SIngle-cell transcriptional networks during B cell differentiation
| Project/Area Number |
16K15506
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Hematology
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| Research Institution | Institute of Physical and Chemical Research |
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Principal Investigator |
Ikawa Tomokatsu 国立研究開発法人理化学研究所, 統合生命医科学研究センター, 上級研究員 (60450392)
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| Project Period (FY) |
2016-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥3,380,000 (Direct Cost: ¥2,600,000、Indirect Cost: ¥780,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2016: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | B細胞分化 / 1細胞発現解析 / 運命決定 / 転写因子 / 造血幹細胞 / B細胞 / 分化 / 1細胞 |
|---|
| Outline of Final Research Achievements |
B cells are generated from hematopoietic stem cells (HSCs) through a successive series of lineage restriction processes. Although many transcription factors were shown to control the B cell fate determination, the exact mechanisms remain largely unknown. We have recently established an ideal system that can be used to examine gene regulatory networks during lymphoid lineage commitment from HSCs. In this study, we focused on the gene expression profiles at the single cell level during B cell differentiation using this system. The single cell RNA-seq analysis using the in vitro culture system demonstrated the step-wise activation of B-lineage associated genes, whereas the genes involved in the multipotency were gradually repressed. The gene expression patterns obtained by the culture system totally fit with the data of the single progenitors isolated from mouse bone marrow. These results will provide a blueprint for studying the normal and neoplastic development of B cells.
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Report
(3 results)
Research Products
(20 results)
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[Journal Article] Three-step transcriptional priming that drives the commitment of multipotent progenitors toward B cells.2018
Author(s)
2.Miyai T, Takano J, Endo TA, Kawakami E, Agata Y, Motomura Y, Kubo M, Kashima Y, Suzuki Y, Kawamoto H, Ikawa T.
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Journal Title
Genes Dev
Volume: 32
Pages: 112-126
DOI
Related Report
Peer Reviewed / Int'l Joint Research
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[Journal Article] Conversion of T cells to B cells by inactivation of polycomb-mediated epigenetic suppression of the B-lineage program2016
Author(s)
Ikawa T, Masuda K, Endo TA, Endo M, Isono K, Koseki Y, Nakagawa R, Kometani K, Takano J, Agata Y, Katsura Y, Kurosaki T, Vidal M, Koseki H, Kawamoto H
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Journal Title
Genes & Development
Volume: 30
Pages: 2475-2485
Related Report
Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
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[Journal Article] Transient Tcf3 gene repression by TALE-tanscription factor targeting2016
Author(s)
Masuda J, Kawamoto H, Strober W, Takayama-E, Mizutani A, Murakami H, Ikawa T, Kitani A, Maeno N, Shigehiro T, Satoh A, Seno A, Arun V, Kasai T, Fuss IJ, Katsura Y, Seno M
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Journal Title
Appl Biochem Biotechnol
Volume: 180
Pages: 1559-1573
Related Report
Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
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