P. Starlinger – författare

The 35th N:osbach Colloquium "The Impact of Gene Transfer Techniques in Eukaryotic CeU Biology" brought together a number of speakers interested in various aspects of cellular and developmental biology and over 600 other scientists, who listened to the lectures and participated in the lively discussions. The questions and experiments described were very varied, but all of them illustrated the importance of recombinant DNA technology. The powerful techniques of identifying and isolating DNA sequences, followed by their introduction into living cells and even into the germ cells of multicellular organisms, have pervaded nearly every branch of molecular biology. The presentations and discussions that followed showed that recombinant DNA has tremendously increased our potential for fundamental research. Now, and for some time to corne, these contri­ butions and the resulting increase in our understanding of life will be the main result of gene manipulation. There will, however, also be applications that will lead to new industrial processes. One section was devoted to novel ways of vaccine production and another to herbicide resistance. These applications are a matter of intense debate in the public domain today. Although they reach beyond the scope of the research labora.tory at a university or research institution, scientists have the knowledge necessary to judge these developments and are sometimes directly involved. There­ fore the development of industrial qene technology requires the attention of the whole scientific community. We hope that this Symposium has also served this purpose.

The 35th N:osbach Colloquium "The Impact of Gene Transfer Techniques in Eukaryotic CeU Biology" brought together a number of speakers interested in various aspects of cellular and developmental biology and over 600 other scientists, who listened to the lectures and participated in the lively discussions. The questions and experiments described were very varied, but all of them illustrated the importance of recombinant DNA technology. The powerful techniques of identifying and isolating DNA sequences, followed by their introduction into living cells and even into the germ cells of multicellular organisms, have pervaded nearly every branch of molecular biology. The presentations and discussions that followed showed that recombinant DNA has tremendously increased our potential for fundamental research. Now, and for some time to corne, these contri­ butions and the resulting increase in our understanding of life will be the main result of gene manipulation. There will, however, also be applications that will lead to new industrial processes. One section was devoted to novel ways of vaccine production and another to herbicide resistance. These applications are a matter of intense debate in the public domain today. Although they reach beyond the scope of the research labora.tory at a university or research institution, scientists have the knowledge necessary to judge these developments and are sometimes directly involved. There­ fore the development of industrial qene technology requires the attention of the whole scientific community. We hope that this Symposium has also served this purpose.

The topic of this years'' ~osbach Colloquium was DNA integration. We have tried to bring together experts from different fields of research who are studying natural processes by which DNA molecules from differ­ ent sources are linked. It has been known for a long time that such linkage occurs between the chromosomes of bacteriophages and plasmids on the one hand and the chromosome of the bacterial host on the other. This process has been especially well studied in bacteriophage A. Since it is controlled in a complicated way, we began with a lecture by M. ptashne on these regulatory processes. H. Nash described the inte­ gration of bacteriophage A into the bacterial chromosome. To put this site-specific process into perspective, G. Mosig lectured on genetic recombination in prokaryotes in general and K. Murray described the use of bacteriophage A as an artificial vector for genetic engineering. A different kind of bacteriophage integration is shown by bacteriophage Mu, which is much less specific in its choice of an integration site than A. The properties of this phage were described by P. van de Putte.