1) scientists HAVE been experimenting with growing human parts on other species
2) animals used in genetic experimentation and xenotansplantation are not treated humanely
3) genetic modification goes outside the boundaries or normal species replication; there is no requirement that species be closely related for them to be hybidized in this way; once in a living organsim DNA mutates. Scientits have found that the GMO has more differences from the original donor species than just the modified genes.
4) once in the public market place (as with the tropical fish below) how do you propose to enforce controls keeping the GMO separate from the pure species?
http://education.guardian.co.uk/higher/research/story/0,,1177023,00.htmlHuman breasts grown on mice
Thursday March 25, 2004
The Guardian
Scientists who famously grew a human ear on the back of a mouse may finally have been trumped. Genetically engineered mice have now been used to grow lumps of human breast.
http://www.guardian.co.uk/life/thisweek/story/0,,1093632,00.htmlHow soon before we see GM pets in the shops?
Ian Sample
Thursday November 27, 2003
The Guardian
In January, American pet shops will begin stocking genetically modified versions of tropical freshwater zebrafish. The small fish, which are normally black and silver, have had the equivalent of a new paint job, thanks to the insertion of a gene extracted from sea anemones that makes them fluoresce bright red. It will be the first time GM pets have been available to the American public.
The new "GloFish" (above) were developed by scientists in Singapore to fluoresce only when they swam into polluted waters, turning them into living environmental monitors. But Yorktown Technologies, the Texas-based biotech company that is going to sell the fish, hopes they will make attractive pets, too.
http://education.guardian.co.uk/egweekly/story/0,,1081922,00.htmlMPs urge inquiry into Huntingdon xenotransplantation
Polly Curtis
Tuesday November 11, 2003
The Guardian
A committee of MPs is considering an investigation of the Home Office's animal research watchdog after it defended its decision to allow experiments involving the transplantation of genetically modified piglets' hearts into the necks of wild baboons to be classed as "moderate".
The xenotransplantation experiments were carried out before 2000 by private company Imutran at the Huntingdon Life Sciences laboratories in Cambridge. But details became public only after a legal battle between the company and animal rights group Uncaged Campaigns, to whom documents had been leaked. These documents, published in April, showed a quarter of the baboons died from "technical failures"; others were left with wounds weeping fluid and several died on the journey to Britain.
http://education.guardian.co.uk/higher/news/story/0,,845642,00.htmlControversy over 'new life' experiment
Staff and agencies
Friday November 22, 2002
A controversial American experiment to create new life forms could take place in the UK without public debate, a biotech watchdog warned today.
The caution from GeneWatch UK comes after US scientists announced they planned to engineer a single-celled man-made organism with the minimum number of genes necessary to sustain life. The project, funded by a £2m grant from the US energy department, has sparked an ethical debate about whether humans have the moral right to create new organisms
http://www.guardian.co.uk/genes/article/0,,627789,00.htmlDolly's arthritis
Friday January 4, 2002
Why does it matter that a sheep has arthritis?
Because the sheep in question, Dolly, was the world's first mammal cloned from an adult cell. If she is found to be prematurely aging it means that the cloning process may create genetic defects. Arthritis is an inflammation of the joints found most often in the elderly.
Why was Dolly cloned?
To see if cloning technologies could work. If they did, it would then be possible not just to make identical copies of animals (in itself relatively pointless) but to create animals genetically modified so that their internal organs could be transplanted to sick humans.
Are animal to human transplants now more or less likely?
It is difficult to say. PPL Therapeutics, the firm that helped to clone Dolly, this week announced it had cloned five piglets lacking an alpha gal gene. This, the company said, would be the first step towards creating "knock out pigs" that had their internal organs' natural resistance to be being put into humans made inactive.
But if Dolly was born with genetic defects leading to premature aging, the future of cloning becomes less certain. Its critics point out that many cloned animals die before birth or shortly after, often with genetic mutations. Putting a cloned animal organ that is genetically defective into a human being may not be as effective as it was once believed it could be, especially when the much longer lifespan of human beings than most farmyard animals is taken into account.