| Project/Area Number |
23790073
|
|---|
| Research Category |
Grant-in-Aid for Young Scientists (B)
|
| Allocation Type | Multi-year Fund |
|---|
| Research Field |
Biological pharmacy
|
|---|
| Research Institution | Tohoku University |
|---|
Principal Investigator |
|
|---|
| Research Collaborator |
KURATA Shoichiro 東北大学, 大学院・薬学研究科, 教授 (90221944)
|
|---|
| Project Period (FY) |
2011 – 2012
|
| Project Status |
Completed (Fiscal Year 2012)
|
| Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2011: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
|---|
| Keywords | 自然免疫 / 遺伝子発現制御 / エピジェネティクス |
|---|
| Research Abstract |
To identify novel, evolutionally conserved epigenetic mechanisms that regulate gut immunity or homeostasis, we explored chromatin modifiers involved in intestinal pathology using the Drosophila model system. We found that forced removal of histone H3 lysine36 methylation (H3K36me) in intestinal stem cell (ISC)/enteroblast (EB) increases the resistance to Pseudomonas aeruginosa infection. However, further analyses indicated that the forced H3K36me demethylation in ISC/EB causes over-activation of oxidative stress response genes and shortens lifespan. These results suggest that H3K36me might contribute to appropriate regulation of stress responses and/or the maintenance of homeostasis in Drosophila intestine.
|
