Prof John Shine
John Shine was Garvan's Executive Director from 1990-2011. His name is known to most undergraduate biology students for his role in defining the Shine-Dalgarno gene sequence, which is responsible for the initiation and termination of protein-synthesis.
John has a number of other significant scientific ‘firsts’ under his belt. He was a central figure in the cloning of the insulin and growth hormone genes; was the first to clone a human hormone gene; was responsible for cloning of an endorphin gene and was the first to demonstrate that hormone genes cloned in bacteria could be expressed in a biologically active form. He also determined the first sequence responsible for replication of a cancer-causing virus.
John’s scientific career took off following a move, in 1975, to San Francisco. It was there that he cloned numerous genes as well as develop techniques to do this – he is a sole inventor on a patent for using phosphatase to direct the joining of DNA molecules.
A three year appointment at California Biotechnology (CalBio) Inc company saw John guide it from a staff of some 15 scientists in 1984 to over 200 in 1987. During this period, Cal Bio developed several important new therapeutics including treatments for congestive heart failure, infant respiratory distress syndrome, and burns and general wound healing agents. At the same time, John developed an interest in the generation of functional diversity in the nervous system, a research area he established on joining the Garvan.
In the News2016 Shine Translational Research Fellowship awarded - May 21, 2016
Professor John Shine named an Honorary Fellow of AAHMS - Oct 12, 2015
NHMRC Recognises John Mattick, John Shine and Peter Wills - Jan 14, 2014
Professor John Shine wins Peter Wills Medal - Dec 05, 2011
Garvan announces appointment of next Executive Director - Sep 05, 2011
Rally for Research (Sydney) - Apr 15, 2011
Rumoured NHMRC cuts would cripple medical research sector - Apr 08, 2011
Professor John Shine wins 2010 Prime Minister’s Prize for Science - Nov 18, 2010
DA Approval for Major Australian Cancer Centre - Jan 19, 2010
Garvan St Vincent’s Campus Cancer Centre Welcomes $70 million from Federal Government - May 14, 2009
Shining bright: Twenty years at Garvan - Jun 22, 2007
Awards and Honours
1982 - Gottschalk Medal, Australian Academy of Science
1994 - Fellow, Australian Academy of Science
1996 - Officer, General Division of the Order of Australia
2010 - Prime Ministers Prize for Science
1975 - PhD, Australian National University
2006 - DSc (Honoris causa), University of New South Wales - Australia
Herzog H, Hort YJ, Ball HJ, Hayes G, Shine J, Selbie LA. Cloned human neuropeptide Y receptor couples to two different second messenger systems. P Natl Acad Sci, USA 1992; 89:5794-5798.
Evans HF, Shine J. Human galanin: molecular cloning reveals a unique structure. Endocrinology 1991; 129:1682-1684.
Greene GL, Gilna P, Waterfield M, Baker A, Hort Y, Shine J. Sequence and expression of human estrogen receptor complementary DNA. Science 1986; 231: 1150-1154
Shine J, Fettes I, Lan NC, Roberts JL, Baxter JD. Expression of cloned b-endorphin gene sequences by E. coli. Nature 1980; 285: 456-461
Seeburg PH, Shine J, Martial JA, Ivarie RD, Morris JA, Ullrich A, Baxter JD, Goodman HM. Synthesis of growth hormone by bacteria. Nature 1978; 276: 795-798
Shine J, Seeburg PH, Martial JA, Baxter JD, Goodman HM. Construction and analysis of recombinant DNA for human chorionic somatomammotropin. Nature 1977; 270: 494-499
Ullrich A, Shine J, Chirgwin J, Pictet R, Tischer E, Rutter WJ, Goodman HM. Rat insulin genes: construction of plasmids containing the coding sequences. Science 1977; 196: 1313-1319
Shine J, Dalgarno L. Determinant of cistron specificity in bacterial ribosomes. Nature 1975; 254 34-38
Shine J, Dalgarno L. The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites. Proc Natl Acad Sci USA 1974; 71: 1342-1346
Dalgarno L, Shine J. Conserved terminal sequence in 18S rRNA may represent terminator anticodons.Nature New Biology 1973; 245: 261-262