| 1984:    Recombination at the DNA Level, Vol. XLIXOrganizer: Amar J. S. Klar and Jeffrey N. Strathern  The previous Symposium with “recombination” in the 
                title had been held only six years before, and then recombination 
                had formed the smaller part of the meeting that included also 
                replication. Recombination had also been part of the Symposium 
                on Movable Genetic Elements. Why was it felt that a third meeting 
                was needed, three in the space of six years? The main reason was that Frank Stahl’s prediction in his 
                summary of the 1978 meeting had come true–the torch had 
                passed from the geneticists to the biochemists. Moreover, recombinant 
                DNA tools and techniques were now part and parcel of research 
                and no longer restricted to a small coterie of laboratories. This 
                meant that great science was being done by many more and this 
                was reflected in the great diversity of the studies reported in 
                this Symposium. Indeed, Alan Campbell in his summary commented 
                on this diversity and would not predict whether common principles 
                would ever emerge to unify recombination in all these systems. A large number of studies used movable genetic elements as tools 
                to analyze the integration of these DNA molecules as models for 
                recombination at the chromosome scale. The bacterial transposons 
                Tn5  | 
and Tn10 were in evidence, as well as a set of papers reporting 
                studies using the bacteriophage Mu. Research on Mu had been promoted 
                by Ahmed Bukhari at Cold Spring Harbor Laboratory. Just a few 
                months after the Symposium, and at the tragically young aged of 
                40, Bukhari died of a heart attack. The volume was dedicated to 
                him. A very interesting set of papers dealt with recombination in 
                mammalian cells, between plasmids introduced into the cells, between 
                two introduced plasmids, and a plasmid and sequences integrated 
                into the chromosome. These studies led a few years later to practicable 
                methods for manipulating genes in mammalian cells and, when applied 
                to mouse embryonic stem cells, to the ability to change very precisely 
                DNA sequences in a mouse.
 — Jan A. Witkowski |