Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Heredity
  • View all journals
  • Search
  • Log in
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. heredity
  3. original article
  4. article
The effects of gene-environment interaction on the expression of longevity
Download PDF
Download PDF
  • Original Article
  • Published: 01 August 1985

The effects of gene-environment interaction on the expression of longevity

  • Michael J Clare1 &
  • Leo S Luckinbill1 

Heredity volume 55, pages 19–26 (1985)Cite this article

  • 1360 Accesses

  • 119 Citations

  • 3 Altmetric

  • Metrics details

Abstract

Several previous attempts at selecting for increased life span with Drosophila have failed to obtain a response to selection, and postulate that life span is controlled by non-genetic maternal effects instead of genes. In other experiments, however, populations have responded. This study uses a set of true-breeding long- and short-lived stocks developed by in vitro selection to examine the effect on life span of developmental environment and outcrossing.

The expression of genes for life span is shown here to vary as a result of a gene-environment interaction and is strongly affected by the environment during development. The longevity of F1 crosses between long- and short-lived parental lines is additive when the density of larvae is high and unfixed, showing that life span is controlled by genes and not nongenetic maternal effects. But, when numbers of larvae are held low and constant, as in studies where selection fails, life span of crosses and parental lines is greatly restricted. The failure of some previous attempts at selection, therefore, appears to have resulted from the introduction, through experimental design, of strong artifactual environmental effects that limit the phenotypic expression of genes for life span and the effectiveness of selection.

Comparison of fecundity in parental and F1 lines shows that selection for increased life span antagonistically reduces early-life fecundity. Short-lived, parental lines, reproduced at an early age in life, lay 22–24 per cent more eggs in the same period than do long-lived lines selected for reproduction at a late age.

Similar content being viewed by others

A life-history allele of large effect shortens developmental time in a wild insect population

Article 13 November 2023

Dietary stress remodels the genetic architecture of lifespan variation in outbred Drosophila

Article 22 December 2022

Reproductive individuality of clonal fish raised in near-identical environments and its link to early-life behavioral individuality

Article Open access 24 November 2023

Article PDF

References

  • Charlesworth, B. 1980. Evolution in Age-structured Populations. Cambridge University Press, Cambridge.

    Google Scholar 

  • Derr, J A. 1980. The nature of variation in life history characters of Dysdercus bimaculatus (Heteroptera: Pyrrhocoridae), a colonizing species. Evolution, 34, 548–557.

    Article  PubMed  Google Scholar 

  • Flanagan, J R. 1980. Detecting early-life components in the determination of the age of death. Mech Aging Dev, 13, 41–62.

    Article  CAS  PubMed  Google Scholar 

  • Lansing, A I. 1947. A transmissible, cumulative and reversible factor in aging. J Gerontol, 2, 228–239.

    Article  CAS  PubMed  Google Scholar 

  • Lansing, A I. 1954. A nongenetic factor in the longevity of rotifers. Ann N Y Acad Sci, 57, 455–464.

    Article  CAS  PubMed  Google Scholar 

  • Lerner, I M. 1954. Genetic Homeostasis. Wiley, New York.

    Google Scholar 

  • Lints, F A, and Gruwez, G. 1972. What determines the duration of development in Drosophila melanogaster. Mech Aging Dev, 1, 285–297.

    Google Scholar 

  • Lints, F A, and Hoste, C. 1974. The Lansing Effect revisited. I. Life span. Exper Gerontol, 9, 51–69.

    Article  CAS  Google Scholar 

  • Lints, F A, and Hoste, C. 1977. The Lansing Effect revisited. II. Cumulative and spontaneously reversible effects on fecundity in Drosophila melanogaster. Evolution, 38(6), 996–1003.

    Google Scholar 

  • Lints, F A, Stoll, J A, Gruwez, G, and Lints, C V. 1979. An attempt to select for increased longevity in Drosophila melanogaster. Gerontol, 5, 192–204.

