Nuffield Council on Bioethics urges caution on patenting DNAJuly 18, 2002Patents involving DNA sequences should be the exception rather than the rule, according to a paper published today (23 July) by the Nuffield Council on Bioethics. The Discussion Paper, The ethics of patenting DNA, recommends a number of significant changes to the way that patents are granted involving DNA sequences. The Discussion Paper, prepared by an international group of experts, proposes an ethical framework for gene patenting with recommendations aimed at policy-makers, courts, patent lawyers and patent offices. "We are concerned that, for patents involving DNA, the patent system is in danger of not achieving its main goal - to stimulate innovation for the public good. We believe that the Council's recommendations would safeguard against this situation," comments Dr Sandy Thomas, Director of the Nuffield Council on Bioethics. "It is important to question whether patents involving genes could adversely affect healthcare and research," continues Dr Thomas. Diagnostic tests and medicines could become unaffordable or unavailable, the development of new ones might be slowed down, and research could be inhibited. The Paper aims to address these concerns. "The Council calls on patent offices worldwide to work together to examine ways to ensure that the patent system is fairly, but rigorously applied in the case of DNA." Currently, the patent system considers DNA sequences as eligible for patenting, once isolated from their natural environment. "But even if DNA is, in principle, eligible for patenting, it does not mean that each and every application for a patent should be granted" explains Dr. Thomas. At present each application must also satisfy three legal tests: it must be novel, inventive and useful. When applied to DNA sequences, the Nuffield Council argues that these three tests are increasingly problematic. "It is vital that the tests of inventiveness and usefulness should be more rigorously applied," insists Martin Bobrow, Professor of Medical Genetics and one of the authors of the paper. "If this happens, it should substantially reduce the number of patents granted involving DNA sequences." 'Inventiveness' Several types of patents involving DNA would be unlikely to be granted if the test of 'inventiveness' were stringently applied. When a gene is associated with a disease, the DNA sequence can be used as a diagnostic test, for example for breast cancer, or as a target for gene therapy, for example to treat haemophilia. But should that DNA sequence itself be patentable? "We feel that once the link between gene and disease is identified, the use of the gene, for diagnosis or therapy is obvious. It therefore does not fulfil the inventive (or 'non-obvious') test. Patents involving a DNA sequence as a diagnostic test or for gene therapy should rarely be granted," continues Professor Bobrow. "In the case of a diagnostic test, a patent on the use of the sequence may be acceptable, but the patent should be restricted to the particular test specified". 'Usefulness' The Paper recognises that the patent system should reward people for useful new ideas and inventions but argues that, in the case of DNA sequences, the balance is currently too firmly in favour of the claimant. "One specific problem which we considered is the fact that one gene often gives rise to more than one product. This means that it is quite common to find an entirely new use for a DNA sequence after it has been patented. If a patent protects all the uses of a sequence, this can give extensive, and in our view unjustified, rewards to the original researcher," comments Dr Thomas. The Paper notes that some patents that have already been granted are of doubtful validity and makes a number of recommendations to limit the possible adverse effects of these patents. For further information | |||||||||||||||||||||
|
Related DNA Current Events and DNA News Articles Genetic breakdown in Fanconi anemia may have link to HPV-associated cancer A genetic malfunction that causes DNA instability in people with the blood disorder Fanconi anemia may put them at high risk for squamous cell carcinomas linked to human papillomavirus (HPV), according to a study posted online ahead of print by Oncogene. Plants display 'molecular amnesia' Plant researchers from McGill University and the University of California, Berkeley, have announced a major breakthrough in a developmental process called epigenetics. They have demonstrated for the first time the reversal of what is called epigenetic silencing in plants. Research in twins defines shared features of the human gut microbial communities: variations linked to obesity Trillions of microbes make their home in the gut, where they help to break down and extract energy and nutrients from the food we eat. Yet, scientists have understood little about how this distinctive mix of microbes varies from one individual to the next. Tool Helps Identify Gene Function in Soybeans, Could Lead to Better Crop Performance, say MU Researchers In the race for bioengineered crops, sequencing the genome could be considered the first leg in a multi-leg relay. Brown Chemist Finds Gene That Enables Gray Mold to Kill Plant Cells Gray mold is a gardener's nightmare. The fungus, also known by its scientific name Botrytis cinerea, is a scourge to more than 200 agricultural and ornamental plant species, including staples such as tomatoes, strawberries, snap and lima beans, cabbage, lettuce and endive, peas, peppers, and potatoes. Ice beetles impacted by climate change In the summer of 1968, Dave Kavanaugh set off on a hike that would change the course of his life. As a second-year medical student at the University of Colorado, he had joined a climbing club with a few members of the biophysics department, and the group had set their sights on Gray's Peak-the ninth highest mountain in Colorado. Fruit fly research may lead to better understanding of human heart disease Researchers at the Burnham Institute for Medical Research (Burnham) have shown in both fruit flies and humans that genes involved in embryonic heart development are also integral to adult heart function. The study, led by Rolf Bodmer, Ph.D., was published in Proceedings of National Academy of Sciences. CSHL scientists discover a new way in which epigenetic information is inherited Hereditary information flows from parents to offspring not just through DNA but also through the millions of proteins and other molecules that cling to it. Synthetic virus supports a bat origin for SARS SARS - severe acute respiratory syndrome - alarmed the world five years ago as the first global pandemic of the 21st century. The coronavirus (SARS-CoV) that sickened more than 8,000 people - and killed nearly 800 of them - may have originated in bats, but the actual animal source is not known. Scripps Research Scientists Shed Light on How DNA Is Unwound So That Its Code Can Be Read Researchers at The Scripps Research Institute have figured out how a macromolecular machine is able to unwind the long and twisted tangles of DNA within a cell's nucleus so that genetic information can be "read" and used to direct the synthesis of proteins, which have many specific functions in the body. More DNA Current Events and DNA News Articles |
|||||||||||||||||||||
|
|||||||||||||||||||||
|
|||||||||||||||||||||