"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.

Radiation Research
|June 25, 2024
PubMed

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 Alleles02:41

Lethal Alleles

Agouti: A Lethal Allele
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...
15.4K
Mutations01:39

Mutations

Overview
81.8K
Mismatch Repair01:20

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
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...
4.8K
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
13.9K
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
10.6K
Genome Copying Errors02:46

Genome Copying Errors

DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
4.2K