The History of DNA DiscoveryHere is the timeline of DNA Discovery
The History of DNA Discovery
On 25 April 1953, James Watson and Francis Crick, then at Cambridge University, reported the discovery of the structure of DNA (deoxyribonucleic acid) – the molecule that genes are made of.
Crick and Watson used model building to reveal the now famous double helix of DNA, but the X-ray crystallographic data of Rosalind Franklin and Maurice Wilkins at King’s College, London, were crucial to the discovery.
The DNA saga began in 1869, when Swiss biochemist Friedrich Miescher isolated a new substance from the nuclei of white blood cells. Researchers were recently aware that cells were the basic unit of life and Miescher was interested in their chemical components. Each morning, he called at the local clinic to pick up dirty bandages, for in the days before antiseptics these were soaked in pus – a good source of white blood cells with their large nuclei. Adding alkali made the cell nuclei burst open, releasing their contents, from which Miescher extracted DNA (which he called nuclein).
Analysis of this nuclein showed that it was an acid, containing phosphorus, so it did not fit into any of the known groups of biological molecules, such as carbohydrates and proteins. Nuclein was rechristened nucleic acid and, despite its chemical novelty, its biological significance was not fully realised for many more decades.
In 1879 the German biologist Walther Flemming discovered tiny thread-like structures called chromatin (later known as chromosomes) within the nucleus – so-called because they readily absorbed colour from the new stains used to reveal cellular components. Studies on cell division were to reveal the key role played by chromosomes in inheritance – how they double up before the cell splits, and then divide into two sets, taking a fresh copy into each ‘daughter’ cell.
Further analysis suggested that chromosomes contained DNA, which led another German researcher, Oskar Hertwig, to declare that ‘nuclein is the substance which is responsible … for the transmission of hereditary characteristics’.
By 1900, it was known that the basic building blocks of DNA were phosphate, a sugar (later shown to be deoxyribose) and four heterocyclic bases – two of which were purines [adenine (A) and guanine (G)] while the other two were pyrimidines [cytosine (C) and thymine (T)].
It was Phoebus Levene, of the Rockefeller Institute, New York, and a former student of the Russian chemist and composer Alexander Borodin, who showed that the components of DNA were linked in the order phosphate- sugar-base. He called each of these units a nucleotide, arguing that the DNA molecule consisted of a string of nucleotide units linked together through the phosphate groups, which are the ‘backbone’ of the molecule.
Levene was also convinced that the amounts of the four bases were the same in all DNA molecules, whatever their origin. So even when Swedish researchers Torbjörn Caspersson and Einar Hammersten showed, in the 1930s, that DNA was a polymer, most people continued to believe in Levene’s ‘tetranucleotide hypothesis’.
A breakthrough came from Oswald Avery, Colin McLeod and Maclyn McCarty, a team of medical microbiologists at the Rockefeller Institute in New York. They were trying to identify the nature of the ‘transforming principle’ – a substance discovered by English microbiologist, Fred Griffith, in 1928. Griffith had been experimenting with two species of pneumococcus, the bacteria that cause pneumonia.
Avery and his team showed by a process of elimination that DNA, not protein, was the transforming principle.
The final phase of solving the puzzle of the DNA structure relied on X-ray crystallography. The use of X-rays to solve the structures of large biological molecules began with Dorothy Hodgkin’s work on penicillin, lysosyme, and vitamin B12, and Max Perutz’s work on haemoglobin from the 1930s. By 1938, William Astbury, a student of William Bragg (who, with son Lawrence, had invented the technique in 1913) had X-ray pictures of DNA, but they were hard to interpret.
The late 1940s saw three separate groups working intensively on the DNA structure. At King’s College, London, Maurice Wilkins was intrigued by the long fibres that DNA forms when it is pulled out of watery solutions with a glass rod, wondering if this meant there was some regularity to its structure. 1951, Wilkins was joined by Rosalind Franklin, a British physical chemist who already had an international reputation for her work on the X-ray crystallography of coals. She set about building a dedicated X-ray lab at King’s and was soon producing the best images ever of DNA. These led her to the idea that maybe the DNA molecule was coiled into a helical shape.
Linus Pauling, the US chemist, and author of The nature of the chemical bond, began to think along similar lines. After all, Pauling had already discovered helical motifs in protein structures. Around this time, Francis Crick – with a background in maths and physics, and the younger James Watson, with expertise in the molecular biology of phage (viruses that infect bacteria, then used as a laboratory tool for genetic studies), joined forces at the Cavendish Laboratory in Cambridge, intent on cracking the DNA structure themselves, using a model building approach.
A seminal moment came when Wilkins showed Watson one of Franklin’s photos of the so-called B form of DNA. Previous studies had used the A form, which contains less water and had led to images that were hard to analyse. This picture, by contrast, was beautifully simple and seemed to point clearly to a helical structure for the molecule. As Watson puts it in his memoir: ‘The instant I saw the picture, my mouth fell open and my heart began to race’.
Model building – using metal plates for the nucleotides and rods for the bonds between them – now began in earnest. But Crick and Watson did not know whether to build their helix with the phosphates inside or outside, and they were unsure how to incorporate Chargaff’s ideas on base pairing.
The final clue came from another visitor to the Cavendish, the American chemist Jerry Donohue, who pointed out how hydrogen bonding allows A to bond to T and C to G. This allows a double helical structure for DNA, where the two strands have the bases on the inside, paired up, and the phosphates on the outside.
The true beauty of the model that Crick and Watson built was that the structure immediately suggested function. As they hinted, in their Nature paper: ‘It has not escaped our notice that the specific pairing we have postulated suggests a possible copying mechanism for the genetic material’.
The DNA molecule is self-replicating (as was proved by experiments a few years later) because it can unwind into two single strands. Each base then attracts its complementary base, by hydrogen bonding, so that two new double helices are assembled.
Franklin and Wilkins did not completely miss out on credit for the DNA structure; their own separate papers were published back to back with Crick and Watson’s in the same issue of Nature. Crick, Watson and Wilkins went on to win the Nobel Prize for their work in 1962.
The discovery of the DNA structure was the start of a new era in biology, leading, over the next two decades, to the cracking of the genetic code and the realisation that DNA directs the synthesis of proteins. There were technical advances too, such as DNA sequencing, genetic engineering, and gene cloning.
More recently, the complete sequences of many organisms have been solved – including the human genome in June 2000. The next 50 years of the DNA testing story will be all about realising the practical benefits of Crick and Watson’s discovery for humanity – in industry, medicine, food and agriculture.