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History of the science of mutagenesis from a personal perspective
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AbstractA career in the study of mutagenesis spanning 50 years is a gift few scientists have been bestowed. My tenure in the field started in 1953, the year the structure of DNA became known (Watson and Crick [1953]: Nature 171:737). Before that time, it was suspected that DNA was the genetic material based on the research of Oswald T. Avery (Avery et al. [1944]: J Exp Med 79:137), but many scientists still believed that proteins or polysaccharides could be the genetic material. The present article describes a lifetime of personal experience in the field of chemical mutagenesis. The methods used to treat viruses with chemical mutagens were well developed in the 1950s. Here I review the early use of nitrous acid and hydroxylamine as mutagens in eukaryotes, the development of methods for the metabolic activation of mutagens by microsomal preparations, and the selection of a mutant tester set for the qualitative characterization of the mutagenic activity of chemicals. These studies provided critical background information that was used by Bruce Ames in the development of his Salmonella/microsome assay, widely known as the Ames test (Ames et al. [1973]: Proc Nat Acad Sci USA 70:2281–2285). This article also describes how a set of diagnostic chemical mutagens was selected and used to identify the molecular nature of gene mutations. Today, DNA sequencing has replaced the use of diagnostic mutagens, but studies of this kind formed the foundation of modern mutation research. They also helped set the stage for the organization of the Environmental Mutagen Society and the Environmental Mutagen Information Center, which are described. The article ends with the development of mammalian single‐cell mutation assays, the first system for studying in vivo mutagenesis using recoverable vectors in transgenic animals, other mutation assays in intact mammals, and my thoughts on the critically important area of germ cell mutagenesis. This narrative is not a complete autobiographical account, in that I have selected only those experiences that I feel are important for the history of the field and the edification of today's students. I hope I have shown that science not only is a valuable pursuit but can also be fun, stimulating, and satisfying. A good sense of humor and the knowledge that many discoveries come by serendipity are essential. Environ. Mol. Mutagen., 2004. Published 2004 Wiley‐Liss, Inc.
Title: History of the science of mutagenesis from a personal perspective
Description:
AbstractA career in the study of mutagenesis spanning 50 years is a gift few scientists have been bestowed.
My tenure in the field started in 1953, the year the structure of DNA became known (Watson and Crick [1953]: Nature 171:737).
Before that time, it was suspected that DNA was the genetic material based on the research of Oswald T.
Avery (Avery et al.
[1944]: J Exp Med 79:137), but many scientists still believed that proteins or polysaccharides could be the genetic material.
The present article describes a lifetime of personal experience in the field of chemical mutagenesis.
The methods used to treat viruses with chemical mutagens were well developed in the 1950s.
Here I review the early use of nitrous acid and hydroxylamine as mutagens in eukaryotes, the development of methods for the metabolic activation of mutagens by microsomal preparations, and the selection of a mutant tester set for the qualitative characterization of the mutagenic activity of chemicals.
These studies provided critical background information that was used by Bruce Ames in the development of his Salmonella/microsome assay, widely known as the Ames test (Ames et al.
[1973]: Proc Nat Acad Sci USA 70:2281–2285).
This article also describes how a set of diagnostic chemical mutagens was selected and used to identify the molecular nature of gene mutations.
Today, DNA sequencing has replaced the use of diagnostic mutagens, but studies of this kind formed the foundation of modern mutation research.
They also helped set the stage for the organization of the Environmental Mutagen Society and the Environmental Mutagen Information Center, which are described.
The article ends with the development of mammalian single‐cell mutation assays, the first system for studying in vivo mutagenesis using recoverable vectors in transgenic animals, other mutation assays in intact mammals, and my thoughts on the critically important area of germ cell mutagenesis.
This narrative is not a complete autobiographical account, in that I have selected only those experiences that I feel are important for the history of the field and the edification of today's students.
I hope I have shown that science not only is a valuable pursuit but can also be fun, stimulating, and satisfying.
A good sense of humor and the knowledge that many discoveries come by serendipity are essential.
Environ.
Mol.
Mutagen.
, 2004.
Published 2004 Wiley‐Liss, Inc.
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