Genetic diversity estimates for the Caenorhabditis Intervention Testing Program screening panel

Anastasia A Teterina1,2, Anna L Coleman-Hulbert1, Stephen A Banse1

  • 1Institute of Ecology and Evolution, University of Oregon, Eugene, OR, 97403, USA.

Micropublication Biology
|January 31, 2022
PubMed

Insights

The Caenorhabditis Intervention Testing Program (CITP) uses a genetically diverse panel of nematode strains to identify compounds that extend lifespan. This panel shows significant genetic diversity, suggesting findings may translate to conserved biological pathways.

Area of Science:

  • Genomics
  • Comparative Biology
  • Aging Research

Background:

  • The Caenorhabditis Intervention Testing Program (CITP) utilizes a genetically diverse panel of nematode strains to identify compounds with conserved biochemical pathway effects and mammalian translational potential.
  • The panel consists of 22 strains from three species (C. elegans, C. briggsae, C. tropicalis), collected globally to maximize inter-population genetic diversity.
  • These species are sequential hermaphrodites, simplifying experiments while maintaining intra-population homogeneity.

Purpose of the Study:

  • To estimate the genetic diversity within the CITP screening panel using publicly available and newly generated whole-genome sequences.
  • To validate the assumption that the panel encompasses broad genetic diversity for identifying broadly efficacious interventions.

Main Methods:

  • Analysis of whole-genome sequences from 22 Caenorhabditis strains across three species.
  • Calculation of average genome-wide nucleotide diversity (π) for C. elegans, C. briggsae, and C. tropicalis strains.
  • Comparison of observed genetic diversity with estimates from human and mouse populations.

Main Results:

  • Genome-wide nucleotide diversity (π) within the panel strains (C. elegans: 1.2e-3, C. briggsae: 7.5e-3, C. tropicalis: 2.6e-3) exceeds that of human populations.
  • The genetic diversity within the panel is comparable to that found in mouse populations.
  • The analysis supports the CITP's assumption of broad genetic diversity within its screening panel.

Conclusions:

  • The CITP screening panel possesses substantial genetic diversity, supporting its use for identifying lifespan-extending compounds with conserved mechanisms.
  • Compounds showing efficacy across this diverse panel are likely to act on conserved biological processes.
  • The panel's broad genetic diversity makes it a valuable resource for researchers seeking broadly efficacious interventions for various phenotypes.

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