Sydney Brenner (1927 - 2019) - MRC Laboratory of Molecular Biology (2024)

Sydney Brenner, Director of the LMB from 1979 to 1986 and 2002 Nobel Laureate, died on Friday 5thApril 2019, aged 92. From the 1950s, Sydney was at the forefront of many developments in molecular biology, in particular in molecular genetics, including the unravelling of the genetic code, and the discovery of messenger RNA. He initiated the work on the nematode worm, Caenorhabditis elegans, to study how genes regulate organ development and how cells are programmed to die. He was a key member of the LMB for 30 years, 20 of which he shared an office and ideas with Francis Crick.

Sydney was born in Germiston, South Africa on 13th January 1927. He attended Germiston High School and in 1942, at the age of 15, enrolled at the University of Witwatersrand, Johannesburg. He initially studied physics, chemistry, botany and zoology before moving to medical school, where courses in anatomy and physiology sparked his interest in cells and their function. Realising he would be too young to qualify to practise medicine at the end of his studies, he undertook a second B.Sc. (Hons.) in Anatomy and completed a M.Sc. in 1947. He then returned to medical studies and obtained a M.B. Bch. In 1952, he moved to the University of Oxford to undertake a PhD in the Physical Chemistry Laboratory under Sir Cyril Hinshelwood. He returned to South Africa in 1954 and became a lecturer at the Department of Physiology at Witwatersrand. There he developed an interest in solving the genetic code and he looked for a bacteriophage system that might help with this quest.

In 1956, Sydney returned to Britain and joined the MRC Unit for Research on the Molecular Structure of Biological Systems (now the LMB) in Cambridge, mainly due to the efforts of Francis Crick. Sydney joined Francis in the LMB’s Molecular Genetics Division (now the Cell Biology Division). During his first years in the Lab, Sydney continued his work on the genetic code, mutagenesis and the regulation of DNA replication.

His early work concentrated on the structure of bacteriophage and he showed that the particles were built of component parts. This work also resulted in the introduction, by Sydney and R W Horne, of negative staining as a method for high-resolution electron microscopy of biological objects. He also worked on acridine dye induced mutations, introducing the idea of frame shift mutations, and this provided the genetic evidence for the triplet code.Collaborating with Francois Jacob and Matthew Meselson, he provided the experimental evidence for messenger RNA, by showing that in phage infection pre-existing ribosomes were programmed by RNA newly synthesised from the viral DNA. Work on chain termination mutations provided proof of the colinearity of the gene with the polypeptide chain, which led to the definition and identification of the three chain terminating triplets, stop codons, and the demonstration that the phenomenon of suppression was due to mutations in transfer RNAs.With Francois Jacob he introduced the replicon model which provided the basis for understanding the replication of chromosomes and episomes in bacteria.

In 1962, Sydney initiated a research programme aimed at understanding the genetic basis of biological complexity. For the experimental work he chose the nematode worm, C. elegans, carrying out extensive research on the genetics, anatomy, development and molecular biology of this organism. Sydney worked out the methods of genetic analysis and in 1974 published an account of this research, which included the identification and mapping of about one hundred genes. He also began research on the complete three-dimensional reconstruction of the cellular anatomy of C. elegansfrom serial section electronmicrographs. In 1975, the first paper on the sensory nervous system of C. eleganswas published. This work, continued in collaboration with John White and Nicol Thomson, both at the LMB, resulted in the complete characterisation of the structure of C. elegans, in particular a detailed analysis of the nervous system and all neuronal connections. Another early collaborator in the project, John Sulston, also at the LMB, went on to complete the total analysis of the embryonic lineage of the organism so that the location of every cell and its origin in development was known. Sydney also recognised the need to establish a molecular approach to problems of development and began work on the genetics of muscle in C. elegans. This work culminated in the cloning and direct analysis of four genes specifying heavy chains of myosin. It led to the molecular genetic approach to problems of development and cellular function in C. elegans, and the project attracted a large number of talented young scientists to the LMB, who then went on to set-up their own laboratories. Sydney established C. elegansas an experimental model for the study of complex biological processes of multicellular organisms.C. elegansis still studied worldwide today and its use has led to breakthroughs in many areas of biological research. Sydney’s work on C.eleganswas awarded the 2002 Nobel Prize for Physiology and Medicine, which he shared with John Sulston and Bob Horvitz, for their discoveries concerning the genetic regulation of organ development and programmed cell death in C. elegans.

