[Music] Devon and SKy Cooper are brother and sister both of them have CLE cell anemia before the Advent of modern medicine CLE cell anemia almost certainly meant death before adulthood even today young patients can suffer strokes and organ failure CLE cell anemia is a genetic disease parents of those who have the disease might not have it themselves but both must carry the Sickle Cell character in their DNA so how's it going good can I see your hands this is pretty where did that come from was that from Brooklyn besides some bone pain Sky leads the Fairly normal life of a 13-year-old girl but her younger brother Devon has suffered acute chest syndrome and has already had his spleen removed so you don't get any more belly pains that's good sky and Devon symptoms arise from the fact that some of their red blood cells become misshapen crescents instead of discs preventing enough oxygen from being delivered to all parts of the body it's not completely clear why symptoms are variable but what is most perplexing about CLE cell disease is that it's not rare So in the United States we think there are between 70 and 125,000 persons with CLE cell disease um however that doesn't take into account immigration and other uh patients or persons coming from other parts of the world into the country in fact in some populations African-Americans for example the incidence is as high as 1 in 500 astoundingly high for a deadly inherited disease didn't Darwin teach us that harmful traits disappear from the gene pool through natural selection why is sickle cell anemia so prevalent and why in particular among people of African descent [Music] the answers to these questions began with a remarkable set of observations from an unlikely person more than 60 years [Music] ago Tony Allison has spent most of his career as a medical doctor and molecular biologist in the US and England but he grew up in e Africa and he's quick to recall his formative years in Kenya point is that we lived in in the up country and we used to go to the coast every year in August for the holiday when it was a little bit cooler than at other times so we had the trip all the way down which was usually with a truck and a car and uh so we would camp on the way in in Sao and there would be lions roaring around so it was really quite exciting these are the infamous Sao lions INF from our minds around 1950 biologists didn't know a lot about the details of evolution because we didn't know really how heredity worked the structure of DNA had not been discovered yet genetic code had not been cracked so we know that while Evolution was due to genetic changes uh we didn't know how those genetic changes took place whatsoever so there were holes in the whole picture of the evolutionary process and Tony Allison was probably the least likely person you would imagine who would fill one of the most critical holes he grew up far away from the centers of Science in Europe and North America he was really interested in natural history and he loved the Kenyan wildlife and he visited archaeological digs that were going on at the time but it was a really circuitous and serendipitous route that led him to an enormous discovery in evolutionary biology Tony first went to University in South Africa where he studied physical anthropology then to medical school at Oxford he had a deep interest in human Origins but not so much in ancient stones and Bones Tony was interested in blood could the common blood types say anything about the evolutionary history of East African tribal people and I actually learned just before going out about the Sickle Cell condition nobody really knew the frequencies of CLE cells in East Africa so it was a a baron slate so to speak blood samples from people carrying the CLE cell character appear quite normal until oxygen is removed Tony learned that adding a chemical agent to the samples would quickly reduce oxygen and reveal CLE cells if they were there this gave him an easy test to score blood samples for the CLE cell character what was striking was that you had high frequencies of people carrying the Sickle Cell character right in the coast and near Lake Victoria and very low frequencies in the High Country in between in Nairobi what could possibly account for such a striking disparity the CLE cell character was understood to be genetic not environmental Tony had grown up in the dry Kenyon Highlands but he knew the warm moist lanss were a breeding ground for the anopheles mosquito that carried the malaria parasite plasmodium ferin and it dawned on them the places where there was a really high incitive CLE cell was where there was a really high incidence of malaria bang now it was a burning question that confronted Tony could sickle cell and malaria be connected and if so how it would it was a radical notion that a genetic disease could somehow be connected to an infection when you went back to Oxford you had this idea of a linkage between CLE cell and malaria you hadn't published it did you know it was a big deal I mean did you I sure it was a big deal was a big deal so you were but that's why that's why I wanted not to go off half cocked yeah I wanted to have a really complete story so he decided he had to sit on this idea until he got a chance to test it properly so and a key element of the scientific method is to come up with a hypothesis that's great but you've got to test it in every way possible to see whether or not it can hold up to that sort of scrutiny that's how science moves forward well the scientific method essentially means that you address a problem and try to find a solution so you look at Children of the