    Article  Google Scholar 

  • Luckinbill, L S, Arking, R, Clare, M J, Cirocco, W, and Buck, S A. 1984. Selection for delayed senescence in Drosophila melanogaster. Evolution, 3(5), 996–1003.

    Article  Google Scholar 

  • Luckinbill, L S, Clare, M J. Selection for life span in Drosophila melanogaster. 1985. Heredity, 55, 9–18.

    Article  PubMed  Google Scholar 

  • Medawar, P B. 1952. An Unsolved Problem in Biology. Lewis, London.

  • Murphy, P A, Giesel, J T, and Manlove, M N. 1983. Temperature effects on life history variation in Drosophila simulans. Evolution, 37, 1181–1191.

    Article  CAS  PubMed  Google Scholar 

  • Parsons, P A. 1978. The genetics of aging in optimal and stressful environments. Exp Gerontol, 13, 357–363.

    Article  CAS  PubMed  Google Scholar 

  • Parsons, P A. 1977. Genotype-temperature interactions for longevity in Drosophila simulans. Exp Gerontol, 12, 241–244.

    Article  CAS  PubMed  Google Scholar 

  • Rose, M R. 1984. Laboratory evolution of postponed senescence in Drosophila melanogaster. Evolution, 38(5), 1004–1009.

    Article  PubMed  Google Scholar 

  • Rose, M R, and Charlesworth, B. 1980. A test of evolutionary theories of senescence. Nature, 287, 141–142.

    Article  CAS  PubMed  Google Scholar 

  • Rose, M R, and Charlesworth, B. 1981. Genetics of life history in Drosophila melanogaster. II. Exploratory selection experiments. Genetics, 97, 187–196.

    CAS  PubMed  PubMed Central  Google Scholar 

  • Waddington, C H. 1957. The strategy of the Genes. Allen and Unwin, London.

  • Waddington, C H. 1961. Genetic Assimilation. Adv Gen, 10, 257–293.

    Article  CAS  Google Scholar 

  • Williams, G C. 1957. Pleiotropy, natural selection and the evolution of senescence. Evolution, 11, 398–411.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Department of Biological Sciences, Wayne State University, Detroit, 48202, Michigan

    Michael J Clare & Leo S Luckinbill

Authors
  1. Michael J Clare
    View author publications

    Search author on:PubMed Google Scholar

  2. Leo S Luckinbill
    View author publications

    Search author on:PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Clare, M., Luckinbill, L. The effects of gene-environment interaction on the expression of longevity. Heredity 55, 19–26 (1985). https://doi.org/10.1038/hdy.1985.67

Download citation

  • Received: 05 November 1984

  • Issue date: 01 August 1985

  • DOI: https://doi.org/10.1038/hdy.1985.67

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

This article is cited by

  • Effects of telomere length in Drosophila melanogaster on life span, fecundity, and fertility

    • Marika F. Walter
    • Max R. Biessmann
    • Harald Biessmann

    Chromosoma (2007)

  • Genetic approaches to study aging in Drosophila melanogaster

    • Luc Poirier
    • Laurent Seroude

    AGE (2005)

  • Genetic analysis of ageing: role of oxidative damage and environmental stresses

    • George M. Martin
    • Steven N. Austad
    • Thomas E. Johnson

    Nature Genetics (1996)

  • Inherited stress resistance and longevity: a stress theory of ageing

    • Peter A Parsons

    Heredity (1995)

  • Chromosomal localization and regulation of the longevity determinant genes in a selected strain of Drosophila melanogaster

    • Steven Buck
    • Robert A Wells
    • Robert Arking

    Heredity (1993)

Download PDF

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Podcasts
  • Current issue
  • Collections
  • Follow us on Twitter
  • Sign up for alerts
  • RSS feed

About the journal

  • Journal Information
  • Open access publishing
  • About the Editors
  • Contact
  • About the Partner
  • For Advertisers
  • Subscribe

Publish with us

  • For Authors & Referees
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Heredity (Heredity)

ISSN 1365-2540 (online)

ISSN 0018-067X (print)

nature.com sitemap

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2025 Springer Nature Limited