Sydney left the LMB in 1986 and set up the MRC Unit of Molecular Genetics, in Cambridge, and in 1995 he founded The Molecular Sciences Institute at La Jolla and Berkeley, USA and was both President and Director of Science.In 2000, he was appointed a Distinguished Professor in the Salk Institute, La Jolla, USA. Away from Cambridge, Sydney moved onto a new model organism, Fugu, the Japanese puffer fish, and he led the work on sequencing the Fugugenome, both at the Molecular Sciences Institute and the Institute of Molecular and Cell Biology in Singapore. In 1993, in Nature, Sydney and colleagues reported that the genome of Fugu rubripeswas the most compact vertebrate genome then known.

Away from the bench, Sydney undertook a number of roles, including Editor-in-Chief of the Journal of Molecular Biology, and he was known for his insightful and witty columns in Current Biology.He was a brilliant writer and storyteller.He was also involved in the 1975 Asilomar Conference, on the scientific opportunities and potential risks of new technology, such as recombinant DNA, at which his strong sense of ethical responsibility was a key motivator. In the early 1990s, he supported and encouraged Britain’s participation in the Human Genome Project. He was the founder of a number of biotechnology companies, including Compass Genetics and Population Genetics Technologies.

Sydney was known for his ferocious intelligence and wit, he was eager, high-spirited and creative. In science, he dazzled with his analysis and theories, but was also the master of the minimalist experiment. Francis Crick recalled, ‘his great strength was in experiments, and in particular the choice and execution of ones that were both important and ingenious’. Sydney had an extraordinary career, played a key role throughout the early days and development of molecular biology and is one of the greatest biologists of the 20thcentury. He has been a major influence to many scientists around the world and inspired many young scientists.

Sydney was joint Head of the LMB’s Cell Biology Division, with Francis, from 1963 and Head from 1977-1979. He was the second Director of the LMB, from 1979-1986, taking over from Max Perutz. Sydney became a member of EMBO in 1964, Fellow of the Royal Society in 1965 and Foreign Associate of the National Academy of Sciences in 1977. He was awarded the Companion of Honour in 1987.

Jan Löwe, LMB Director, said “with Sydney, biology is losing one of its true greats, a pioneer, a trailblazer and a shining example of the eternal LMB spirit. For example, one of his achievements, mapping the connectome of C. elegans neurons, is only now being recognised as the absolute starting point of the current journey to understand the brain in its entire complexity”.

Fiona Watt, Executive Chair MRC, added, “Sydney Brenner’s death marks the end of an era for the MRC. In 1956 he joined the forerunner of the Laboratory for Molecular Biology in Cambridge and he was LMB Director from 1979 to 1986. In addition to his major research discoveries his influence extended far beyond the lab. He inspired many young scientists and his curiosity and wit did not diminish with age. He will be sorely missed”.

Further References

LMB Nobel Page

Sydney Brenner (1927 - 2019) - MRC Laboratory of Molecular Biology (2024)

FAQs

What was Sydney Brenner experiment? ›

Brenner, Crick and their colleagues demonstrated, through mutations in E. coli, that the genetic code was made up of triplets of nucleotides (which Brenner named 'codons'). This research was followed by investigating the relationship of messenger RNA to DNA.

What did Sydney Brenner discover? ›

During his career, Sydney made several seminal discoveries including cracking the genetic code (Brenner 1957; Crick et al. 1961), codiscovering messenger RNA (Brenner et al. 1961), establishing the tiny roundworm Caenorhabditis elegans as a genetic model (Brenner 1974; White et al.

When did Sydney Brenner discover mRNA? ›

Sydney Brenner, Francois Jacob, and Matthew Meselson discovered that mRNA is the molecule that takes information from DNA in the nucleus to the protein-making machinery in the cytoplasm.

