Using Genetics and Biotechnology to Benefit Humans and Animals
Based on Dr. Dechows talk
Danling Ye
Biotechnology has already been used to further agricultural and medical fields. Genetic engineering, a form of biotechnology, is a powerful tool because it allows scientists to actively manipulate genes the building blocks of proteins that determine much of an organisms characteristics by either adding or removing DNA to the organisms genome. In the future, scientists will continue to use biotechnology and genetic engineering to improve animals. Soon, it may be possible to have pain-free animals, obtain human milk from cows, and banish menopause through biotechnology. 1,2,3
Using biotechnology to produce animals that do not feel pain could make raising livestock more humane and mitigate some of the opposition to eating meat. Scientists have already learned much about the brains response to pain and have done experiments with mice in which they were able to eliminate pains unpleasantness, but not its sensation. 1 They have discovered that the brain has two separate pathways necessary for pain perception: a sensory pathway, and an affective pathway that determines the pains unpleasantness. 1 The anterior cingulate cortex is important in the bodys perception of pains unpleasantness, and by genetically engineering mice so that they lack certain proteins involved in the operation of the anterior cingulate cortex, scientists have developed mice that do not become hypersensitive to painful stimulus, but will still react to a painful stimulus. 1 For example, Zhuo and colleagues have identified cellular mechanisms of pain-related activity in the anterior cingulate cortex and some key features that are needed so that long-term potentiation a process resulting in the enhancement of connections of two neurons through simultaneous stimulation can occur. 4 The presence of extracellular-regulated kinases, the presence of mGluR1 subreceptor, and the presence of adenyl cyclases AC1 and AC8 that respond to Ca 2+
and lead to the production of cAMP, a second messenger, are all involved in long-term potentiation. 4 Blocking the processes involved in long-term potentiation leaves acute pain intact, but reduces persistent and chronic pain. 4 In another experiment done by Feng Wei et al., the scientists were able to create knock-out mice that lacked the enzymes AC1 and AC8. 4 The mice had normal responses to tests of acute pain, but had reduced responses to persistent pain as compared to mice in a control group. 4 If the pain-reducing technology used in mice can be applied to agriculture animals, meat products can be produced more humanely. In addition to producing pain-free animals, biotechnology can be used to develop cows that produce milk similar to human milk. Scientists have genetically engineered cows to produce milk with lysozyme, an antimicrobial human protein found in human milk, lactoferrin, which boosts the number of immune cells in babies, and alpha-lactalbumin, another milk protein. 2 Professor Li and colleagues have done research showing that it is possible to humanize cow milk, which could be extremely beneficial to babies in the future. 2 The currently available baby milk formula is often criticized for not being an adequate substitute for human breast milk, but humanized cow milk could be a healthy substitute to breast milk. In addition, transgenic cows could produce milk with biopharmaceutical properties on a large-scale. 5 Currently some individuals have ethical objections to introducing humanized cow milk and oppose genetically engineering organisms in general. In addition, problems with the technique used to genetically engineer the cows resulted in the death of some of the transgenic cows in Professor Lis study. 2 However, as biotechnology advances, humanized cow milk or biopharmaceutical cow milk might become widely available to the public. Biotechnology also could be used to help older women. A team of researchers at Edinburgh University, working in conjunction with a team from Harvard Medical School, were the first to be able to grow egg cells from laboratory stem cells. 3 Previously, scientists have used embryonic stem cells, which are derived from the early embryo and can grow indefinitely and remain pluripotent if placed under the right conditions, to produce different types of somatic cells. 6 However, producing egg cells was a breakthrough because it had never been done before; gametic cells are harder to produce from stem cells than somatic cells. Producing egg cells from stem cells could potentially have tremendous benefits; stem cell based rejuvenation of oocyte reserves in ovaries could help older women decrease their risk of developing many age-related health diseases, such as osteoporosis, cardiovascular disease, and cognitive dysfunction. 7
As scientists further study animal genetics and improve biotechnology, they will find more ways to use their knowledge to produce animals with desirable characteristics, enhance human medicine, and improve agriculture. Through advances in biotechnology, farm animals could live healthy, pain free lives, babies could drink healthier milk from cows, and women could live longer. Only time will tell how the discoveries of today will be used in the future.
Bibliography 1) Shriver, Adam. "Not Grass-Fed, but at Least Pain-Free." The New York Times. The New York Times, 18 Feb. 2010. Web. 27 Apr. 2014. 2) "Genetically Modified Cows Produce 'human' Milk." The Telegraph. Telegraph Media Group, 02 Apr. 2011. Web. 27 Apr. 2014. 3) Connor, Steven. "Scientists Rewrite Rules of Human Reproduction." The Independent. Independent Digital News and Media, 07 Apr. 2012. Web. 27 Apr. 2014. 4) Shriver, Adam. "Knocking Out Pain in Livestock: Can Technology Succeed Where Morality Has Stalled?" Neuroethics 2.3 (2009): 115-24. Print. 5) Berkel, Patrick H.c. Van, Mick M. Welling, Marlieke Geerts, Harry A. Van Veen, Bep Ravensbergen, Mourad Salaheddine, Ernest K. J. Pauwels, Frank Pieper, Jan H. Nuijens, and Peter H. Nibbering. "Large Scale Production of Recombinant Human Lactoferrin in the Milk of Transgenic Cows." Nature Biotechnology 20.5 (2002): 484-87. Print. 6) Pera, M. F., B. Reubinoff, and A. Trounson. "Human Embryonic Stem Cells." Journal of Cell Science (2000): 5-10. Print. 7) Tilly, J. L., and E. E. Telfer. "Purification of Germline Stem Cells from Adult Mammalian Ovaries: A Step Closer towards Control of the Female Biological Clock?" Molecular Human Reproduction 15.7 (2009): 393-98. Print.