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  • 1
    Publication Date: 2002-01-19
    Description: The germ line of the nematode Caenorhabditis elegans influences life-span; when the germ-line precursor cells are removed, life-span is increased dramatically. We find that neither sperm, nor oocytes, nor meiotic precursor cells are responsible for this effect. Rather life-span is influenced by the proliferating germ-line stem cells. These cells, as well as a downstream transcriptional regulator, act in the adult to influence aging, indicating that the aging process remains plastic during adulthood. We propose that the germ-line stem cells affect life-span by influencing the production of, or the response to, a steroid hormone that promotes longevity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Arantes-Oliveira, Nuno -- Apfeld, Javier -- Dillin, Andrew -- Kenyon, Cynthia -- New York, N.Y. -- Science. 2002 Jan 18;295(5554):502-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA 94143-0448, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11799246" target="_blank"〉PubMed〈/a〉
    Keywords: *Aging ; Animals ; Caenorhabditis elegans/*cytology/genetics/growth & development/*physiology ; Caenorhabditis elegans Proteins/genetics/physiology ; Cell Differentiation ; Cell Division ; Female ; Forkhead Transcription Factors ; Genes, Helminth ; Germ Cells/*cytology/physiology ; *Longevity ; Male ; Meiosis ; Mitosis ; Mutation ; Oxidative Stress ; Stem Cells/*physiology ; Temperature ; Transcription Factors/genetics/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2012-08-28
    Description: Organisms that protect their germ-cell lineages from damage often do so at considerable cost: limited metabolic resources become partitioned away from maintenance of the soma, leaving the ageing somatic tissues to navigate survival amid an environment containing damaged and poorly functioning proteins. Historically, experimental paradigms that limit reproductive investment result in lifespan extension. We proposed that germline-deficient animals might exhibit heightened protection from proteotoxic stressors in somatic tissues. We find that the forced re-investment of resources from the germ line to the soma in Caenorhabditis elegans results in elevated somatic proteasome activity, clearance of damaged proteins and increased longevity. This activity is associated with increased expression of rpn-6, a subunit of the 19S proteasome, by the FOXO transcription factor DAF-16. Ectopic expression of rpn-6 is sufficient to confer proteotoxic stress resistance and extend lifespan, indicating that rpn-6 is a candidate to correct deficiencies in age-related protein homeostasis disorders.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vilchez, David -- Morantte, Ianessa -- Liu, Zheng -- Douglas, Peter M -- Merkwirth, Carsten -- Rodrigues, Ana P C -- Manning, Gerard -- Dillin, Andrew -- R01 AG042679/AG/NIA NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Sep 13;489(7415):263-8. doi: 10.1038/nature11315.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Glenn Center for Aging Research, Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22922647" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Caenorhabditis elegans/cytology/genetics/*metabolism/physiology ; Caenorhabditis elegans Proteins/genetics/*metabolism ; Cell Separation ; Female ; Forkhead Transcription Factors ; Gene Expression Regulation ; Germ Cells/cytology/metabolism ; Heat-Shock Response/genetics ; Homeostasis/radiation effects ; Longevity/genetics/*physiology/radiation effects ; Male ; Mutation/genetics ; Oxidative Stress/physiology ; Peptides/metabolism ; Proteasome Endopeptidase Complex/chemistry/genetics/*metabolism ; Stress, Physiological/*physiology/radiation effects ; Transcription Factors/metabolism ; Ultraviolet Rays
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
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    Nature Publishing Group (NPG)
    Publication Date: 2013-05-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wolff, Suzanne -- Dillin, Andrew -- R01 ES021667/ES/NIEHS NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2013 May 23;497(7450):442-3. doi: 10.1038/497442a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California 94720-3370, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23698438" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caenorhabditis elegans/*physiology ; Female ; Longevity/*physiology ; Male ; Mitochondria/*metabolism ; Mitochondrial Proteins/*metabolism ; Ribosomal Proteins/*metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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