Gene Editing Pros And Cons

CRISPR is a new gene-modifying tool that has the potential to treat numerous medical conditions by editing genes that are responsible for certain diseases. This technology is based on the ability of bacteria to destroy the DNA of invading viruses. Studies have suggested that this new technology can be applied to human cells, although the idea of chopping up regions of the human genome can be unethical and could even be harmful. In order for the treatment to be administered to a patient, a small piece of RNA and an enzyme that makes a cut in the DNA are delivered to the cells. A biotechnology company, known as Editas Medicine, located in Cambridge, MA, is already designing treatments for conditions of the blood and the eye using CRISPR. For

Genome editing is a huge leap forward in science and medicine. Because of recent advances in technology, the study of genes and induced ‘point’ mutations have led to the discovery and advancement of methods previously used in order to mutate genes. The development of Clusters of Regularly Interspaced Short Palindromic Repeats (CRISPRs) and CRISPR associated system 9 protein (Cas9) technology is a hugely significant leap forward as this is a tool that could potentially be used for the research into and hopefully the treatment of a range of medical conditions that are genetically related. Cystic fibrosis (Schwank, G. et al, 2013), haemophilia and sickle cell disease are an example of some of the conditions that have the

Why are humans stuck how they are? Why do some have lethal flaws? Why do theses flaws exist? The correct answer is they don’t have to: Human genetic engineering can solve some of theses lethal issues now and can solve more in the future. It can help the next generation experience what everyone strives to achieve. Human genetic engineering research should continue because it can save people's lives, improve human’s lives and improve the lives of the next generation of children.

With modern technology comes the breakthrough of the decade by altering the human genes. This altering gene invention is called CRISPR/Cas9. However, this invention in the beginning stages of altering genes, began with rats until perfection. The process began early with the embryo stages to edit the genes. With the introduction of CRISPR surrounds a lot of controversy. Some people believe editing genes is playing with the hands of God and refuse to believe in CRISPR. With the article, “Let’s Hit Pause Before Altering Humankind”, by David Baltimore believes CRISPR is a tool with no good intentions. With this information the article should not be published with being against CRISPR.

Australia should not legalise the genetic modification (or GM) of human embryos. Australia should keep genetic modification of human embryos illegal because if we allow genetic modification to embryos it could lead to some babies DNA having been carefully selected to enhance their appearance, intelligence or something that is not a normal thing to have chosen. These enhancements may also be unevenly distributed among the population, leading to a society of genetic haves and have-nots. One side is to allow genetic modification to embryos and take out diseases that run in family blood lines. The other side is against the genetic modification of embryos mainly because people do not want want people who are all perfect for one thing

Worryingly, there has been minimal public debate regarding this technology that could irreversibly alter the human race. Instead, ethical discourse has been largely contained to scientific and political circles. It is extremely problematic that a large majority of the general public is unaware of the research and debate regarding human gene modification. In addition, the current debate has stagnated, with researchers and politicians being unable to find any common ground. However, upon close examination of the three main ideological groups within this controversy, a key similarity becomes apparent: each group, regardless of whether they are proponents or opponents of human gene

Genome editing is still relatively new in the science world. It was only fairly recently that we gained the first ability to fix our DNA (Rajan). Genome editing is changing the DNA, which gives us the ability to change it for the better – which is not an easy thing to do (What Is Genome Editing?). In order to change the DNA, clustered regularly interspaced short palindromic repeats (CRISPR) are manipulated to improve the DNA (Hornblower, Reis, Robb, and Tzertzinis). A fracture is made in the DNA to modify it, in order to adjust the DNA to try to rid it of genetic diseases and abnormalities (What Is Genome Editing?). Then, a new sequence can be added into the existing DNA and be repaired (What Is Genome Editing?). This is the basic idea of the difficult genome editing. While complicated, once more progress is made and it becomes more successful, this process could work on a variety of diseases (What Is Genome Editing?).

In recent years genetic modification has been advancing. Genetic modification is when a living organism has been altered to a specific state of characteristics. So far scientist has made one attempt to modify genes from an embryo recently. Whether they were successful or not is question unanswered yet. Gene modification can be great and all. However, is it right to modify genes? Apparently, the population agrees to modify genes since there has been licenses of approval for gene modification. If Society cared about gene modification, then there would be signs of disapproval of gene modification. However, this is viewed morally wrong in my point of view. The pros of modifying genes are that defeating diseases, potential to live longer, genetic diseases, and able to select character traits of babies. The cons of modifying genes are failures on the way to perfecting genetic modification, genetic modification babies can have more greater problems, very expensive, and when does it stop?

