Team Leader
Fumiaki Obata
Ph.D.
Laboratory for Nutritional Biology
LocationKobe / Developmental Biology Buildings
E-mailfumiaki.obata[at]riken.jp
Please replace [at] with @.
The organismal healthspan is significantly influenced by the quality and quantity of the diet, but our understanding of the detailed molecular mechanisms remains limited. Diet contributes to the metabolic and physiological homeostasis of animals directly as nutrients or indirectly via gut microbiome, but a detailed understanding of the molecular mechanisms is lacking. In our laboratory, we study the physiological functions of various nutrients and gut bacteria during each life stage, including development, growth, reproduction, and aging, as well as the adaptation mechanisms of animals to nutritional over- and undernutrition. We are also trying to elucidate the mechanisms by which transient dietary intake during development and development influences health status throughout life.
Research Themes
- Lifespan Extension through Dietary Restriction
- Specific Sensing of Nutrients and the Adaptive Mechanism to their Deficiency
- Function of gut microbiome and diet-microbiome-host interactions
- Healthspan changes by early-life dietary environment
- Blood-feeding Behaviour and Metabolic Homeostasis in Mosquitoes
- Nutrition, Physiology, and Metabolism in Primates
Selected Publications
Kosakamoto H, Sakuma C, Okada R, et al.
Context-dependent impact of the dietary non-essential amino acid tyrosine on Drosophila physiology and longevity.
Science Advances
10(35), eadn7167 (2024)
doi: 10.1126/sciadv.adn7167
Sakuma C, Iwamoto T, Masuda K, et al.
Fibrinopeptide A-induced blood-feeding arrest in the yellow fever mosquito Aedes aegypti.
Cell Reports
(2024)
doi: 10.1016/j.celrep.2024.114354
Kosakamoto H, Miura M, Obata F.
Epidermal tyrosine catabolism is crucial for metabolic homeostasis and survival against high-protein diets in Drosophila.
Development
151(1), dev202372 (2024)
doi: 10.1242/dev.202372
Kosakamoto H, Obata F, Kuraishi J, et al.
Early-adult methionine restriction reduces methionine sulfoxide and extends lifespan in Drosophila.
Nature Communications
14(1), 7832 (2023)
doi: 10.1038/s41467-023-43550-2
Onuma T, Yamauchi T, Kosakamoto H, et al.
Recognition of commensal bacterial peptidoglycans defines Drosophila gut homeostasis and lifespan.
PLOS Genetics
19(4), e1010709 (2023)
doi: 10.1371/journal.pgen.1010709
Kosakamoto H, Okamoto N, Aikawa H, et al.
Sensing of the non-essential amino acid tyrosine governs the response to protein restriction in Drosophila.
Nature Metabolism
4(7), 944-959 (2022)
doi: 10.1038/s42255-022-00608-7
Yamauchi T, Oi A, Kosakamoto H, et al.
Gut Bacterial Species Distinctively Impact Host Purine Metabolites during Aging in Drosophila.
iScience
23, 101477 (2020)
doi: 10.1016/j.isci.2020.101477
Kosakamoto H, Yamauchi T, Akuzawa-Tokita Y, et al.
Local Necrotic Cells Trigger Systemic Immune Activation via Gut Microbiome Dysbiosis in Drosophila.
Cell Reports
32(3), 107938 (2020)
doi: 10.1016/j.celrep.2020.107938
Obata F, Tsuda-Sakurai K, Yamazaki T, et al.
Nutritional Control of Stem Cell Division through S-Adenosylmethionine in Drosophila Intestine.
Developmental Cell
44(6), 741-751 (2018)
doi: 10.1016/j.devcel.2018.02.017
Obata F, Fons CO, Gould AP.
Early-life exposure to low-dose oxidants can increase longevity via microbiome remodelling in Drosophila.
Nature Communications
9(1), 975 (2018)
doi: 10.1038/s41467-018-03070-w
News
Mar. 26, 2024 Research
Flies fed restricted diet in early adulthood live longer
Mar. 15, 2024 BDR News
Dive into BDR's intriguing research
The Desire to Explain Nutrition Properly
Jul. 28, 2023 Research
How a gut microbe causes flies to live fast and die young
Oct. 17, 2022 Research
‘Non-essential’ building block proves vital to a healthy protein diet
Apr. 12, 2021 BDR News
Five new laboratories join RIKEN BDR