Recombinant DNA technology not only revolutionized scientific research but also triggered the birth of the private sector biotechnology industries. It involves combining genetic material from different organisms to obtain desirable phenotypes. This technology has opened numerous avenues in medicine, basic research and industry. It also gave rose to as many concerns.
Organisms thus
modified could interact with non-modified, wild populations and bring about
unpredictable changes risking environment and public health. The Asilomar Conference on
Recombinant DNA held in 1975 brought
scientists, lawyers and physicians together to establish guidelines and
restrictions to be imposed on rDNA. It enlisted precautions regarding containment,
good handling practices and restrictions on experimenting with infectious
organisms to prevent any major accident.1
The
science of rDNA continues to be applied in different contexts.
rDNA
Today:
At the time of the
Asilomar conference, there was no practical application of rDNA. Today, rDNA is
used in the production of high yield, high nutrition GM crops, in production of
vaccines, hormones and medicines, bioremediation, environment friendly energy
sources and gene therapy.2,3 All of these applications of rDNA have
been controversial with safety concerns bringing the discussion into public
domain.
The case of He Jiankui a researcher in Shenzhen, China using CRISPR on human embryos to provide immunity against
HIV awakens us to the many undesirable results of such experiments.4
This necessitates us to reconsider the potential
hazards in the 21st century and how it can be avoided. A revision of guidelines and precautions seems to be
necessary. The following discussion aims to do the needful.
Medicine and gene therapy:
Drugs
developed through rDNA should pass through several layers of scrutiny and
testing before being prescribed. Testing the drugs on non-target systems can
further help identify potential side effects.
Gene
therapy must be strictly regulated as intergenic interactions are not well
understood. The effect of any modification elsewhere in the body cannot be
predicted. It should be particularly avoided at the embryonic stage. Germ line
modifications can be inherited and might make containment difficult. It could
introduce new diseases into the population, spring a demand for “designer
babies” and could be used by anti-social elements in numerous ways.
Genetically Modified (GM)
crops:
GM
crops and foods need to undergo thorough evaluation before being brought into
market. Genetic modification on one locus may bring changes in non target
locus. These changes may include increased production of compounds which may be
toxic to the consumer.
A
very well known example of introduction of GM crops leading to ecological
complications is that of the effect of loss of a weed called milkweed on
numbers of Monarch butterflies. Producing GM pesticide resistant crops allowed
farmers to use huge amounts of pesticide on weeds leading to a drastic decline
in milkweed numbers which is the primary food source for Monarch butterflies.5
It is an example of how caution should always be exercised when bringing in
changes in the environment. Such GM crops are responsible for the increase in use of herbicide by 527
million pounds in the U.S. over 16 years of their commercial use. This has
stimulated the production of herbicide-resistant weeds and increased water pollution
by runoff herbicides.
Thorough
Environmental Impact Assessment is necessary before introducing GM crops into
the environment. Research needs to be redirected in finding better solutions to
food production than making pesticide resistant crops.
Containment:
Conventional
farmers are exposed to the risk of their crops being contaminated by transgenic
pollen drifting from the GM fields. Such spill over has happened in the US with
Monsanto’s crops and a farmer was accused of growing GM crops without permits.
This is a depiction of how GM crops have social effects apart from economic,
health and environmental effects.7
Such containment
issues exist in case of all GM organisms- from plants and bacteria to humans.
Utmost prudence needs to be exercised when permitting rDNA experiments on any
organism. Only after the research group or institution has demonstrated their
ability to contain such organisms and have clarified their intent of use and
extent of modifications should rDNA experiments be permitted.
Repercussions for
not adhering to norms must be dire to discourage malpractices. This includes
consequences for the research group, institute as well as the country. Misuse
of rDNA technology has global implications and hence countries must closely
monitor such research.
In conclusion,
strict norms and constant regulation can avert and mitigate any disasters
resulting from the use of rDNA technology.
References:
1.
Paul
Berg, et al. (1975). Summary
Statement of the Asilomar Conference on Recombinant DNA Molecules*. Proc. Nat. Acad. Sci., USA. (June)
72(6)1981-1984.
2.
Suliman Khan, Muhammad Wajid Ullah, Rabeea Siddique, et al.,
“Role of Recombinant DNA Technology to Improve Life,” International
Journal of Genomics, vol. 2016, Article ID 2405954, 14 pages, 2016. https://doi.org/10.1155/2016/2405954.
3.
Charles
R. Cantor. (2000). Biotechnology in the 21st century. TIBTECH (January) 18.
5.
https://actions.sumofus.org/a/monsanto-is-killing-the-monarchs
6.
https://en.wikipedia.org/wiki/Biocontainment_of_genetically_modified_organisms
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