization includes the
involvement of three parents, to assure the baby is healthy. It is a known fact that most genetic
mutation are a result from the mother's mitochondrial DNA. An estimated 1 in 5,000 people
carry mitochondria with mutations leading to blindness, diabetes, dementia, epilepsy and
multiple other impairments. By focusing on the genetic level of the parents, if one of the parents
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have a mutation that can be passed on, the scientist will use an egg cell from a prospect mother
(DiSalvo). This idea would theoretically be able to free newborns from any mutations at the
cellular level, however it also brings many new struggles. The UK hopes to realize this law in
July, but the US seems to be much more hesitant based upon all the bioethical issues it relates
(DiSalvo). With these discoveries being so new, much testing is needed and complications to be
figured out before researchers can use these techniques for everyday treatment. It is evident that
all these new forms will allow for the future of babies all over the world to be born much
healthier and can help to cure and diminish so many terminal and chronic diseases millions of
Although genetic engineering shows many benefits for the majority of the population, it
also brings on many fears from the general public. One of the most common fears is relating
eugenics, the science of improving the human race by controlling desirable characteristics
(Lerner). The ability to change genetic code to help diseases, has a direct correlation to being
able to change any genetic code to form any desirable trait. This aspect of eugenics has
previously seen through history during the Holocaust which caused 11 million deaths from
innocent people. Many countries fear this aspect and are hesitant to release the information that
allows for the ability to change genetics. This fear has many times resulted in stunting the
release of new discoveries which could sadly be a very good help to many patients if available
for use. Another fear is that the people will abuse the capabilities the new technology has in
order to create superhumans with bizarre traits. At the moment, parents have the ability to
choose the sex of their child and there are many research teams who predict height, hair color,
and eye color choice will be in the near future (Lerner). With all these decisions, the possibilities
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will endlessly grow until families are able to design their own child. There is no way to be
certain that specific individuals will not abuse the purpose. Lastly, genetic engineering has never
ending opportunities, but is a highly dangerous subject. Unless testing on humans, there is no
way to determine the actual affects gene transfer will have on the human body (Lerner).
Long-term effects are also a big question as to know how genes will act if changes have been
made (Lerner). Overall, there are many questions and concerns relating genetic engineering .
These questions and many more can only be answered with more research and testing, however,
the future is bright for many individuals who would benefit from genetic engineering.
The science world will only continue to further develop genetic engineering which will
inevitably create even more ways in which it can be used beneficially. Genetic engineering is
helpful because although it has its fears, it has an immense impact on the health of so many, such
as with pharmaceutical medicines, and the effect it has on terminal illness and babies. When
mentioning the future and thinking about genetic engineering, the words advancement and
improvement come straight to mind. With the help of genetic engineering, death from many
illnesses will become a problem of the past and influence the lives of people all over the world.
Not only does genetic engineering affect adults, it has made progress to affect pre-born babies
and children of all ages with medical issues. In everyones life, at one point or another, they
will be required to deal with the affects of illness and disease. People should give their attention
to genetic engineering and the studies being done in order to make a brighter, healthier future for
the world and the people they love. For many, the future of medicine will determine their life
and everyone needs to understand the importance of using genetic engineering for good, which