Aging
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Research Paper|Volume 5, Issue 6|pp 394—411

Age-related micro-RNA abundance in individual C. elegans

Mark Lucanic1, Jill Graham1, Gary Scott1, Dipa Bhaumik1, Christopher C. Benz1, Alan Hubbard1,2, Gordon J. Lithgow1, Simon Melov1
  • 1Buck Institute for Research on Aging, 8001 Redwood Boulevard, Novato, CA 94945, USA
  • 2Division of Biostatistics, University of California, Berkeley, Berkeley, CA 94720, USA
Received: June 1, 2013Accepted: June 11, 2013Published: June 12, 2013

Copyright: © 2013 Lucanic et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Non-coding small RNAs of the micro-RNA class (miRNA) are conserved regulators of gene function with a broad impact on biological processes. We screened miRNA levels for age-related changes in individual worms and investigated their influence on the lifespan of the nematode C. elegans. We measured the abundance of 69 miRNAs expressed in individual animals at different ages with over thirty five thousand discrete quantitative nano-fluidic polymerase chain reactions. We found that miRNA abundance was highly variable between individual worms raised under identical conditions and that expression variability generally increased with age. To identify expression differences associated with either reproductive or somatic tissues, we analyzed wild type and mutants that lacked germlines. miRNAs from the mir-35-41 cluster increased in abundance with age in wild type animals, but were nearly absent from mutants lacking a germline, suggesting their age-related increase originates from the germline. Most miRNAs with age-dependent levels did not have a major effect on lifespan, as corresponding deletion mutants exhibited wild-type lifespans. The major exception to this was mir-71, which increased in abundance with age and was required for normal longevity. Our genetic characterization indicates that mir-71 acts at least partly in parallel to insulin/IGF like signals to influence lifespan.