Don Brown’s experiments revolutionized our understanding of how a fertilized egg develops into the grownup organism. His analysis on the interface of molecular biology, embryology and biochemistry was seminal in shifting the main focus of developmental biology from anatomical observations by microscopes to mechanistic research of genes and their regulation. Brown’s early work on remoted genes led to the introduction of recombinant DNA — when it turned attainable to instantly modify the genes of organisms. It additionally supplied the inspiration for focused genetic engineering.

Born in Cincinnati, Ohio, Brown did an undergraduate diploma at Dartmouth School in Hanover, New Hampshire, and medical and grasp’s levels on the College of Chicago Medical Faculty in Illinois. He selected a profession in analysis after a journal-club dialogue of James Watson and Francis Crick’s basic 1953 Nature paper on the construction of DNA. Fascinated by how embryos develop, Brown determined to give attention to the position of DNA in growth.

After a 12 months as an intern at Charity Hospital in New Orleans, Louisiana, and two years on the Nationwide Institutes of Well being in Bethesda, Maryland, Brown spent a formative 12 months on the Pasteur Institute in Paris finding out gene regulation in micro organism. This was the place the sector of molecular biology was being born; and he was stimulated by lunchtime discussions led by future Nobel laureates Jacques Monod, François Jacob and André Lwoff.

EU proposal on CRISPR-edited crops is welcome — however not sufficient

In 1961, Brown returned to the US and joined the Carnegie Establishment’s Division of Embryology in Baltimore, Maryland, as its first biochemist. He stayed there till he retired in 2005, appearing as its director from 1976 to 1994, throughout which period the division turned world-renowned.

At Carnegie, he determined to discover the molecular foundation of embryo growth, utilizing the African clawed frog (Xenopus laevis). In step one of gene expression, segments of DNA are copied by transcription to supply RNA. Within the subsequent step, ribosomes (containing ribosomal RNA, rRNA) function the mobile factories for synthesizing proteins. Along with British developmental biologist John Gurdon, Brown discovered {that a} Xenopus mutant missing nucleoli (spherical buildings contained in the cell’s nucleus) neither made rRNA nor had rRNA genes — and due to this fact that the nucleolus makes the rRNA part of ribosomes.

He additionally deduced that wholesome Xenopus eggs (oocytes) within the ovary which have hundreds of nucleoli have further copies of rRNA genes. This discovery of ‘gene amplification’ was revealed in a seminal paper in 1968 (D. D. Brown and I. B. Dawid Science 160, 272–280; 1968); US cell biologist Joseph Gall reported the same end result independently the identical 12 months. The discovering challenged the concept that all of the cells of an organism have a relentless quantity of DNA. It’s now additionally appreciated that gene amplification generally is a hallmark of most cancers. Brown’s 1968 work concerned gene isolation earlier than the times of DNA cloning, and the large quantity of amplified rRNA genes from Xenopus oocytes was purified by centrifugation. This was the primary time a gene had been purified, and others used this materials to clone the primary eukaryotic gene, thus launching the recombinant-DNA period.

Paul Berg (1926–2023)

Subsequent, Brown explored the regulation of gene exercise for an additional part of the ribosome: 5S RNA. In 1979, he attended the Gordon convention on Developmental Biology in Andover, New Hampshire to current his findings. On the opening social occasion, phrase about Brown’s outcomes unfold like wildfire. By the point he gave his discuss a number of days later, everybody within the viewers already knew the punchline — gene exercise was managed by an ‘inside management area’ that lay in the course of the 5S RNA gene, not earlier than the gene as had been anticipated.

Quickly afterwards, a protein was discovered that sure to the interior management area of the 5S RNA gene. This was the inaugural instance of a ‘gene-specific transcription issue’. Robert Roeder, who had beforehand executed a postdoc with Brown, purified, cloned and sequenced it. In subsequent research by British biophysicist Aaron Klug, the issue additionally turned the primary instance of a ‘zinc finger protein’ — by which zinc is sure to a stretch of amino acids.

The power to engineer zinc finger proteins so that they bind to particular genes ushered within the first wave of the genome-editing revolution twenty years in the past. Focused genetic engineering, now broadly practised utilizing CRISPR–Cas nucleases, owes a formidable debt to Brown’s work.

Don’s closing research had been on amphibian metamorphosis. His identification of genes managed by thyroid hormone supplied perception into the hormonal management of organ growth, cell progress and programmed cell demise.

Don was a scientific chief. He obtained the 2012 Lasker–Koshland Particular Achievement Award, organized the primary Developmental Biology Gordon Convention in 1970 and was president of the US Society for Developmental Biology and the American Society for Cell Biology (ASCB). He was dedicated to younger scientists and based and led the Life Sciences Analysis Basis, which awards postdoctoral fellowships in the US.

Don had a bottom-up and democratic view of management. He revealed profiles of researchers within the ASCB publication to make everybody really feel a part of the society ‘household’. He was an incredible administrator, being easy, sincere and approachable. He was a humble man with an incredible sense of humour. Don was a beautiful one that impressed the scientific group by his analysis, his management and his mentorship of the rising technology. He will likely be missed.

Competing Pursuits

The creator declares no competing pursuits.