
Professor John Shine
Professor John Shine AC FRS FAA was the Garvan Institute of Medical Research'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 developed the 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, CalBio 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 upon joining Garvan, with the DNA cloning of neuropeptide receptor subtypes.
Awards
- 2017
Companion - General Division of the Order of Australia
- 2010
Prime Ministers Prize for Science
- 1996
Officer - General Division of the Order of Australia
- 1994
Fellow - Australian Academy of Science
- 1982
Gottschalk Medal - Australian Academy of Science
- 1980
Boehringer-Mannheim Medal - Australian Biochemical Society
Selected publications
See all publications- PUBLISHED 26 September 2025European Journal of Human Genetics : EJHG
PKD1 5'UTR variants are a rare cause of disease in ADPKD and suggest a new focus for therapeutic development
- PUBLISHED 19 December 2024NPJ Genomic Medicine
Somatic mutation in autosomal dominant polycystic kidney disease revealed by deep sequencing human kidney cysts
- PUBLISHED 7 July 2023NPJ Genomic Medicine
Atypical splicing variants in PKD1 explain most undiagnosed typical familial ADPKD
- PUBLISHED 12 January 2021European Journal of Human Genetics : EJHG
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing
- PUBLISHED 29 October 2018Genetics in Medicine : Official Journal of the American College of Medical Genetics
Population data improves variant interpretation in autosomal dominant polycystic kidney disease
