Dolly and her surrogate mother
Dolly was part of a series of experiments at The Roslin Institute that were trying to develop a better method for producing genetically modified livestock. If successful, this would mean fewer animals would need to be used in future experiments. Scientists at Roslin also wanted to learn more about how cells change during development and whether a specialised cell, such as a skin or brain cell, could be used to make a whole new animal.
These experiments were carried out at The Roslin Institute by a team led by Professor Sir Ian Wilmut. Because of the nature of the research, the team was made up of many different people, including scientists, embryologists, surgeons, vets and farm staff.
Dolly was cloned from a cell taken from the mammary gland of a six-year-old Finn Dorset sheep and an egg cell taken from a Scottish Blackface sheep. She was born to her Scottish Blackface surrogate mother on 5th July 1996. Dolly’s white face was one of the first signs that she was a clone because if she was genetically related to her surrogate mother, she would have had a black face.
Because Dolly’s DNA came from a mammary gland cell, she was named after the country singer Dolly Parton.
Learn more about cloning with our cloning FAQs.
Why was Dolly so important?
Dolly was important because she was the first mammal to be cloned from an adult cell. Her birth proved that specialised cells could be used to create an exact copy of the animal they came from. This knowledge changed what scientists thought was possible and opened up a lot of possibilities in biology and medicine, including the development of personalised stem cells known as iPS cells.
However, Dolly was not the first ever cloned mammal. That honour belongs to another sheep which was cloned from an embryo cell and born in 1984 in Cambridge, UK. Two other sheep, Megan and Morag, had also been cloned from embryonic cells grown in the lab at The Roslin Institute in 1995 and six other sheep, cloned from embryonic and foetal cells, were born at Roslin at the same time as Dolly. What made Dolly so special was that she had been made from an adult cell, which no-one at the time thought was possible.
Dolly was announced to the world on 22nd February 1997 to a frenzy of media attention. The Roslin team chose to make the announcement at this time to coincide with the publication of the scientific paper which describes the experiments that produced her. Dolly captured the public’s imagination – no small feat for a sheep – and sparked a public debate about the possible benefits and dangers of cloning.
Dolly meets the world’s media. Image copyright: Murdo Macleod
In the week following the announcement, The Roslin Institute received 3,000 phone calls from around the world.
When Dolly was one year old, analysis of her DNA showed that her telomeres were shorter than would be expected for a normal sheep of the same age. Telomeres are ‘caps’ on the ends of DNA molecules that protect the DNA from damage. As an animal or person ages, their telomeres become progressively shorter, exposing the DNA to more damage.
It’s thought that Dolly had shorter telomeres were because her DNA came from an adult sheep and the telomeres had not been fully renewed during her development. This could have meant that Dolly was ‘older’ than her actual age. However, extensive health screens on Dolly at the time did not find any conditions which could be directly related to premature or accelerated ageing.
Dolly and Bonnie
Dolly spent her life at The Roslin Institute and, apart from the occasional media appearance, led a normal life with the other sheep at the Institute. Over the years Dolly had a total of six lambs with a Welsh Mountain ram called David. Their first lamb, Bonnie, was born in April 1998, twins Sally and Rosie were born the following year and triplets Lucy, Darcy and Cotton the year after.
After Dolly gave birth to her last lambs in September 2000, it was discovered that she had become infected by a virus called Jaagsiekte sheep retrovirus (JSRV), which causes lung cancer in sheep. Other sheep at The Roslin Institute had also been infected with JSRV in the same outbreak.
In 2001, Dolly was diagnosed with arthritis after farm staff noticed her walking stiffly. This was successfully treated with anti-inflammatory medication, although the cause of the arthritis was never discovered.
Dolly continued to have a normal quality of life until February 2003, when she developed a cough. A CT scan showed tumours growing in her lungs and the decision was made to euthanise Dolly rather than risk her suffering. Dolly was put to sleep on 14th February 2003, at the age of six.
Where is Dolly now?
After her death The Roslin Institute donated Dolly’s body to the National Museum of Scotland in Edinburgh, where she has become one of the museum’s most popular exhibits. Dolly is back on display in the museum after an extensive gallery refurbishment, alongside an interactive exhibit on the ethics of creating transgenic animals featuring current research from The Roslin Institute.
National Museums Scotland blog post – ‘Goodbye Dolly’
Essay on Ian Wilmut and the Cloning of Dolly
4070 Words17 Pages
Ian Wilmut and the Cloning of Dolly
Definitions of creativity vary based on different people’s interpretations, yet most people agree that creative individuals produce new ideas that can completely change or invent a domain. According to Howard Gardner, creativity is not limited to a single domain, but is unique for all seven domains. Creativity is based on three core elements: the relationship between the child and the master, the relationship between an individual and the work in which he/she is engaged, and the relationship between the individual and others, such as family and friends (Gardner, 9). I believe that Ian Wilmut is a creative master in the logical mathematical domain because in July 1996, he completely changed his…show more content…
“To get a cell from an adult mammal to behave like a cell from a developing embryo had long since been abandoned at major centers of scientific research” (Healy, 176). The doubt of others didn’t sway Wilmut’s ideas. He used a method called somatic cell nuclear transfer cloning in order to produce Dolly. This same technique has now been used for application of human stem cells to generate differentiated tissues (and this same technique could also be used to clone a human from an adult cell). Click on this animation on somatic cell nuclear transfer. Wilmut first took a nucleus from the mammary cells of a dead six-year-old Finn Dorset Sheep. He then substituted the nucleus for the nucleus of an egg from a different sheep- a Poll Dorset. Next, Wilmut implanted the egg into an ewe of a Scottish Blackface who became Dolly’s surrogate mother. Five months later, Dolly was born (Wills, 22). Wilmut used three different breeds of sheep so it would be apparent that Dolly’s genes did not come from her surrogate mother nor the egg donor, but from the six year old, Finn Dorset. In addition, in order to account for problems such as cells being in the wrong stage, or having the wrong set of genes turned on, or having cells that are too metabolically active, Wilmut starved the cells for several days. He then fused the starved cell with enucleated eggs. This made the DNA copying device in the cell to stop by “arresting the cell cycle and forcing the cells into