There are other types of gene editing out there but research shows us that CRISPR is fast, precise, and simple. Researchers are developing a way for CRISPR therapy to help with Alzheimer’s all the way to HIV. There are two categories the researchers and people have put CRISPR in: practical and philosophical. The researchers say that the immediate barrier is practical. During the tests, CRISPR has found targets in other parts of the DNA that need fixing other than the intended part of the DNA. Because of this, it may take at least a generation to ensure that it is safe. Some people oppose CRISPR because the oppositionists say it lets people play god but getting medicine every time you get sick with the same thing obscures the natural order of things. The opportunities are getting pushed ahead for treating cancer, childhood diseases that are genetic, and how to understand diabetes better. The one question some people have is whether it’s right to edit genes that are

Imagine the possibility of eliminating serious genetic diseases from the world. Imagine the idea of treating, preventing or even curing diseases that are yet to be cured. Imagine the feeling of being given improved health and a prolonged lifespan. This can all be accomplished with the aide of genetic engineering. Human genetic engineering refers to the process of directly manipulating human DNA to produce wanted results. DNA is a simple but very complex chemical that has the power to change the world and has begun to do so already. Many opponents to gene therapy fail to realize that genetic engineering has great potential to become very important in the biomedical industry. Though controversy exists regarding the ethics of human genetic engineering, it can produce numerous benefits, which outweigh its disadvantages and side effects; therefore, scientists should be able to manipulate the human genome for the purpose of helping people with serious medical conditions.

Throughout the world, many intelligent minds exist. One, in particular, had something to say about Human genetic engineering. “Nuclear weapons need large facilities, but genetic engineering can be done in a small lab. You cannot regulate every lab in the world. The danger is that either by accident or design, we create a virus that destroys us” (Stephen Hawking). Hawking is considered to be one of the most intelligent people in the modern world. For this reason, his statement is not to be taken with a grain of salt. The concept of Human genetic engineering is surrounded with danger and controversy. There are several different positions on human genetic modification. Conservatives, or Traditionalists believe such innovation or change would be detrimental towards the human race. Conservatives say that families are the foundation of society so changing how families come to be would ultimately tear society apart (Foht). Others say that innovation of such magnitude would act as a boon to the human race. Concerning the danger of genetic engineering, it could definitely become an immense detriment. However, with the correct limitation and government oversight, the human race will benefit from it. Genetically engineering a Human embryo is a step that science will eventually take. Whether it be decades or centuries from now, genetically modified humans will walk the Earth.

Human gene editing has long been controversial topic; however, precise techniques that accomplish this feat have only recently been discovered. According to the Welcome Genome Campus in the UK, the most versatile and simplest technique, called CRISPR-Cas9, allows scientists to cut, alter, or add to sections of the DNA sequence of living organisms (“What Is CRISPR-Cas9?”). This astonishing technology has nearly endless applications, including the potential to eradicate genetic diseases in humans that currently have no cure. This could have vast implications for people who suffer with disease and the economy of the region in which they live, but the technology has yet to be commercialized. The

John Harris and Marcy Darnovsky’s article, Pro and Con: Should Gene Editing Be Performed on Human Embryos? (2016), explores the potential moral and future repercussions involved with CRISPR-Cas9 gene editing, a rapidly growing science. Harris argues that gene editing could be the resolution to curing detrimental illnesses before the birth of a child, and the science needs more time to experiment. On the other hand, Darnovsky argues that while gene editing may be able to treat illnesses before birth, it opens the door for parents to decide what they want their children to be like and to get rid of any undesirable traits. Both authors appeal to the audience’s logos to argue for or against gene editing and its potential consequences. Harris states

New technological advances and scientific methods continue to change the course of nature. One of the current controversial advances in science and technology is the use of genetically modified embryos in which the study exceeds stem cell research. Scientists have begun planning for research involving human embryos in the genetic modification field. Many technological developments are responsible for improving our living standards and even saving lives, but often such accomplishments have troubling cultural and moral ramifications (Reagan, 2015). We are already beyond the days in which virtually the only procreative option was for a man and a woman to conceive the old-fashioned way (Reagan, 2015). Genetic modification of human embryos can be perceived as a positive evolution in the medical process yet it is surrounded by controversy due to ethical processes. Because this form of genetic modification could affect later born children and their offspring, the protection of human subjects should be a priority in decisions about whether to proceed with such research (Dresser, 2004). The term Human Genetic Engineering was originally made public in 1970. During this time there were several methods biologists began to devise in order to better identify or isolate clone genes for manipulation in several species or mutating them in humans.

Genetic engineering is the process whereby new DNA is added or existing DNA is altered in an organism 's genome. This may involve changing one base pair (A-T or C-G) or deleting entire sections of DNA or adding additional copies of a gene. This results in creating new traits that were not previously present in the organism’s genome. This is done to selectively breed desired traits or to create plants with increased resistance to pesticides and increased tolerance to herbicides. For example insulin is a protein that regulates sugar content in our blood and is produced normally in the pancreas. Genetic engineering is used to produce a form of insulin that is similar to yeast and bacterial cells. This genetically engineered insulin is called