3 scientists win Nobel in medicine

AS a child in Italy during World War II, he lived for years on the streets and in orphanages.

Six decades later, as a scientist in the United States, Mario Capecchi joined two other researchers in winning the Nobel Prize in medicine. Their work led to a powerful and widely used technique to manipulate genes in mice, which has helped scientists study heart disease, diabetes, cancer, cystic fibrosis and other diseases.The US$1,54 million prize was awarded on Monday to Capecchi (70) of the University of Utah in Salt Lake City; Oliver Smithies (82), a native of Britain now at University of North Carolina in Chapel Hill, and Sir Martin J Evans (66) of Cardiff University in Wales.Their “gene-targeting” technique lets scientists deactivate or modifying individual genes in mice and observe how those changes affect the animals.That in turn gives clues about what those genes do in human health and disease.The work has had “a revolutionary effect on the ability to understand how genes work”, said Richard Woychik, director of The Jackson Laboratory in Bar Harbour, Maine, a centre for mouse genetics.The prize is a particularly striking accomplishment for Capecchi.A native of Italy, he was separated from his mother at age 3 when the Gestapo took her to the Dachau concentration camp as a political prisoner in 1941.His mother, a poet, and his father, an Italian military officer, were not married.Capecchi spent a year with a peasant family, until the money his mother left for his care ran out.At age 4, “I started wandering the streets,” he recalled on Monday.For about four years, he lived on the streets or in orphanages, and he ended up in a hospital with malnutrition.Dachau was liberated in 1945 and his mother survived.”Then she set out to find me,” searching through hospital records.”I was in a hospital and when they keep you in a hospital, they didn’t want you to run around.They took your clothes away.She came and bought me an outfit.”She showed up on Capecchi’s 9th birthday.Soon thereafter, “we were on a boat to America …I literally expected roads to be paved with gold.What I found was, it was a land of opportunity”, he said.In the United States, he went to school for the first time, starting in third grade despite not knowing English.The three prize-winning scientists mostly worked separately, although they exchanged information about their research.Evans identified embryonic stem cells in mice, while the gene-targeting technique used on those cells came from work by Capecchi and Smithies.Capecchi’s work has uncovered the roles of genes involved in organ development in mammals, the committee said.Evans developed strains of gene-altered mice to study cystic fibrosis, and Smithies created strains to study such conditions as high blood pressure and heart disease.To create gene-altered mice, researchers introduce a genetic change into mouse embryonic stem cells.These cells are then injected into mouse embryos.The mice born from these embryos are bred to produce offspring with the changed genes.In 1989, the first mice born with genes manipulated through the technique was announced.More than 10 000 different genes in mice have since been studied this way, the Nobel committee said.That’s about half the genes the rodents have.Apart from making mice with altered DNA, the work has also shown how to manipulate genes in human embryonic stem cells for lab research.Such basic studies can help scientists learn how to turn the cells into specialised cells that might prove useful in therapy, said Doug Melton, co-director of the Harvard Stem Cell Institute.And scientists hope that by putting disease-related genes into human embryonic cells for lab studies, they can learn how the diseases develop and screen potential therapies, said John Gearhart, a stem cell expert at the Johns Hopkins School of Medicine.The prize-winning work has “formed the foundation for much of what we do” in human embryonic stem cell research, Melton said.The medicine prize was the first of six Nobel awards to be announced.The others are chemistry, physics, literature, peace and economics.Nampa-APTheir work led to a powerful and widely used technique to manipulate genes in mice, which has helped scientists study heart disease, diabetes, cancer, cystic fibrosis and other diseases.The US$1,54 million prize was awarded on Monday to Capecchi (70) of the University of Utah in Salt Lake City; Oliver Smithies (82), a native of Britain now at University of North Carolina in Chapel Hill, and Sir Martin J Evans (66) of Cardiff University in Wales.Their “gene-targeting” technique lets scientists deactivate or modifying individual genes in mice and observe how those changes affect the animals.That in turn gives clues about what those genes do in human health and disease.The work has had “a revolutionary effect on the ability to understand how genes work”, said Richard Woychik, director of The Jackson Laboratory in Bar Harbour, Maine, a centre for mouse genetics.The prize is a particularly striking accomplishment for Capecchi.A native of Italy, he was separated from his mother at age 3 when the Gestapo took her to the Dachau concentration camp as a political prisoner in 1941.His mother, a poet, and his father, an Italian military officer, were not married.Capecchi spent a year with a peasant family, until the money his mother left for his care ran out.At age 4, “I started wandering the streets,” he recalled on Monday.For about four years, he lived on the streets or in orphanages, and he ended up in a hospital with malnutrition.Dachau was liberated in 1945 and his mother survived.”Then she set out to find me,” searching through hospital records.”I was in a hospital and when they keep you in a hospital, they didn’t want you to run around.They took your clothes away.She came and bought me an outfit.”She showed up on Capecchi’s 9th birthday.Soon thereafter, “we were on a boat to America …I literally expected roads to be paved with gold.What I found was, it was a land of opportunity”, he said.In the United States, he went to school for the first time, starting in third grade despite not knowing English.The three prize-winning scientists mostly worked separately, although they exchanged information about their research.Evans identified embryonic stem cells in mice, while the gene-targeting technique used on those cells came from work by Capecchi and Smithies.Capecchi’s work has uncovered the roles of genes involved in organ development in mammals, the committee said.Evans developed strains of gene-altered mice to study cystic fibrosis, and Smithies created strains to study such conditions as high blood pressure and heart disease.To create gene-altered mice, researchers introduce a genetic change into mouse embryonic stem cells.These cells are then injected into mouse embryos.The mice born from these embryos are bred to produce offspring with the changed genes.In 1989, the first mice born with genes manipulated through the technique was announced.More than 10 000 different genes in mice have since been studied this way, the Nobel committee said.That’s about half the genes the rodents have.Apart from making mice with altered DNA, the work has also shown how to manipulate genes in human embryonic stem cells for lab research.Such basic studies can help scientists learn how to turn the cells into specialised cells that might prove useful in therapy, said Doug Melton, co-director of the Harvard Stem Cell Institute.And scientists hope that by putting disease-related genes into human embryonic cells for lab studies, they can learn how the diseases develop and screen potential therapies, said John Gearhart, a stem cell expert at the Johns Hopkins School of Medicine.The prize-winning work has “formed the foundation for much of what we do” in human embryonic stem cell research, Melton said.The medicine prize was the first of six Nobel awards to be announced.The others are chemistry, physics, literature, peace and economics.Nampa-AP