Literature DB >> 23499532

Fertility and germline stem cell maintenance under different diets requires nhr-114/HNF4 in C. elegans.

Xicotencatl Gracida1, Christian R Eckmann.   

Abstract

Animals can thrive on variable food resources as a result of autonomous processes and beneficial relationships with their gut microbes [1]. Food intake elicits major physiological changes, which are counteracted by transient systemic responses that maintain homeostasis in the organism. This integration of external information occurs through cellular sensory elements, such as nuclear receptors, which modulate gene expression in response to specific cues [2]. Given the importance of germline stem cells (GSCs) for the development of the germline and the continuity of species, it is reasonable to assume that GSCs might be shielded from the negative influence of environmental perturbations. To our knowledge, however, there are no mechanisms reported that protect GSCs from harmful dietary metabolites. Using Caenorhabditis elegans as a model, we report that the somatic activity of the conserved nuclear receptor nhr-114/HNF4 protects GSC integrity from dietary metabolites. In the absence of nhr-114 and on certain bacterial diets, otherwise somatically normal animals accumulate germ cell division defects during development and become sterile. We found that, in nhr-114(-) animals, the induction of germline defects and sterility depend on bacterial metabolic status, with respect to the essential amino acid tryptophan. This illustrates an animal-microbe interaction in which somatic nuclear receptor activity preserves the germline by buffering against dietary metabolites, most likely through a somatic detoxifying response. Overall, our findings uncover an unprecedented, and presumably evolutionarily conserved, soma-to-germline axis of communication that maintains reproductive robustness on variable food resources.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23499532     DOI: 10.1016/j.cub.2013.02.034

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  39 in total

Review 1.  A Comprehensive Understanding of Dietary Effects on C. elegans Physiology.

Authors:  Jie-Jun Zhou; Lei Chun; Jian-Feng Liu
Journal:  Curr Med Sci       Date:  2019-10-14

2.  Bacterial Folates Provide an Exogenous Signal for C. elegans Germline Stem Cell Proliferation.

Authors:  Snehal N Chaudhari; Madhumati Mukherjee; Alexandra S Vagasi; Gaofeng Bi; Mohammad M Rahman; Christine Q Nguyen; Ligi Paul; Jacob Selhub; Edward T Kipreos
Journal:  Dev Cell       Date:  2016-07-11       Impact factor: 12.270

3.  Gene-diet interactions and aging in C. elegans.

Authors:  Chia An Yen; Sean P Curran
Journal:  Exp Gerontol       Date:  2016-02-26       Impact factor: 4.032

4.  Genetic adaptation to diet preserves longevity.

Authors:  Albertha J M Walhout
Journal:  Cell Metab       Date:  2014-02-04       Impact factor: 27.287

5.  Adaptive capacity to bacterial diet modulates aging in C. elegans.

Authors:  Shanshan Pang; Sean P Curran
Journal:  Cell Metab       Date:  2014-01-16       Impact factor: 27.287

6.  Transcription Factor Activity Mapping of a Tissue-Specific in vivo Gene Regulatory Network.

Authors:  Lesley T MacNeil; Carles Pons; H Efsun Arda; Gabrielle E Giese; Chad L Myers; Albertha J M Walhout
Journal:  Cell Syst       Date:  2015-08-26       Impact factor: 10.304

7.  CONSERVED AND EXAPTED FUNCTIONS OF NUCLEAR RECEPTORS IN ANIMAL DEVELOPMENT.

Authors:  Shari Bodofsky; Francine Koitz; Bruce Wightman
Journal:  Nucl Receptor Res       Date:  2017

Review 8.  Control of Germline Stem Cell Lineages by Diet and Physiology.

Authors:  Kaitlin M Laws; Daniela Drummond-Barbosa
Journal:  Results Probl Cell Differ       Date:  2017

9.  Methodological considerations for heat shock of the nematode Caenorhabditis elegans.

Authors:  Shannin C Zevian; Judith L Yanowitz
Journal:  Methods       Date:  2014-04-26       Impact factor: 3.608

10.  Interspecies systems biology uncovers metabolites affecting C. elegans gene expression and life history traits.

Authors:  Emma Watson; Lesley T MacNeil; Ashlyn D Ritter; L Safak Yilmaz; Adam P Rosebrock; Amy A Caudy; Albertha J M Walhout
Journal:  Cell       Date:  2014-02-13       Impact factor: 41.582

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