appropriate age and find out whether they are in fact protected against Valaria and if that's the case you predict that you will have high frequencies of Sickle cells only in areas where malaria is endemic you wanted to know that this this correlation held not just in Kenya but everywhere it would be important to look directly at the incidence of malaria and CLE cell in as many areas as possible so Tony went on a Sickle Cell Safari he wanted to gather blood samples from all over East a Africa to really test this correlation and now he was a trained medical doc so he had something to offer so he would go into the market on Market day and offer to do checkups on children and just take a little finger prick or a little heel prick to get a sample of blood the first thing he did was look at the malaria parasite load in each sample then he tested for the Sickle Cell character he found that children carrying the character had a lower parasite count as if they were partially protected against malaria and when he examined the blood of about 5,000 individuals a really massive study the correlation was really clear so clear in fact that he could really draw a map of East Africa and shade in the areas of high incidence of sickle cell and they were superimposed right on top of the areas of high incidents of malaria bang that was it the many samples and detailed maps made it clear there was a connection between CLE cell and malaria but to understand how CLE cell might protect people from malaria required thinking about the genetics of CLE cell what happens is the genes are lined up on chromosomes and one has pairs of them with the exception of the sex chromosomes and this means that you have two copies so the copies can be the same or they can be different and if they the same they are called homozygous and if they're different they're called heterozygous when an individual finds a partner and reproduces one of each pair of chromosomes is passed on if the parents are both heterozygous carrying one sickle cell and one normal Gene odds are one in four that the child will be Sickle Cell homozygous two and four that the child will be heterozygous and one in four that the child will carry two copies of the normal Gene in the absence of malaria there is strong selection against the CLE cell Gene however in a malarial environment individuals born with two copies of the CLE cell Gene and those born with two copies of the normal Gene are both at a disadvantage one gets sickle cell disease the other is most vulnerable to malaria Tony's brilliant Insight was that those that carried just one CLE cell Gene had an innate resistance to malaria malaria tipped the selective balance in favor of heterozygotes the evolutionary trade-off is that protection from malaria comes at the cost of more CLE cell disease in the population the CLE cell mutation was not the best genetic solution you might imagine to resist malaria that's not how Evolution works it was the most available a simple typo a to to te in the gene that encodes hemoglobin mistakes are made in the copying of DNA in every generation you and I were born with about 40 or 50 mutations that didn't exist in either of our parents it's just part of the nature of copying three billion letters in the in the process of reproduction uh and when those mistakes arise a typo arises in the globin Gene for most of us that would be a bad thing but if you live in a malarial area it gives you an edge against the malarial parasite so that m is retained well Fitness essentially is a measure of whether a particular Gene is likely to be passed on to the next generation and this means that for that to happen the individual carrying that Gene has to survive to reproductive age and secondly has to reproduce now you had a sense that you had this explanation that was General to to the prevalence of CLE cell and it's and it's correlation with malaria but you didn't quite know the mechanism right so that's right what did you do next well I have to say I I left that part of the story to others because it's quite a complex Story I mean a large body of subsequent research has shown that the CLE cell mutation compromises the ability of the parasite to reproduce thus a mutation that creates one genetic disease can also protect against another disease what Tony gave us was a fully worked out example of evolution by natural selection and the amazing thing was this was in humans this is how natural selection was working on humans in real time in the real world Tony's map of East Africa was a stunning achievement but he could go further than that he knew that there was a high incidence of CLE cell in southern Europe in Southern India and in other parts of Africa and it turns out these are all malarial zones as well and so his map applied not just to East Africa but that whole part of the world well what I'm explaining about the origins of SLE cell disease and this association with malaria to children or their families they often look at me with incredulity they don't understand like you're kidding right this is all to do with the mosquito infection as our species has been able to move across the globe to areas with low malarial incidents this Gene is now really more of a nuisance than anything else it's not really a clear selective Advantage for them in Boston let's say um but it takes thousands of years for the population to change and for genetics to change based on the pressures around them in the environment what Tony Allison did first with his sharp intuition and then with his rigorous research will stand as a monument bringing our own evolutionary process into the light [Music]