Journal Article DZNE-2022-00524

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CEST‐2.2 overexpression alters lipid metabolism and extends longevity of mitochondrial mutants

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2022
Wiley Hoboken, NJ [u.a.]

EMBO reports 23(5), e52606 () [10.15252/embr.202152606]

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Abstract: Mitochondrial dysfunction can either extend or decrease Caenorhabditis elegans lifespan, depending on whether transcriptionally regulated responses can elicit durable stress adaptation to otherwise detrimental lesions. Here, we test the hypothesis that enhanced metabolic flexibility is sufficient to circumvent bioenergetic abnormalities associated with the phenotypic threshold effect, thereby transforming short-lived mitochondrial mutants into long-lived ones. We find that CEST-2.2, a carboxylesterase mainly localizes in the intestine, may stimulate the survival of mitochondrial deficient animals. We report that genetic manipulation of cest-2.2 expression has a minor lifespan impact on wild-type nematodes, whereas its overexpression markedly extends the lifespan of complex I-deficient gas-1(fc21) mutants. We profile the transcriptome and lipidome of cest-2.2 overexpressing animals and show that CEST-2.2 stimulates lipid metabolism and fatty acid beta-oxidation, thereby enhancing mitochondrial respiratory capacity through complex II and LET-721/ETFDH, despite the inherited genetic lesion of complex I. Together, our findings unveil a metabolic pathway that, through the tissue-specific mobilization of lipid deposits, may influence the longevity of mitochondrial mutant C. elegans.

Keyword(s): Animals (MeSH) ; Caenorhabditis elegans: metabolism (MeSH) ; Caenorhabditis elegans Proteins: genetics (MeSH) ; Caenorhabditis elegans Proteins: metabolism (MeSH) ; Lipid Metabolism: genetics (MeSH) ; Longevity: genetics (MeSH) ; Mitochondria: metabolism (MeSH)

Classification:

Contributing Institute(s):
  1. Aging and neurodegeneration (AG Bano)
  2. Translational Biogerontology (AG Ehninger)
  3. United epigenomic platform (AG Schultze)
  4. Platform for Single Cell Genomics and Epigenomics at DZNE & University of Bonn (R&D PRECISE)
  5. Scientific board (Scientific board)
Research Program(s):
  1. 351 - Brain Function (POF4-351) (POF4-351)
  2. 352 - Disease Mechanisms (POF4-352) (POF4-352)
  3. 354 - Disease Prevention and Healthy Aging (POF4-354) (POF4-354)

Appears in the scientific report 2022
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Medline ; Creative Commons Attribution-NonCommercial-NoDerivs CC BY-NC-ND 4.0 ; OpenAccess ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Wiley ; Essential Science Indicators ; IF >= 5 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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Institute Collections > BN DZNE > BN DZNE-Scientific board
Institute Collections > BN DZNE > BN DZNE-R&D PRECISE
Document types > Articles > Journal Article
Institute Collections > BN DZNE > BN DZNE-AG Ehninger
Institute Collections > BN DZNE > BN DZNE-PRECISE
Institute Collections > BN DZNE > BN DZNE-AG Bano
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Linked articles:

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Dataset  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;
Dataset: CEST-2.2 stimulates lipid metabolism and promotes longevity in mitochondrial mutant animals (RNA-Seq)
Gene Expression Omnibus ()   Download fulltextFulltext BibTeX | EndNote: XML, Text | RIS

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Dataset
Dataset: CEST-2.2 stimulates lipid metabolism and promotes longevity in mitochondrial mutant animals (SuperSeries)
Gene Expression Omnibus ()   Download fulltextFulltext BibTeX | EndNote: XML, Text | RIS

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Dataset  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;
Dataset: CEST-2.2 stimulates lipid metabolism and promotes longevity in mitochondrial mutant animals (ChIP-Seq)
Gene Expression Omnibus ()   Download fulltextFulltext BibTeX | EndNote: XML, Text | RIS


 Record created 2022-04-25, last modified 2024-03-20


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