Literature DB >> 21893079

FUdR causes a twofold increase in the lifespan of the mitochondrial mutant gas-1.

Jeremy Michael Van Raamsdonk1, Siegfried Hekimi.   

Abstract

The nematode worm Caenorhabditis elegans has been used to identify hundreds of genes that influence longevity and thereby demonstrate the strong influence of genetics on lifespan determination. In order to simplify lifespan studies in worms, many researchers have employed 5-fluoro-2'-deoxyuridine (FUdR) to inhibit the development of progeny. While FUdR has little impact on the lifespan of wild-type worms, we demonstrate that FUdR causes a dramatic, dose-dependent, twofold increase in the lifespan of the mitochondrial mutant gas-1. Thus, the concentration of FUdR employed in a lifespan study can determine whether a particular strain is long-lived or short-lived compared to wild-type.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21893079      PMCID: PMC4074524          DOI: 10.1016/j.mad.2011.08.006

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN: 0047-6374            Impact factor:   5.432


  17 in total

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Authors:  D H Mitchell; J W Stiles; J Santelli; D R Sanadi
Journal:  J Gerontol       Date:  1979-01

8.  A simple method for maintaining large, aging populations of Caenorhabditis elegans.

Authors:  S Gandhi; J Santelli; D H Mitchell; J W Stiles; D R Sanadi
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  61 in total

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Authors:  Jason F Cooper; Katie K Spielbauer; Megan M Senchuk; Saravanapriah Nadarajan; Monica P Colaiácovo; Jeremy M Van Raamsdonk
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3.  Counterbalance between BAG and URX neurons via guanylate cyclases controls lifespan homeostasis in C. elegans.

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4.  High-Content Microfluidic Screening Platform Used To Identify σ2R/Tmem97 Binding Ligands that Reduce Age-Dependent Neurodegeneration in C. elegans SC_APP Model.

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7.  C. elegans lifespan extension by osmotic stress requires FUdR, base excision repair, FOXO, and sirtuins.

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Review 10.  The paradox of mitochondrial dysfunction and extended longevity.

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