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    What is DNA?
   DNA timeline
    Discovery of the double helix
    Why a double helix?

Explaining DNA

DNA timeline

1865   Gregor Mendel, working alone in an Austrian monastery, discovers that some characteristics are inherited in ‘units’.
1870   Friedrich Miescher isolates chemicals from the cell nucleus, including ‘nucleic acids’. However, most people are more interested in proteins in the nucleus.
1879   Walter Flemming describes behavior of chromosomes during cell division, implicating these nuclear structures in inheritance.
1900   Hugo DeVries and others rediscover Mendel’s work and establish first laws of inheritance.
1909   Wilhelm Johannsen coins the term ‘gene’.
1911   Thomas Hunt Morgan is the first to show that genes are arranged in a linear fashion along chromosomes.
1928   Frederick Griffith uses a chemical extract to convert harmless pneumonia bacteria into pathogenic forms. The nature of this ‘inheritance factor’, however, is unknown.
1929   Phoebus Levene discovers that a sugar, deoxyribose, is present in nucleic acids. Later identifies that DNA is made up of nucleotides, a chemical unit comprising a deoxyribose sugar, a phosphate group and one of four small organic molecules known as bases.
1941   George Beadle and Edward Tatum show that genes direct the production of proteins.
1943   William Astbury makes the first X-ray diffraction images of DNA.
1944   Building on Griffith’s work, Oswald Avery and colleagues show that DNA can ‘transform’ cells, cementing the link between DNA and genes.
1950   Edwin Chargaff discovers that there are patterns in the amounts of the four bases in DNA: the amounts of G and C, and of A and T, are always the same.
1951   Rosalind Franklin takes her first X-ray diffraction pictures.
1953  

James Watson and Francis Crick publish first paper proposing a double helix structure for DNA.
Isaac Newton: “If I have seen further it is by standing on the shoulders of giants.”