Related Experiment Video
Updated: Jun 23, 2025

A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions
Published on: May 27, 2021
"Lethal Mutations" a Misnomer or the Start of a Scientific Revolution?
Carmel Mothersill1, Rhea Desai1, Colin B Seymour1
1Department of Biology, McMaster University, Hamilton, Ontario, Canada.
Abstract:
The aim of this paper is to review the history surrounding the discovery of lethal mutations, later described as delayed reproductive death. Lethal mutations were suggested very early on, to be due to a generalised instability in a cell population and are considered now to be one of the first demonstrations of "radiation-induced genomic instability" which led later to the establishment of the field of "non-targeted effects." The phenomenon was first described by Seymour et al. in 1986 and was confirmed by Trott's group in Europe and by Little and colleagues in the United States before being extended by Mendonca et al. in 1989, who showed conclusively that the distinguishing feature of lethal mutation occurrence was that it happened suddenly after about 9-10 population doublings in progeny which had survived the original dose of ionizing radiation. However, many authors then suggested that in fact, lethal mutations were implicit in the original experiments by Puck and Marcus in 1956 and were described in the extensive work by Sinclair in 1964, who followed clonal progeny for up to a year after irradiation and described "small colony formation" as a persistent consequence of ionizing radiation exposure. In this paper, we examine the history from 1956 to the present using the period from 1986-1989 as an anchor point to reach into the past and to go forward through the evolution of the field of low dose radiobiology where non-targeted effects predominate.
Insights
Lethal mutations, or delayed reproductive death, were early indicators of radiation-induced genomic instability. This review traces their discovery and connection to non-targeted effects in low dose radiobiology.
Area of Science:
- Radiobiology
- Genetics
- Genomics
Background:
- Lethal mutations, termed delayed reproductive death, were initially attributed to general cell population instability.
- They are now recognized as early evidence of radiation-induced genomic instability.
- This phenomenon laid groundwork for the field of non-targeted effects.
Purpose of the Study:
- To review the historical discovery and evolution of lethal mutations.
- To examine the link between early observations and modern understanding of non-targeted effects.
- To trace the development of low dose radiobiology.
Main Methods:
- Historical review of scientific literature from 1956 to present.
- Focus on key studies from 1986-1989 as an anchor point.
- Analysis of early descriptions of radiation effects on cell populations.
Main Results:
- Lethal mutations were first described in 1986, with confirmation and extension in subsequent years.
- Evidence suggests these effects were implicit in earlier work (Puck and Marcus, 1956; Sinclair, 1964).
- A key feature is sudden occurrence after 9-10 population doublings post-irradiation.
Conclusions:
- Lethal mutations represent a significant early finding in radiobiology.
- The study of these mutations evolved into the field of non-targeted effects.
- Understanding these effects is crucial in low dose radiobiology.
Related Concept Videos
Lethal Alleles
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Mutations
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
In-vitro Mutagenesis
Nonsense-mediated mRNA Decay
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Genome Copying Errors

