| Literature DB >> 29587144 |
Fumiaki Obata1, Kayoko Tsuda-Sakurai2, Takahiro Yamazaki2, Ryo Nishio2, Kei Nishimura2, Masaki Kimura2, Masabumi Funakoshi2, Masayuki Miura3.
Abstract
The intestine has direct contact with nutritional information. The mechanisms by which particular dietary molecules affect intestinal homeostasis are not fully understood. In this study, we identified S-adenosylmethionine (SAM), a universal methyl donor synthesized from dietary methionine, as a critical molecule that regulates stem cell division in Drosophila midgut. Depletion of either dietary methionine or SAM synthesis reduces division rate of intestinal stem cells. Genetic screening for putative SAM-dependent methyltransferases has identified protein synthesis as a regulator of the stem cells, partially through a unique diphthamide modification on eukaryotic elongation factor 2. In contrast, SAM in nutrient-absorptive enterocytes controls the interleukin-6-like protein Unpaired 3, which is required for rapid division of the stem cells after refeeding. Our study sheds light upon a link between diet and intestinal homeostasis and highlights the key metabolite SAM as a mediator of cell-type-specific starvation response.Entities:
Keywords: Drosophila; JAK/STAT; S-adenosylmethionine; diphthamide; intestinal stem cell; methionine; methylation; nutrient; starvation; translation
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Year: 2018 PMID: 29587144 DOI: 10.1016/j.devcel.2018.02.017
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270