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Identification of healthspan-promoting genes in Caenorhabditis elegans based on a human GWAS study.
Saul, Nadine; Dhondt, Ineke; Kuokkanen, Mikko; Perola, Markus; Verschuuren, Clara; Wouters, Brecht; von Chrzanowski, Henrik; De Vos, Winnok H; Temmerman, Liesbet; Luyten, Walter; Zecic, Aleksandra; Loier, Tim; Schmitz-Linneweber, Christian; Braeckman, Bart P.
Affiliation
  • Saul N; Molecular Genetics Group, Institute of Biology, Humboldt University of Berlin, Berlin, Germany. nadine.saul@gmx.de.
  • Dhondt I; Laboratory of Aging Physiology and Molecular Evolution, Biology Department, Ghent University, Ghent, Belgium.
  • Kuokkanen M; Genomics and Biomarkers Unit, Department of Health, National Institute for Health and Welfare, Helsinki, Finland.
  • Perola M; Department of Human Genetics and South Texas Diabetes and Obesity Institute, School of Medicine, The University of Texas Rio Grande Valley, Brownsville, TX, USA.
  • Verschuuren C; Genomics and Biomarkers Unit, Department of Health, National Institute for Health and Welfare, Helsinki, Finland.
  • Wouters B; Laboratory of Aging Physiology and Molecular Evolution, Biology Department, Ghent University, Ghent, Belgium.
  • von Chrzanowski H; Biology Department, KU Leuven, Leuven, Belgium.
  • De Vos WH; Molecular Genetics Group, Institute of Biology, Humboldt University of Berlin, Berlin, Germany.
  • Temmerman L; The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
  • Luyten W; Laboratory of Cell Biology and Histology, Department of Veterinary Sciences, University of Antwerp, Antwerp, Belgium.
  • Zecic A; Biology Department, KU Leuven, Leuven, Belgium.
  • Loier T; Biology Department, KU Leuven, Leuven, Belgium.
  • Schmitz-Linneweber C; Laboratory of Aging Physiology and Molecular Evolution, Biology Department, Ghent University, Ghent, Belgium.
  • Braeckman BP; Laboratory of Aging Physiology and Molecular Evolution, Biology Department, Ghent University, Ghent, Belgium.
Biogerontology ; 23(4): 431-452, 2022 08.
Article in En | MEDLINE | ID: mdl-35748965
To find drivers of healthy ageing, a genome-wide association study (GWAS) was performed in healthy and unhealthy older individuals. Healthy individuals were defined as free from cardiovascular disease, stroke, heart failure, major adverse cardiovascular event, diabetes, dementia, cancer, chronic obstructive pulmonary disease (COPD), asthma, rheumatism, Crohn's disease, malabsorption or kidney disease. Six single nucleotide polymorphisms (SNPs) with unknown function associated with ten human genes were identified as candidate healthspan markers. Thirteen homologous or closely related genes were selected in the model organism C. elegans for evaluating healthspan after targeted RNAi-mediated knockdown using pathogen resistance, muscle integrity, chemotaxis index and the activity of known longevity and stress response pathways as healthspan reporters. In addition, lifespan was monitored in the RNAi-treated nematodes. RNAi knockdown of yap-1, wwp-1, paxt-1 and several acdh genes resulted in heterogeneous phenotypes regarding muscle integrity, pathogen resistance, chemotactic behaviour, and lifespan. Based on these observations, we hypothesize that their human homologues WWC2, CDKN2AIP and ACADS may play a role in health maintenance in the elderly.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / Caenorhabditis elegans Proteins Type of study: Diagnostic_studies Limits: Aged / Animals / Humans Language: En Journal: Biogerontology Journal subject: GERIATRIA Year: 2022 Type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / Caenorhabditis elegans Proteins Type of study: Diagnostic_studies Limits: Aged / Animals / Humans Language: En Journal: Biogerontology Journal subject: GERIATRIA Year: 2022 Type: Article Affiliation country: Germany