Why did Sydney Brenner choose C. elegans? ›

An important reason C. elegans was chosen for study was that high-quality electron micrographs had been obtained from specimens of this species by Nichol Thomson, who was hired by Brenner in October, 1964. Initially, Brenner began reconstructing the nervous system by hand.

What was the experiment on the genetic code? ›

The Nirenberg and Leder experiment was a scientific experiment performed in 1964 by Marshall W. Nirenberg and Philip Leder. The experiment elucidated the triplet nature of the genetic code and allowed the remaining ambiguous codons in the genetic code to be deciphered.

How was the genetic code deciphered? ›

The code was deciphered in two stages over a five-year period between 1961 and 1966. During the first stage, the base compositions of codons were deciphered by the directing cell-free protein synthesis with randomly ordered RNA preparations.

What was the Crick and Brenner experiment? ›

In 1961, Crick, Barnett, Brenner, and Watts-Tobin (Crick et al., 1961) designed an elegant experimental strategy to determine the nature of the genetic code. Remarkably, they reached the correct conclusion despite the absence of technology to analyze and compare DNA and protein sequences.

Where did Sydney Brenner go to college? ›

His father, a cobbler, came to South Africa from Lithuania in 1910, and his mother from Riga, Latvia, in 1922. He had one sister, Phyllis. He was educated at Germiston High School and the University of the Witwatersrand.

What are the three worm Nobel Prizes? ›

“For these discoveries, Brenner, Sulston and Horvitz were awarded the Nobel Prize in Physiology or Medicine in 2002. C. elegans allowed the development of a key tool in biomedical research, gene silencing by RNA interference,5 which earned Fire and Mello the Nobel Prize in Physiology or Medicine in 2006.

Who discovered the genetic code? ›

Marshall Nirenberg discovered the genetic code. He won the Nobel prize in 1968 along with Robert W. Holley and Har Gobind Khorana for deciphering the genetic code. Nirenberg and Johann Matthaei conducted experiments on protein synthesis using synthetic RNA.

Who is the father of RNA? ›

He named the material 'nuclein' since it was found in the nucleus. Leslie Orgel is the father of the RNA. He was a chemist and established a world theory of the origin of life. RNA is present in all biological cells.

Who discovered RNA and DNA? ›

Detection of significant levels of uracil by LC-UV-MS demonstrates that Miescher isolated both forms of nucleic acid-DNA and RNA-and underlines the fundamental nature of his discovery for the field of molecular genetics.

Why did Brenner start the program? ›

Brenner learns about the existence of Dimension X through his father when he tells him what he had seen during Philadelphia Experiment before dying. After that, tapping into Dimension X became Martin's life work, which led him to begin the Nevada Experiment.

Who discovered C. elegans? ›

A key figure of this phase is Emile Maupas, a professional archivist and librarian living in Algiers and working on biology as a personal interest (see Appendix 3, Section 18.1). He was the first to isolate and name Rhabditis elegans (now Caenorhabditis elegans) (Maupas, 1900).

What major discoveries were made in C. elegans? ›

TABLE 2 Selected discoveries in C. elegans research
YearDiscovery
1983First complete metazoan cell lineage
1983Discovery of apoptosis (cell death) genes
1984Identification of heterochronic genes
1986First complete wiring diagram of a nervous system
27 more rows

What happened in the Crick and Brenner experiment when two nucleotides were added to the gene of a virus? ›

This was later confirmed experimentally; Francis Crick and Sydney Brenner used the chemical mutagen proflavin to insert one, two, or three nucleotides into the gene of a virus. When one or two nucleotides were inserted, protein synthesis was completely abolished.

What was the Crick codon experiment? ›

The experiment

When nucleotides were inserted or deleted, the gene would often be nonfunctional. However, if three base pairs were added or deleted, the gene would remain functional. This proved that the genetic code uses a codon of three nucleotide bases that corresponds to an amino acid.

What discoveries by Brenner Sulston and Horvitz led to the Nobel Prize? ›

Sulston and H. Robert Horvitz, won the Nobel Prize for Physiology or Medicine in 2002 for their discoveries about how genes regulate tissue and organ development via a key mechanism called programmed cell death, or apoptosis. After receiving a Ph. D.

References

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