Functional relationship between cell fate decision and epigenetic control of gene expression of the chromosome
Project/Area Number |
26670465
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Hematology
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Research Institution | The University of Tokyo |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
INABA Toshiya 広島大学, 原爆放射線医科学研究所, 教授 (60281292)
MATSUI Hirotaka 熊本大学, 大学院生命科学研究部, 教授 (60379849)
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Project Period (FY) |
2014-04-01 – 2016-03-31
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Project Status |
Completed (Fiscal Year 2015)
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Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | エピジェネティクス / 細胞分化 / ヒストン修飾 / スプライシング / 好中球 |
Outline of Final Research Achievements |
A human leukemic cell line HL60 differentiates to granulocytes and monocytes in response to retinoic acid and vitamin D3 treatment, respectively. In this project, we performed RNAseq analysis serially, and searched genes whose expression increases during the differentiation processes. In the results, we have identified several such genes. However, in contrast to our prediction, these genes do not localize in the neighborhood of chromosomes. Therefore, to investigate the roles of epigenetics in the differentiation of HL60 cells, we next knocked down an epigenetic factor ASXL1 involved in histone modification and analyzed the relationship between cell differentiation and histone modification. We have found that ASXL1 knockdown decreases trimethylation of histone H3K4 and H3K27 leading to inhibition of the differentiation of HL60 cells.
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Report
(3 results)
Research Products
(17 results)
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[Journal Article] Novel working hypothesis for pathogenesis of hematological malignancies: combination of mutations-induced cellular phenotypes determines the disease (cMIP-DD).2016
Author(s)
Kitamura T, Watanabe-Okochi N, Enomoto Y, Nakahara F, Oki T, Komeno Y, Kato N, Doki N, Uchida T, Kagiyama Y, Togami K, Kawabata KC, Nishimura K, Hayashi Y, Nagase R, Saika M, Fukushima T, Asada S, Fujino T, Izawa Y, Horikawa S, Fukuyama T, Tanaka Y, Ono R, Goyama S, Nosaka T, Kitaura J, Inoue D
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Journal Title
Journal of Biochemistry
Volume: 159
Issue: 1
Pages: 17-25
DOI
Related Report
Peer Reviewed / Int'l Joint Research
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[Journal Article] A C-terminal mutant of CCAAT-enhancer-binding protein α (C/EBPα-C(m)) downregulates Csf1r, a potent accelerator in the progression of acute myeloid leukemia with C/EBPα-C(m).2015
Author(s)
Togami K, Kitaura J, Uchida T, Inoue D, Nishimura K, Kawabata KC, Nagase R, Horikawa S, Izawa K, Fukuyama T, Nakahara F, Oki T, Harada Y, Harada H, Aburatani H, Kitamura T.
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Journal Title
Exp Hematol.
Volume: 43(4)
Issue: 4
Pages: 300-308
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] SETBP1 mutations drive leukemic transformation in ASXL1-mutated MDS.2015
Author(s)
Inoue D, Kitaura J, Matsui H, Hou HA, Chou WC, Nagamachi A, Kawabata KC, Togami K, Nagase R, Horikawa S, Saika M, Micol JB, Hayashi Y, Harada Y, Harada H, Inaba T, Tien HF, Abdel-Wahab O, Kitamura T.
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Journal Title
Leukemia
Volume: 29(4)
Issue: 4
Pages: 847-57
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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