Genes evolve over eons by natural selection. If one starts manipulating them, would nature not rebel? Is there a limit to exploit the knowledge of genes to suit the goals by those superior in the nature’s hierarchical ladder, the homosapens?
The major beneficial impact of genetic research was realised when Genentech announced the production of genetically engineered human insulin in 1978. The insulin produced by bacteria was approved for release by the Food and Drug Administration of USA in 1982. The prices of this life saving drug drastically reduced since then. Another breakthrough was in the drug research: Genetically modified mice are not aware opthe defacto standard for the study and modelling of cancer, obesity, heart disease, diabetes, arthritis, substance abuse, anxiety, aging and Parkinson disease. Also genetically modified pigs have been bred with the aim of increasing the success of pig to human organ transplantation.


Genetic research entered paradigm shift when Gene editing became a reality. The gene editing tool known as CRISPR catapulted into scientific laboratories and headlines only a few years ago. Clustered regularly interspaced short palindromic repeat (CRISPR)-Cas systems are well-known acquired immunity systems that are widespread in archaea and bacteria. The RNA-guided nucleases from CRISPR-Cas systems are currently regarded as the most reliable tools for genome editing and engineering. The first hint of their existence came in 1987, when an unusual repetitive DNA sequence, which subsequently was defined as a CRISPR, was discovered in the Escherichia coli genome during an analysis of genes involved in phosphate metabolism.
This year’s chemistry Nobel was awarded to Emmanuelle Charpentier and Jennifer Doudna for their work on CRISPR, a method that can cut up DNA in an organism’s genome and edit its sequence, the genetic “instructions” that determine how an organism will develop. CRISPR is currently making a huge impact in health: There are clinical trials on its use for blood disorders such as sickle cell disease or beta-thalassemia, for the treatment of the most common cause of inherited childhood blindness and for cancer immunotherapy. It is literally a ‘cutting edge’ technology today.
The Regeneron cocktail that was recently administered to president Trump, has fully-human antibodies produced by the mice, which have been genetically modified to have a human immune system, as well as antibodies identified from humans who have recovered from COVID-19.
Fast on its heels of gene editing came the reemergence of a profoundly consequential controversy: Should these new techniques be used to engineer the traits of future children, who would pass their altered genes to all the generations that follow? This is not an entirely new question. The prospect of creating genetically modified humans was openly debated back in the late 1990s, more than a decade and a half before CRISPR came on the scene and several years before the human genome had been fully mapped.
The use of gene-editing in human cases following the first use by Chinese scientist He Jiankui, who made the first genome-edited human babies in 2018. He Jiankui and his colleagues were targeting a gene called CCR5, which is necessary for the HIV virus to enter into white blood cells (lymphocytes) and infect our body. The team wanted to recreate this mutation using CRISPR on human embryos, in a bid to render them resistant to HIV infection, the father being HIV positive. But this did not go as planned and they generated different mutations, of which the effects are unknown. The twin girls were delivered by the mother, may or may not have been conferred HIV resistance, and may or may not have other consequences.
Editing the genes of an embryo is not enough to create a designer baby. The embryo would need to be viable, and working with viable embryos — one that can actually develop into babies — is a whole new step that many countries would not allow. But if someone were to do this work on viable embryos, implant them in a hospitable womb in a fertility clinic, and let them be carried to term, that would effectively create a person with genetically modified DNA that they’d then be able to pass on.

During the same millennial shift, policymakers in dozens of countries came to a very different conclusion about the genetic possibilities on the horizon. They wholeheartedly supported gene therapies that scientists hoped (and are still hoping) can safely, effectively, and affordably target a wide a range of diseases. But they rejected human germline modification—using genetically altered embryos or gametes to produce a child—and in some 40 countries, passed laws against it. There are 29 countries had an outright legal ban on genetic editing. In China, India, Japan, and Ireland, bans existed but didn’t necessarily have legal enforcement mechanisms behind them. In the case of China, the group who announced their famous results in April was able to get permission to work with non-viable embryos that could never have been brought to term; that’s how they worked within China’s guidelines. The US a special case, where the NIH has a moratorium on this research. Other countries have ambiguous rules.
Direct genetic engineering in the food industry has been controversial ever since its introduction. The successful completion of two decades of commercial GM crop production (1996–2015) is underscored by the increasing rate of adoption of genetic engineering technology by farmers worldwide. With the advent of introduction of multiple traits stacked together in GM crops for combined herbicide tolerance, insect resistance, drought tolerance or disease resistance, the requirement of reliable and sensitive detection methods for tracing and labeling genetically modified organisms in the food/feed chain has become increasingly important. The most widely accepted genetically modified traits in GM crops are herbicide tolerance and insect resistance. GM soybean, maize, canola, and cotton are the most common examples of these crops in the market. Developing countries like India and China are the largest producers of genetically modified Bt cotton. The development of a newer dicamba and 2,4-D tolerant crops as an update of older version, exposes that despite contradicting the warnings of environmentalists, corporations were actively preparing for the emergence of superweeds. The introduction of these new herbicide tolerant crops is an admission of failure. It also represents a colossal failure of imagination in dealing with the cycle of problems in chemical-GM farming. The biotech industry is committed to addressing the problems that GM creates with new GM products rather than with actual solutions.
For 10 years, the company Oxitec has been testing whether genetically modified mosquitoes can suppress populations of their natural brethren, which carry devastating viruses such as Zika and dengue. Its strategy: Deploy (nonbiting) male Aedes aegypti mosquitoes bearing a gene that should doom most of their offspring before adulthood. Now, a team of independent researchers analyzing an early trial of Oxitec’s technology is raising alarm—and drawing fire from the firm—with a report that some offspring of the GM mosquitoes survived and produced offspring that also made it to sexual maturity. As a result, local mosquitoes inherited pieces of the genomes of the GM mosquitoes. There’s no evidence that these hybrids endanger humans more than the wild mosquitoes or that they’ll render Oxitec’s strategy ineffective. “The important thing is something unanticipated happened,” says population geneticist Jeffrey Powell of Yale University, who did the study with Brazilian researchers. “When people develop transgenic lines or anything to release, almost all of their information comes from laboratory studies. … Things don’t always work out the way you expect.”
Should the scientific pursuits and new knowledge frontiers not allow their exploitation for healthier life? Could the present day fertility clinics produce ‘designer babies’ in the future? Should it serve to increase the food production? Or Would it be construed as interfering with the God’s nature by the society?
So far this Million dollar question has not been answered yet, right?
Credits:
1. History of CRISPR-Cas from Encounter with a Mysterious Repeated Sequence to Genome Editing Technology: Yoshizumi Ishino, Mart Krupovic, Patrick Forterre
https://jb.asm.org/content/200/7/e00580-17