 |
Landmarks in the
history of gene technology
|
| 1868 |
F.
Miescher, Switzerland, first isolates nucleic
acid from biological material. |
| 1940 |
G.
Beadle* and E.
Tatum, USA, put forward the "one gene
– one enzyme" hypothesis. (*1958) |
| 1944 |
O.
Avery, USA, shows that genetic material does
not consist of proteins but of deoxyribonucleic
acid (DNA). |
| 1953 |
J.
Watson*, USA, and F.
Crick*, UK, show that the DNA molecule
consists of a double helix, thus making one of
the most important discoveries of this century.
(*1962) |
| 1956 |
A.
Kornberg*, USA, discovers the enzyme DNA
polymerase, which is needed for copying DNA.
(*1959) |
| 1957 |
A.
Todd*, UK, receives the Nobel Prize in
Chemistry for synthesis DNA's building blocks.
Later G.
Khorana and his coworkers in the USA
develop these chemical methods further and, for
the first time (1970), synthesise a biologically
active gene. |
| 1961-65 |
Work by
M.
Nirenberg*, J. Matthei,
G.
Khorana*, S.
Ochoa and their co-workers in the USA
leads to an understanding of the genetic code.
(*1969) |
| 1961-69 |
W.
Arber*, Switzerland, D.
Nathans* and H.
Smith*, USA, discover restriction
enzymes, which can cleave DNA molecules in a
predetermined way and can hence function as
important tools in gene technology. (*1978) |
| 1972 |
P.
Berg*, USA, lays the foundation of
recombinant-DNA technology. (*1980) |
| 1975-77 |
W.
Gilbert*, USA, and F.
Sanger*, UK, develop methods for
determining the sequence of DNA. (*1980) |
| 1978 |
Michael
Smith*, Canada, and his co-workers manage to
induce a site-directed mutation in a
bacteriophage DNA molecule. |
| 1982 |
Michael
Smith* together with A. Fehrst and
G. Winter, UK, manages to produce large
quantities of an enzyme in which, using
site-directed mutagenesis, one pre-determined
amino acid is exchanged for another. (*1993) |
| 1985 |
The PCR method
developed by Kary B. Mullis*, USA, for
mass-copying of DNA is presented for the first
time. (*1993) |
| |
*Nobel
Prize |
|
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