Abstract

The nematode Caenorhabditis elegans has become one of the most widely used model systems for the study of aging, yet very little is known about how C. elegans age. The development of the worm, from egg to young adult has been completely mapped at the cellular level, but such detailed studies have not been extended throughout the adult lifespan. Numerous single gene mutations, drug treatments and environmental manipulations have been found to extend worm lifespan. To interpret the mechanism of action of such aging interventions, studies to characterize normal worm aging, similar to those used to study worm development are necessary. We have used 4′,6′-diamidino-2-phenylindole hydrochloride staining and quantitative polymerase chain reaction to investigate the integrity of nuclei and quantify the nuclear genome copy number of C. elegans with age. We report both systematic loss of nuclei or nuclear DNA, as well as dramatic age-related changes in nuclear genome copy number. These changes are delayed or attenuated in long-lived daf-2 mutants. We propose that these changes are important pathobiological characteristics of aging nematodes.

Highlights

  • Aging is generally defined and studied as a population phenomenon

  • We identified a striking heterogeneity among middle-aged nematodes with respect to nuclear genome copy number, as well as a systematic loss of nuclear genome copy number with age in both wild-type and long-lived nematodes

  • Nuclei are systematically lost with age in wild-type and long-lived Caenorhabditis elegans

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Summary

Introduction

Aging is generally defined and studied as a population phenomenon. Yet some aspects of aging, such as differences in individual lifespans, can only be understood through the study of individuals. An enigmatic aspect of aging is the heterogeneity in lifespan experienced by individuals of a synchronized population (Finch, 1990; Finch & Kirkwood, 2000). In addition to being genetically identical, young adult worms are essentially physically identical; studies of nematode development have mapped the cellular divisions and migrations leading to the final location of each of the 959 somatic nuclei in the young adult worm. Such studies of worm morphology have not been applied to the remainder of the nematode lifespan

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