| Autor: |
Fox, Bennett W., Ponomarova, Olga, Lee, Yong-Uk, Zhang, Gaotian, Giese, Gabrielle E., Walker, Melissa, Roberto, Nicole M., Na, Huimin, Rodrigues, Pedro R., Curtis, Brian J., Kolodziej, Aiden R., Crombie, Timothy A., Zdraljevic, Stefan, Yilmaz, L. Safak, Andersen, Erik C., Schroeder, Frank C., Walhout, Albertha J. M. |
| Zdroj: |
Nature; July 2022, Vol. 607 Issue: 7919 p571-577, 7p |
| Abstrakt: |
Individuals can exhibit differences in metabolism that are caused by the interplay of genetic background, nutritional input, microbiota and other environmental factors1–4. It is difficult to connect differences in metabolism to genomic variation and derive underlying molecular mechanisms in humans, owing to differences in diet and lifestyle, among others. Here we use the nematode Caenorhabditis elegansas a model to study inter-individual variation in metabolism. By comparing three wild strains and the commonly used N2 laboratory strain, we find differences in the abundances of both known metabolites and those that have not to our knowledge been previously described. The latter metabolites include conjugates between 3-hydroxypropionate (3HP) and several amino acids (3HP-AAs), which are much higher in abundance in one of the wild strains. 3HP is an intermediate in the propionate shunt pathway, which is activated when flux through the canonical, vitamin-B12-dependent propionate breakdown pathway is perturbed5. We show that increased accumulation of 3HP-AAs is caused by genetic variation in HPHD-1, for which 3HP is a substrate. Our results suggest that the production of 3HP-AAs represents a ‘shunt-within-a-shunt’ pathway to accommodate a reduction-of-function allele in hphd-1. This study provides a step towards the development of metabolic network models that capture individual-specific differences of metabolism and more closely represent the diversity that is found in entire species. |
| Databáze: |
Supplemental Index |
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