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新規同定されたNH細胞におけるサイトカイン産生を制御する転写ネットワークの解明

Research Project

Project/Area Number 23710238
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field System genome science
Research InstitutionThe Institute of Physical and Chemical Research

Principal Investigator

BERTIN nicolas  独立行政法人理化学研究所, ライフサイエンス技術基盤研究センター, 研究員 (30525861)

Project Period (FY) 2011 – 2012
Project Status Discontinued (Fiscal Year 2011)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2012: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Fiscal Year 2011: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Keywordsgene networks / transcriptome / natural helper cell / sytokine / transcriptional network / CAGE / immune system / 遺伝子ネットワーク / 免疫 / トランスクリプトーム
Research Abstract

We proposed to characterize the transcriptional landscapes of naive, IL2+IL25 and IL33 activated NH cells. RNA from FACS-sorted cells were sequenced using helicosCAGE. The 2-10 million CAGE tags obtained were mapped and their 5'extremity representing Transcription Start Sites were clustered (TSS clusters) and associated with RefSeq transcripts. In parallel, our collaborators investigated IL33 induced signaling, uncovering the role of GATA3 (Furusawa etal. J Immunol. 2013), which we focused our attention on. We uncovered 36 stimulated NH cell-specific GATA3 targets. TSS clusters location, associations and expression levels are available via the ZENBU browser (Severin etal. Nat Biotech. Accepted) which serves for the dissemination of the FAMTOM5 project, in which this study was incorporated.

Report

(3 results)
  • 2013 Annual Research Report
  • 2012 Research-status Report
  • 2011 Research-status Report

URL: 

Published: 2011-08-05   Modified: 2019-07-29  

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